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mid<br />

<strong>Remineralization</strong> <strong>with</strong> <strong>CPP</strong>-<strong>ACP</strong>:<br />

minimum intervention, maximum return<br />

the evidence<br />

Hands on,<br />

drills off<br />

Remineralisation <strong>with</strong> <strong>CPP</strong>-<strong>ACP</strong>’ to MIH:<br />

the treatment protocol<br />

Remineralisation<br />

<strong>with</strong> <strong>CPP</strong>-<strong>ACP</strong><br />

MID<br />

resources<br />

Issue 3


Prevention starts <strong>with</strong><br />

risks identification<br />

and personal motivation<br />

Plaque Indicator Kit from <strong>GC</strong>.<br />

Identify plaque cariogenicity and age <strong>with</strong>in 5 minutes<br />

<strong>GC</strong> EUROPE N.V.<br />

Head Office<br />

Tel. +32.16.74.10.00<br />

info@gceurope.com<br />

www.gceurope.com<br />

<strong>GC</strong> UNITED KINGDOM Ltd.<br />

Tel. +44.1908.218.999<br />

info@uk.gceurope.com<br />

www.uk.gceurope.com<br />

Plaque formation is a<br />

normal occurrence for<br />

most of the population.<br />

To determine the potential<br />

damage plaque can cause<br />

and discover exactly which<br />

plaque sites are more<br />

problematic than others can<br />

be difficult to identify.<br />

Plaque Indicator Kit is a simple and<br />

inexpensive test that quickly identifies<br />

and visually communicates the problem<br />

to motivate and educate patients.<br />

Minimum<br />

Intervention


minimum intervention, maximum return<br />

What’s inside<br />

MID 3 video<br />

4. MID Worldwide<br />

mid<br />

Issue 3<br />

Thanks to the cooperation of academia, the profession and industry leadership<br />

by <strong>GC</strong>, Minimum Intervention Dentistry principles are adopted and promoted<br />

around the world, to the ultimate bene t of the patient community.<br />

6. Q&A<br />

Dr Graham Mount answers a question about what he has found to be the most<br />

e ective way to apply <strong>CPP</strong>-<strong>ACP</strong><br />

7. Resources<br />

Networks, websites, books, events and journal articles relating<br />

to advances in MID<br />

8. Practice perspectives<br />

• Hands on, drills off<br />

10. Clinical corner<br />

• MIH: the evidence and treatment protocol<br />

• White spot reversal protocol<br />

• Topical <strong>CPP</strong>-<strong>ACP</strong> crème (Tooth Mousse): more evidence<br />

that demands a verdict<br />

26. Evidence<br />

• A closer look at remineralisation and <strong>CPP</strong>-<strong>ACP</strong><br />

30. MI toolkit<br />

• Tooth Mousse: All you need to know<br />

mi.gceurope.com


worldwide<br />

MID Worldwide<br />

Thanks to the cooperation of academia, the profession and industry leadership<br />

by <strong>GC</strong>, Minimum Intervention Dentistry principles are adopted and promoted<br />

around the world, to the ultimate bene t of the patient community.<br />

Dr Matteo Basso<br />

As a student, I did my internship in<br />

the Department of Periodontology<br />

at the University of Milan, directed by<br />

Professor Roberto Weinstein. In that<br />

department, the concepts of minimally<br />

invasive dentistry had been rmly<br />

ingrained for many years and advanced periodontal<br />

procedures were envied and admired nationally and<br />

internationally. Here I learnt the importance of the<br />

preservation of healthy tissue as a fundamental condition<br />

for the success of treatment, both functionally and<br />

aesthetically. After graduation and obtaining a PhD, I<br />

became the head of restorative dentistry at the university<br />

dental clinic, IRCCS Galeazzi Orthopaedic Institute<br />

in Milan (Italy). There, I realized it was a good approach<br />

to change concepts of minimally invasive therapy,<br />

Italy MID<br />

possible only when a disease is already established,<br />

towards the concept of ‘minimum intervention’, in other<br />

words to intervene when the disease has not yet had an<br />

irreversible e ect on the teeth and gums.<br />

The literature helped us to comprehend what ‘minimum<br />

intervention’ actually is. And so, the traditional<br />

department of restorative dentistry quickly evolved<br />

into a new department, built on these ideas, called the<br />

Center of Aesthetic and Mininvasive Oral Rehabilitation<br />

(CROME). The goal of this centre is to intervene early in<br />

carious disease, seeking not only to treat cavities, however<br />

necessary, but also to understand why the carious<br />

lesions manifested themselves in the rst place. One of<br />

our challenges is to see if you can change the susceptibility<br />

of patients in order to protect their teeth and masticatory<br />

ability. It was not so easy to explain to patients<br />

all the reasons and the importance of this approach,<br />

4 mid worldwide<br />

mi.gceurope.com


China<br />

but after several years, we can say that the programme<br />

is a big success in tooth preservation. To create a form of<br />

restorative dentistry that can prevent the intervention of<br />

the periodontist, the prosthodontist or implantologist for<br />

as long as possible is the main goal for me and my sta .<br />

The adoption of the MID, once understood, is very<br />

simple. However, we cannot hide that the rst and biggest<br />

challenge is the identi cation of clear guidelines for the<br />

correct application of MID into the clinical reality of each<br />

dentist. Still too many dentists observe the magni cent<br />

results of some colleagues who publish books and<br />

magazines on MID, but still wonder how they can integrate<br />

it into their own situations. Some are even afraid to make<br />

the patients pay for preventive diagnostic procedures, and<br />

therefore they prefer not to perform diagnosis and tests,<br />

intervening when there is already an established disease<br />

or, even worse, when the disease can be only treated<br />

Dr Zhouqun Yan, <strong>GC</strong> China<br />

There is an increasing awareness of MI among the Chinese<br />

dental profession. This is due to information in international<br />

journals and returning overseas dentists who have studied<br />

abroad for postgraduate degrees or special research projects.<br />

However, due to the requirement of an import license for any<br />

item regarded as a dental device, most ‘state of the art’ items<br />

including MI products are not available for Chinese dentists at the same time as<br />

other countries. Some successful items take years to satisfy the strict governmental<br />

requirements. To emphasise this, Tooth Mousse was only launched in China at<br />

the end of 2009. At present, most of the products available in China t into the<br />

repair category of the MI concept and products like <strong>GC</strong> Fuji IX GP are popular in<br />

government dental clinics. It is di cult to embrace the complete MI concept in<br />

the majority of government clinics at this stage but private dentists have already<br />

realized the MI concept of diagnosis, prevention and repair is the future.<br />

In the large cities like Beijing and Shanghai, it is possible to run a successful<br />

dental practice based on MI principles. However, more information and education<br />

about MI is the key to boost the concept in these cities.<br />

<strong>GC</strong> Fuji IX GP is the bestselling MI product in China and complies <strong>with</strong> the<br />

‘easier, faster and better’ concept of Dr Gordon Christensen and other leading<br />

clinicians around the world. Economic reasons dictate that only the hand-mix<br />

version of Fuji IX GP is popular here. This special high strength glass ionomer<br />

has changed the way dentists work throughout China. It is also important to<br />

understand that China is a developing country and the ART technique is very<br />

important in remote areas. <strong>GC</strong> is working together <strong>with</strong> local KOLs and government<br />

departments to boost the availability of ART there. Fuji IX GP is the key to<br />

the success in these areas and overall sales have doubled over the past 2 years.<br />

MI dentistry is the future. It is not only a <strong>GC</strong> story but the future for the<br />

dental profession everywhere in the world. It is not something that costs extra<br />

money but can help dentists earn more. MI will eventually reduce costs for<br />

patients if they are also educated in proper oral care and embrace the principles<br />

as there will be less invasive treatment necessary. One of the exciting long<br />

term projects will be to work <strong>with</strong> policymakers to train dental professionals to<br />

identify and heal early lesions rather than watch and wait for them to progress<br />

to cavitation. MI will mean that dentists and nurses will be busier than ever but<br />

<strong>with</strong> many new and di erent roles in the practice.<br />

conservatively <strong>with</strong> the ‘drill, ll and bill’ option.<br />

Sometimes dentists are not helped by di erent<br />

situations in <strong>Europe</strong>an countries: for example, in some<br />

countries there is no profession of the dental hygienist,<br />

a role in other countries which is championing the MID<br />

drive. The MID principles are certainly not so easy to<br />

introduce immediately into clinical daily practice, because<br />

it requires dentists to evaluate their own resources<br />

(sta , hygienist, number of dental chairs, availability of<br />

patients) and sometimes to signi cantly change their<br />

habits of diagnosis and treatments.<br />

Minimum intervention dentistry is a eld that is in<br />

continuous expansion. Its potential results, in terms of<br />

successful treatment <strong>with</strong> aesthetic success and conservation<br />

of the masticatory function, are huge compared<br />

to its di usion, which is unfortunately still small <strong>with</strong>in<br />

the national territory.<br />

mid worldwide<br />

5


Q&A<br />

The question below was sent to<br />

Dr Graham Mount in response<br />

to his article in MID 2<br />

Name: Jack Stellpflug<br />

Country: USA<br />

Question: Can Dr Mount comment on the most effective way he has found to apply CCP-<strong>ACP</strong>?<br />

Answer – Dr Graham Mount<br />

Dear Jack Stellpflug,<br />

The material CCP-<strong>ACP</strong>, developed in Melbourne, came from a desire to be able to<br />

remineralise a demineralised enamel or dentine lesion in depth. As you are aware the<br />

application of fluoride in one form or another will tend to remineralise the surface<br />

first and will tend to prevent the further penetration of ions in to the depths of the<br />

lesion. This may well minimize the further demineralisation of the area but it will not<br />

overcome the level of porosity of the tooth structure in depth. In other words a ‘white<br />

spot lesion’ may well remain visible to the naked eye even though the lesion is sealed<br />

from further loss of ions in the short term.<br />

On the other hand the <strong>CPP</strong>-<strong>ACP</strong> will penetrate to the full depth of the<br />

demineralisation and will successfully deposit both calcium and phosphate ions to<br />

the full depth of the lesion thus overcoming the ‘white spot’ entirely. Add the fluoride<br />

ion to it and the resistance to further demineralisation will be further enhanced – that<br />

is, use Tooth Mousse Plus.<br />

This means that the preferred timing and method of application will be to apply<br />

when the disease is first diagnosed and before any other fluoride therapy has<br />

been introduced. The most effective way is to make a personal plastic ‘pull-down’<br />

specifically for the patient. Apply daily, carry out normal hygiene then apply pulldown<br />

loaded <strong>with</strong> <strong>CPP</strong>-<strong>ACP</strong> paste and leave in place for say 15 minutes on each<br />

occasion. Treatment may need to last for 2 weeks or thereabouts, longer if desired.<br />

As part of an overall anti-caries discipline for the high risk patient or one <strong>with</strong> cervical<br />

sensitivity it can also be applied <strong>with</strong> the finger after cleaning any time and leave it<br />

on the teeth for as long as you like. It will wash away quite quickly of course but in<br />

the meantime will have transferred a reasonable dose of ions to the dentine beneath<br />

assisting in closing over the tubules.<br />

Yours sincerely,<br />

Graham Mount<br />

Melbourne, Australia<br />

6 q&a<br />

mi.gceurope.com


MID resources<br />

This is a collection of online resources on MID for dental professionals and patients<br />

Online<br />

Dental Village<br />

Dentalvillage is an online resource developed my two dental hygienists,<br />

Dave Bridges and Tim Ives who are passionate about raising the profi le<br />

of MID among the public and healthcare professions. The site has up<br />

to date information on this fresh approach to preventing dental decay<br />

and periodontal (gum) diseases.<br />

Excerpt: The focus is on maximum conservation of demineralised, noncavitated<br />

enamel and dentine. Once control of the infection is achieved,<br />

the patient’s caries risk status and evidence of lesion demineralisation<br />

can be monitored over extended periods. These principles can also<br />

be applied to the treatment and management of periodontal disease.<br />

Minimally Invasive Periodontal Management relies heavily on patient<br />

involvement, ownership and management of their own disease. The<br />

patient reduces their own infl ammation under guidance of the clinician<br />

and operative treatment is kept as minimal as possible.<br />

Click here: dentalvillage.co.uk<br />

Dental Caries Classi cation Grid<br />

An online resource run by Graham Mount, Wyatt Rory Hume and<br />

Brian Monteith has an interactive dental caries classifi cation grid<br />

based on MID principles that introduces an alternative to the GV Black<br />

classifi cation system.<br />

Excerpt: A revised understanding of the caries lesion<br />

In recent times the term “Minimal Intervention Dentistry” has been<br />

coined to describe a new approach to the treatment of early carious<br />

lesions. It is now clearly acknowledged that caries is a bacterial disease<br />

and treatment should therefore revolve primarily around overcoming<br />

the infection.<br />

Click here: http://www.midentistry.org/grid.html<br />

California Dental Association Journal Back Issues<br />

The California Dental Association has made the back issues of its journal<br />

available for download online through its website.<br />

Excerpt: The Journal of the California Dental Association is an awardwinning<br />

monthly peer-reviewed scientifi c publication keeps dentists<br />

up-to-date about scientifi c advances, business management strategies<br />

and new products. It also features thought-provoking editorials,<br />

comprehensive statewide continuing education listings, California<br />

practices for sale, and dentistry’s favourite humour columnist - Dr Bob,<br />

Robert E. Horseman, DDS.<br />

Click here: http://www.cda.org/publications/journal_of_the_<br />

california_dental_association<br />

MID patient factsheet<br />

Academy of General Dentistry has compiled a useful document that<br />

explains the principles of MID to patients<br />

Click here: http://www.midentistry.com/AGD-MI.pdf<br />

Professor Brian Nový articles<br />

Professor Nový is featured in the USA<br />

version of the MID ezine, compiled by <strong>GC</strong><br />

America – click here to read the issue<br />

He is a renowned MID advocate and<br />

here is a list of some of his most recent<br />

publications:<br />

The Material Science of Minimally<br />

Invasive Restorations. Compendium of<br />

Continuing Education in Dentistry, July<br />

2008.<br />

Salivary Diagnostics: Practical<br />

Applications. AGD Impact. September 2009.<br />

Glass ionomers: Invaluable materials in<br />

today’s dental operatory. National Network<br />

for Oral Health Access Quarterly Newsletter.<br />

Winter 2009: 2(1).<br />

Profi le in Oral Health: Treating the Caries<br />

Disease, an interview <strong>with</strong> Dr. Brian B. Nový.<br />

Dental Town Magazine. April 2009 10(4):<br />

90-94.<br />

Dental Caries: A pH mediated disease.<br />

Journal of the California Dental Hygienist’s<br />

Association, Winter 2010: 25(1).<br />

Social media<br />

Here is an overview of MID related resources<br />

that you can follow through social media<br />

Facebook<br />

MI Paste (Tooth Mousse) fanpage<br />

Click here: http://www.facebook.com/#!/<br />

mi.paste?ref=ts<br />

Twitter<br />

MI Paste (Tooth Mousse)<br />

Click here: http://twitter.com/mipaste<br />

Carifree<br />

Click here: http://twitter.com/CariFree<br />

resources<br />

7


Hands on, drills off<br />

Dr Kirk Young is the practice principal and owner of Young’s Dental Practice, which was<br />

awarded the 2009 Preventive Practice of the Year award. MID recently spoke to him about his<br />

practice and what motivates him to pursue MID.<br />

“I always<br />

preferred<br />

doing<br />

prevention<br />

rather than<br />

extractions<br />

anyway”<br />

MID: What goes into achieving the title of<br />

Preventive Practice of the Year?<br />

Dr Kirk Young: According to the judges<br />

of this award, our dedication to improving<br />

patient care, passion and enthusiasm for MID<br />

in our practice is evident. In our practice we<br />

also have a physiotherapy and sports injury<br />

clinic and this all contributes to us being an<br />

overall preventive practice. An essential part<br />

of our success is excellent teamwork: from the<br />

reception staff, the nurses to the hygienists<br />

and dentists.<br />

The MI systems, materials and techniques<br />

that we have put in place at the practice<br />

have taken us many years to implement fully<br />

and we have spent a great deal of time and<br />

consideration on each. It certainly didn’t<br />

happen overnight!<br />

Years ago I was looking for a mentor in<br />

dentistry to inspire me. I met Hien Ngo at<br />

a conference and heard him speak quite<br />

a few times and his ideas influenced me<br />

tremendously. I always preferred doing<br />

prevention rather than extractions anyway.<br />

Another move in the right direction came<br />

when we stopped being an NHS practice<br />

four years ago. When the new NHS contract<br />

was announced I realised that the prevention<br />

component was not included. I felt we couldn’t<br />

give patients adequate care in prevention on<br />

the NHS so we became a private practice.<br />

We told the patients what was happening<br />

and why we were changing and they<br />

had already become used to our way of<br />

performing preventive dentistry. We always<br />

try to keep the patients involved – our<br />

website has many resources on MID and<br />

prevention for them.<br />

Winning the award has been a great<br />

recognition for the whole team and confirmed<br />

to us that what we are doing <strong>with</strong> MID and<br />

prevention is the way forward.<br />

MID: What techniques and strategies have<br />

you found to work best for doing preventive<br />

dentistry?<br />

Dr Kirk Young: Keeping patients informed<br />

is crucial. We have to show them what we<br />

have to offer and we do this through our<br />

newsletter, which every patient receives at a<br />

recall appointment. In it we publish content<br />

about the benefits of MID and prevention,<br />

and we highlight the equipment that helps<br />

us to practice preventively, such as Cariescan,<br />

The Wand, Healozone and Velopex.<br />

Using an intraoral camera is another<br />

excellent way get the patient involved in the<br />

problem. You don’t just tell them they have a<br />

disease, but you also show them where it is,<br />

how it looks and what it is doing. One of the<br />

cornerstones of MID is that it’s not a one way<br />

partnership between the patient and dentist.<br />

You need increased patient involvement to<br />

make this work.<br />

Education the team is another important<br />

facet and we have spent a great deal of time<br />

training together <strong>with</strong> the whole team. When<br />

the team members fully understand the<br />

8 practice perspectives<br />

mi.gceurope.com


enefits of MID they can explain it better to<br />

the patients and communicate the benefits<br />

more effectively to them.<br />

We also make use of questionnaires and<br />

work through these <strong>with</strong> the patients, in order<br />

to assess their caries risk. Our staff members<br />

are fully trained to undertake this because we<br />

find that sometimes the patients feel more<br />

comfortable to share this kind of information<br />

<strong>with</strong> the staff members. Everyone is focused on<br />

the practice having healthy and happy patients.<br />

MID: To what extent do you conduct practice<br />

based research in MID topics?<br />

Dr Kirk Young: Everything is recorded<br />

in our practice. Every patient fills out a<br />

comprehensive MID questionnaire, which<br />

is evaluated at every recall to see what<br />

treatment has worked or to monitor the<br />

progress. Our practice management software<br />

allows us to record all this data so we can<br />

chart the patient’s progress at each recall. At<br />

every appointment we measure the caries<br />

risk using the ‘traffic light system’ which is<br />

determined by using the intra-oral camera<br />

and questionnaires. All the oral hygiene and<br />

dietary advice given to each patient is also<br />

recorded to we can track their behaviour.<br />

Last year my practice data was used by Dr<br />

Avijit Banerjee at a conference presentation.<br />

I think it’s important to not only practice MID<br />

but to record and capture how we are treating<br />

patients so we can build the evidence base.<br />

MID: What advice would you give dentists<br />

who are considering moving over to an MIDcentered<br />

practice model?<br />

Dr Kirk Young:<br />

• Invest in team building and training.<br />

• Teach patients to self-prevent tooth decay<br />

proactively, rather than treating it reactively<br />

• Build your practice systems up gradually<br />

• Go to talks, attend courses <strong>with</strong> your team,<br />

join study groups; try to get as much<br />

information about MID as you can.<br />

• Invest in dental caries detection systems<br />

such as Diagnodent, Cariescan, SapproLife<br />

and use them every day<br />

• Make use of remineralisation products – they<br />

have a huge body of evidence behind them<br />

that support their efficacy<br />

• Keep on top of new developments: Air<br />

abrasion is another emerging aspect to MID<br />

- new research shows that bioactiveglass<br />

material can cut through enamel very<br />

quickly and can kickstart the reminerlisation<br />

process in the teeth<br />

I am still surprised to see how few dentists<br />

have intraoral cameras in their practices. In<br />

some countries this is second nature. I hope<br />

to see this change in the UK. MID is the<br />

buzzword in dentistry at the moment, it is no<br />

longer a marginal activity, everyone is talking<br />

about it. It is the way forward for dentistry<br />

For more information about the practice visit<br />

www.youngsdentalpractice.co.uk<br />

A day in the life at Young’s Dental Practice<br />

Sally Wright, practice manager<br />

I enjoy most being part of a team who are all working towards the same goal - for all clients to be<br />

dentally fit etc. I also enjoy organising Kirk’s lectures and taking part in them and co-ordinating<br />

<strong>with</strong> the dental companies supporting MID. I probably gain most enjoyment from patient<br />

interaction especially when involving them in their care which includes oral health, diet and<br />

grinding advice.<br />

My specific roles include educating patients by oral hygiene instruction and diet advice,<br />

grinding appliance demonstration and advice. I also give patients information on the techniques<br />

and equipment we use such as air abrasion for MID. I am responsible for doing MID marketing by creating leaflets,<br />

website updates and brochures. I help <strong>with</strong> MID lectures and discussions <strong>with</strong> GDPs / VDPs and I advise patients on<br />

different most up to date products to assist them at home in prevention.<br />

I think we have been so successful as a team because we are all big believers in MID. We also spend a large<br />

amount of time <strong>with</strong> our patients implementing MID and great part of it is education. We also use intra-oral cameras<br />

routinely for examinations and patients are offered separate time <strong>with</strong> a DCP for any advice.<br />

practice perspectives<br />

9


MIH: the evidence and treatment protocols<br />

By Dr Felicity Crombie and Dr David Manton<br />

While developmental defects have long been<br />

identified in human enamel, recently a new condition<br />

has been described: molar incisor hypomineralisation<br />

(MIH). First suggested as a distinct diagnosis by<br />

Weerheijm et al in 2001 it is defined as demarcated,<br />

qualitative defects of enamel (hypomineralisation) of<br />

systemic origin of one to four permanent first molars,<br />

frequently associated <strong>with</strong> affected incisors 1. Given<br />

the propensity of affected molars to break down<br />

rapidly and/or develop caries there is some debate<br />

as to whether this condition constitutes a new entity<br />

or has simply become more apparent as caries rates<br />

decrease and accurate diagnosis improves, both in<br />

regards to differentiating between true hypoplasia<br />

and post-eruptive breakdown (PEB) and recognition<br />

of abnormal caries patterns/presentation. The<br />

distribution of the condition is often asymmetric,<br />

<strong>with</strong> marked variation in severity common <strong>with</strong>in an<br />

individual. The likelihood that incisors are affected<br />

has been reported to increase as the number and<br />

severity of molar lesions increases 2 .<br />

Affected teeth present patients and clinicians<br />

alike <strong>with</strong> many challenges <strong>with</strong> aesthetic issues,<br />

hypersensitivity, difficulty achieving adequate local<br />

analgesia and difficulty providing adequate and<br />

enduring restorations all reported in association <strong>with</strong><br />

MIH1,3. Children <strong>with</strong> teeth affected by MIH undergo<br />

up to ten times the treatment of unaffected children<br />

by the age of 8 years and have significantly higher<br />

levels of dental anxiety<br />

and phobia 4,5. These<br />

factors combined<br />

<strong>with</strong> the<br />

fact that extraction is often the most appropriate<br />

definitive treatment option means general<br />

anaesthetic management, <strong>with</strong> its attendant increase<br />

in risk and cost, is often required 6-8.<br />

Prevalence<br />

Prevalence studies are increasingly investigating MIH<br />

specifically and using newly developed indices tailored<br />

for this purpose 9,10 ; however the majority of published<br />

studies have used either non-standard indices or<br />

the Developmental Defects of Enamel (DDE) Index.<br />

Caution must therefore be applied when interpreting<br />

prevalence data as the DDE Index has the potential to<br />

both over- and under- estimate the true prevalence<br />

of MIH since: MIH is not the only cause of demarcated<br />

enamel defects; caries, PEB, restoration and extraction<br />

are not accounted for by the DDE Index and PEB may<br />

be classified incorrectly as hypoplasia.<br />

A recent review of MIH prevalence data found that<br />

the prevalence varied widely <strong>with</strong> values from 2.4%<br />

to 40.2% reported11. The majority of studies were<br />

performed using <strong>Europe</strong>an populations and ranged<br />

from 2.4% in Germany and Bulgaria to 37.5% in<br />

Denmark. Worldwide a low prevalence has been<br />

reported in Hong Kong (2.8%) and Libya (2.9%)<br />

increasing to 13.7% in Kenya, 22% in Australia<br />

and up to 40.2% in Brazil. The lack of standardized<br />

examination protocols as well as the aforementioned<br />

index limitations must be considered when<br />

comparing these results. Although difficult to<br />

establish given the lack of reliable, comparable<br />

prevalence data worryingly many clinicians feel the<br />

prevalence of MIH is increasing3, 12.<br />

Aetiological factors<br />

The limitations of experimental design and study<br />

comparability identified for prevalence data also<br />

apply to a review of MIH aetiology. Bearing this in<br />

mind a critical literature review found: very little<br />

evidence to support a relationship between<br />

breast-feeding or fluoride exposure and<br />

demarcated enamel defects; moderate<br />

evidence that exposure to PCB/dioxins may<br />

be associated <strong>with</strong> an increased prevalence<br />

of these lesions; maternal factors, birth<br />

complications, nutritional status, childhood<br />

illness and medical conditions appear to<br />

exert some influence on the prevalence<br />

of enamel defects generally, but the type of<br />

defect and the specific aetiological factors<br />

are not yet clear 13 . It is also likely that, in<br />

addition to the environmental exposures<br />

so far identified, genetic susceptibility may<br />

10 clinical corner<br />

mi.gceurope.com


the disease itself, the associated fever, the treatment<br />

administered or a combination which is responsible 14.<br />

Tooth properties<br />

As <strong>with</strong> the clinical presentation of MIH, lesions<br />

studied in vitro are often highly variable, however<br />

some significant findings for enamel affected by MIH<br />

include: increased porosity; decreased hardness;<br />

decreased mineral content; increased carbonate<br />

content; increased protein content and abnormal<br />

ultrastructure, etching patterns and bonding<br />

properties. Discrete areas of >25% porosity have<br />

been observed, though the bulk of lesions are less<br />

than 10%. Both microhardness and nanohardness<br />

is significantly reduced (up to a 70% reduction) as<br />

is mineral content (> 45% decrease) compared to<br />

normal enamel 15-17 . For both hardness and mineral<br />

content the gradient is abnormal <strong>with</strong> harder and<br />

more mineralised enamel found toward the dentinoenamel<br />

junction 16,17. For each of these properties the<br />

most severe areas are almost always in the outer half<br />

of enamel and a surface layer of reduced porosity and<br />

increased hardness and mineral content is observed,<br />

even in areas <strong>with</strong> PEB, while cervical regions appear<br />

unaffected. Higher carbon levels have been reported<br />

using secondary ion mass spectrometry which can<br />

reflect either a higher proportion of carbonated<br />

apatite or increased organic component 18 : in fact<br />

it appears to be a combination, <strong>with</strong> MIH lesions<br />

containing 3-15 times the protein (primarily<br />

exogenous) and 1.6 times the carbonate content of<br />

normal enamel 14,19.<br />

The ultrastructure of the enamel, observed under<br />

scanning electron microscopy (SEM) is also affected<br />

<strong>with</strong> increased disorganisation, abnormal prism<br />

core and inter-prismatic appearance and abnormal<br />

etching patterns reported 20,21 . The enamel-adhesive<br />

interface is markedly different and associated <strong>with</strong><br />

reduced bond strengths to resin composite, however<br />

in the majority of cases failure was cohesive <strong>with</strong>in<br />

the enamel 22 . Bacterial invasion of dentine tubules,<br />

and associated inflammatory change (secondary<br />

“Children <strong>with</strong> teeth affected by<br />

MIH undergo up to ten times the<br />

treatment of unaffected children<br />

by the age of 8 years and have<br />

significantly higher levels of dental<br />

anxiety and phobia”<br />

dentine formation), under apparently intact<br />

hypomineralised enamel has also been demonstrated<br />

using SEM techniques 23. Other investigations of<br />

the pulp status of MIH affected teeth have reported<br />

increased expression of an inflammatory mediator<br />

implicated in pain development, an increase in<br />

immune cells and increased innervation and<br />

vascularisation, providing a reason for the increased<br />

sensitivity and refractory nature <strong>with</strong> anaesthesia of<br />

these teeth 24,25.<br />

Management<br />

Unfortunately it is, as yet, impossible to use evidence<br />

based dentistry in the treatment of MIH as, while<br />

recommendations are supported theoretically by<br />

research evidence, only very limited clinical data<br />

is available. Generally it is advised clinicians utilize<br />

the apparently sound cervical enamel for bonding<br />

of ‘permanent’ restorations as marginal breakdown<br />

is otherwise commonly observed, however this<br />

strategy does involve the sacrifice of a great amount<br />

of enamel 26-28. Glass ionomer cements are often<br />

recommended, especially for early protection of<br />

the enamel, but currently there is no evidence<br />

beyond anecdotal for using this material either in<br />

vitro or in vivo 26, 27 . Despite this a recent <strong>Europe</strong>an<br />

Academy of Paediatric Dentistry policy document<br />

for MIH management included GIC restorations in its<br />

recommendations 29 .<br />

Also suggested was the use of preformed crowns<br />

which have been found to perform well and do not<br />

1: Hypomineralised tooth demonstrating both severe (post-eruptive breakdown on distal cusps) and mild (white<br />

demarcated opacity on mesio-buccal cusp tip) lesions. 2: Polished hypomineralised lesion demonstrating demarcated<br />

defect edge. 3: Polarised light image (water imbibition) demonstrating surface layer of improved physical properties in<br />

area of post-eruptive breakdown (blue layer). 4: Clinical images of hypomineralised teeth demonstrating demarcated<br />

opacities, post-eruptive breakdown and cavitation even before complete eruption.<br />

treatment plan<br />

11


vitro or in vivo 26, 27. Despite this a recent <strong>Europe</strong>an<br />

Academy of Paediatric Dentistry policy document<br />

for MIH management included GIC restorations in its<br />

recommendations 29 .<br />

Also suggested was the use of preformed crowns<br />

which have been found to perform well and do not<br />

need extensive tooth preparation thus conserving<br />

maximum tooth structure, and therefore options, for<br />

future treatments as these restorations cannot really<br />

be considered a permanent solution 29,30. Given the<br />

eventual outcome the restoration cycle, the rapidity<br />

<strong>with</strong> which MIH teeth can pass through this cycle<br />

and the costs associated <strong>with</strong> treatment (potentially<br />

endodontic treatment, fixed prosthodontics and<br />

eventual replacement <strong>with</strong> an implant at a relatively<br />

young age as other options are exhausted) it<br />

is recommended that extraction, ideally <strong>with</strong><br />

consultation and co-ordination <strong>with</strong> orthodontic<br />

advice, be considered for severely affected teeth.<br />

Acceptable outcomes, even <strong>with</strong>out (but preferably<br />

<strong>with</strong>) orthodontic intervention, can be achieved<br />

and cases should be assessed as to whether this<br />

option is more appropriate if extensive treatment<br />

seems otherwise inevitable 6,7,29 . It is commonly<br />

requested that extractions be delayed until the most<br />

orthodontically favourable time in which case interim<br />

restorations or preventive strategies may be needed<br />

in the interim. Preventive advice is based on the early<br />

caries/remineralisation model utilizing <strong>CPP</strong>-<strong>ACP</strong>,<br />

fluoride products and fissure sealants, however again<br />

the efficacy of such treatments is anecdotal only 29.<br />

References<br />

1. Weerheijm, K.L., B. Jalevik, and S. Alaluusua, Molar-incisor<br />

hypomineralisation. Caries Research, 2001. 35(5): p. 390-1.<br />

2. Weerheijm, K.L., et al., Prevalence of cheese molars in<br />

eleven-year-old Dutch children. Journal of Dentistry for<br />

Children, 2001. 68(4): p. 259-62.<br />

3. Crombie, F.A., et al., Molar incisor hypomineralization: a survey<br />

of members of the Australian and New Zealand Society<br />

of Paediatric Dentistry. Aust Dent J, 2008. 53(2): p. 160-6.<br />

4. Leppaniemi, A., P.L. Lukinmaa, and S. Alaluusua, Nonfluoride<br />

hypomineralizations in the permanent first molars<br />

and their impact on the treatment need. Caries Research,<br />

2001. 35(1): p. 36-40.<br />

5. Jalevik, B. and G.A. Klingberg, Dental treatment, dental fear<br />

and behaviour management problems in children <strong>with</strong><br />

severe enamel hypomineralization of their permanent first<br />

molars. International Journal of Paediatric Dentistry, 2002.<br />

12(1): p. 24-32.<br />

6. Williams, J.K. and A.J. Gowans, Hypomineralised first<br />

permanent molars and the orthodontist. <strong>Europe</strong>an Journal<br />

of Paediatric Dentistry, 2003. 4(3): p. 129-32.<br />

7. Mejare, I., E. Bergman, and M. Grindefjord, Hypomineralized<br />

molars and incisors of unknown origin: treatment outcome<br />

at age 18 years. International Journal of Paediatric<br />

Dentistry, 2005. 15(1): p. 20-8.<br />

8. Crabb, J.J. and W.P. Rock, Treatment planning in relation<br />

to the first permanent molar. British Dental Journal, 1971.<br />

131(9): p. 396-401.<br />

9. Jalevik, B., et al., The prevalence of demarcated opacities<br />

in permanent first molars in a group of Swedish children.<br />

Acta Odontologica Scandinavica, 2001. 59(5): p. 255-60.<br />

10. Jasulaityte, L., J.S. Veerkamp, and K.L. Weerheijm, Molar<br />

incisor hypomineralization: review and prevalence data<br />

from the study of primary school children in Kaunas/Lithuania.<br />

<strong>Europe</strong>an Archives of Paediatric Dentistry: Official<br />

Journal of the <strong>Europe</strong>an Academy of Paediatric Dentistry,<br />

2007. 8(2): p. 87-94.<br />

11. Jalevik, B., Prevalence and Diagnosis of Molar-Incisor-<br />

Hypomineralisation (MIH): A systematic review. Eur Arch<br />

Paediatr Dent. 11(2): p. 59-64.<br />

12. Weerheijm, K.L. and I. Mejare, Molar incisor hypomineralization:<br />

a questionnaire inventory of its occurrence in<br />

member countries of the <strong>Europe</strong>an Academy of Paediatric<br />

Dentistry (EAPD). International Journal of Paediatric Dentistry,<br />

2003. 13(6): p. 411-6.<br />

13. Crombie, F., D. Manton, and N. Kilpatrick, Aetiology of<br />

molar-incisor hypomineralization: a critical review. Int J<br />

Paediatr Dent, 2009. 19(2): p. 73-83.<br />

14. 57th Annual ORCA Congress July 7-10, 2010, Montpellier,<br />

France Abstracts. Caries Research. 44(3): p. 172-244.<br />

15. Mahoney, E., et al., Mechanical properties across hypomineralized/hypoplastic<br />

enamel of first permanent molar teeth.<br />

<strong>Europe</strong>an Journal of Oral Sciences, 2004. 112(6): p. 497-502.<br />

16. Fearne, J., P. Anderson, and G.R. Davis, 3D X-ray microscopic<br />

study of the extent of variations in enamel density in first<br />

permanent molars <strong>with</strong> idiopathic enamel hypomineralisation.<br />

British Dental Journal, 2004. 196(10): p. 634-8;<br />

discussion 625.<br />

17. Anonymous, 56th Congress of the <strong>Europe</strong>an-Organisation-for-Caries-Research<br />

(ORCA), Budapest, HUNGARY, July<br />

01 -04, 2009. Caries Research, 2009. 43(3): p. 179-241.<br />

18. Jalevik, B., et al., Secondary ion mass spectrometry and<br />

X-ray microanalysis of hypomineralized enamel in human<br />

permanent first molars. Archives of Oral Biology, 2001.<br />

46(3): p. 239-47.<br />

19. Mangum, J.E., et al., Surface integrity governs the<br />

proteome of hypomineralised enamel. Journal of Dental<br />

Research, Accepted for publication, April 2010.<br />

20. Mahoney, E.K., et al., Mechanical properties and microstructure<br />

of hypomineralised enamel of permanent teeth.<br />

Biomaterials, 2004. 25(20): p. 5091-100.<br />

21. Jalevik, B., W. Dietz, and J.G. Noren, Scanning electron<br />

micrograph analysis of hypomineralized enamel in<br />

Affected anterior teeth tend to present aesthetic<br />

problems only, rather than the breakdown, sensitivity<br />

and increased caries risk found when molars are<br />

involved. Management is therefore usually more<br />

straightforward and options include: microabrasion,<br />

bleaching and sealant and direct or eventually<br />

indirect restorations to improve the appearance 29.<br />

In conclusion, the apparent increasing prevalence<br />

of MIH creates the need for greater practitioner<br />

knowledge regarding the diagnosis of the condition<br />

and also the treatment options possible.<br />

About the authors<br />

Dr Felicity Crombie completed<br />

her BDSc <strong>with</strong> Honours at the<br />

University of Melbourne and works<br />

in private practice as well as teaching<br />

undergraduates. In 2007 Dr Crombie<br />

started her PhD studies investigating<br />

the properties of molars affected<br />

by enamel hypomineralisation and<br />

subsequently has published and presented on the<br />

topic of molar hypomineralisation<br />

locally and internationally.<br />

David John Manton [BDSc MDSc<br />

PhD FRACDS FICD] is the convener<br />

of Paediatric Dentistry at the<br />

Cooperative Centre for Oral Health<br />

Science, Melbourne Dental School,<br />

University of Melbourne.<br />

permanent first molars. International Journal of Paediatric<br />

Dentistry, 2005. 15(4): p. 233-240.<br />

22. William, V., et al., Microshear bond strength of resin<br />

composite to teeth affected by molar hypomineralization<br />

using 2 adhesive systems. Pediatric Dentistry, 2006. 28(3):<br />

p. 233-41.<br />

23. Fagrell, T.G., et al., Bacterial invasion of dentinal tubules<br />

beneath apparently intact but hypomineralized enamel<br />

in molar teeth <strong>with</strong> molar incisor hypomineralization.<br />

International Journal of Paediatric Dentistry, 2008. 18(5): p.<br />

333-340.<br />

24. Rodd, H.D., et al., Pulpal status of hypomineralized permanent<br />

molars. Pediatric Dentistry, 2007. 29(6): p. 514-20.<br />

25. Rodd, H.D., et al., Pulpal expression of TRPV1 in molar incisor<br />

hypomineralisation. <strong>Europe</strong>an Archives of Paediatric<br />

Dentistry: Official Journal of the <strong>Europe</strong>an Academy of<br />

Paediatric Dentistry, 2007. 8(4): p. 184-8.<br />

26. William, V., L.B. Messer, and M.F. Burrow, Molar incisor hypomineralization:<br />

review and recommendations for clinical<br />

management. Pediatric Dentistry, 2006. 28(3): p. 224-32.<br />

27. Mathu-Muju, K. and J.T. Wright, Diagnosis and treatment<br />

of molar incisor hypomineralization. Compendium of<br />

Continuing Education in Dentistry, 2006. 27(11): p. 604-10;<br />

quiz 611.<br />

28. Lygidakis, N.A., A. Chaliasou, and G. Siounas, Evaluation<br />

of composite restorations in hypomineralised permanent<br />

molars: a four year clinical study. <strong>Europe</strong>an Journal of<br />

Paediatric Dentistry, 2003. 4(3): p. 143-8.<br />

29. Lygidakis, N.A., et al., Best Clinical Practice Guidance for<br />

clinicians dealing <strong>with</strong> children presenting <strong>with</strong> Molar-<br />

Incisor-Hypomineralisation (MIH) An EAPD Policy Document.<br />

Eur Arch Paediatr Dent, 2010. 11(2): p. 75-82.<br />

30. Zagdwon, A.M., S.A. Fayle, and M.A. Pollard, A prospective<br />

clinical trial comparing preformed metal crowns and cast<br />

restorations for defective first permanent molars. <strong>Europe</strong>an<br />

Journal of Paediatric Dentistry, 2003. 4(3): p. 138-42.<br />

12 clinical corner<br />

mi.gceurope.com


White spot reversal protocol<br />

The following protocols were developed by clinicians in their own<br />

dental practices in the USA, and published by <strong>GC</strong> America.<br />

Steps to white spot reversal<br />

• Take photos of the white spot lesion prior to the<br />

start.<br />

• It is important during microabrasion for the<br />

clinician not to over abrade the tooth surface,<br />

careful attention needs to be paid to the etching<br />

materials, their concentrations and application<br />

time.<br />

• Apply 37% phosphoric acid gel to white spot<br />

lesions, (10/15 sec. To 2 min. – suggested to be<br />

conservative), Rinse.<br />

• Gently pumice for 10 - 20 sec., (<strong>with</strong> non<br />

fluoridated, non glycerine pumice - suggest flour of<br />

pumice), Rinse.<br />

• Review the effect sometimes may have to etch a<br />

second time.<br />

• Some dentists prefer to pumice first, then etch.<br />

• Apply thick layer of MI Paste to the etched teeth for<br />

5 minutes.<br />

• Instruct patient to use MI Paste 2X daily for 5<br />

minutes.<br />

• Custom tray is optional.<br />

• Have patient return for evaluation in 7 -10 days.<br />

• Repeat procedure if necessary.<br />

Successful cases<br />

Clinician: Dr Scott Munro - Racine, WI, USA<br />

Before<br />

After<br />

Treatment protocol followed:<br />

09/18/07 3 Minute Etch, 5 Minute MI Paste Treatment<br />

09/24/07 3 Minute Etch, 5 Minute MI Paste Treatment<br />

10/04/07 3 Minute Etch, 5 Minute MI Paste Treatment<br />

10/15/07 3 Minute Etch, 5 Minute MI Paste Treatment<br />

- Bleach 15% Opalescence<br />

10/18/07 3 Minute Etch, 5 Minute MI Paste Treatment-<br />

Bleach 15% Opalescence<br />

11/01/07 3 Minute Etch, 5 Minute MI Paste Treatment<br />

11/29/07 3 Minute Etch, 5 Minute MI Paste Treatment<br />

Notes<br />

• No restorative work was done on patient<br />

• MI Paste was used and some light microabrasion<br />

was done on cusp tips. #9 wasn’t bleached<br />

internally, but was whitened <strong>with</strong> ZOOM in office.<br />

Patient wore trays for 5 minutes, twice daily.<br />

clinical corner<br />

13


Clinician: Dr Stephanie Benton - Grand Rapids, MI, USA<br />

Before<br />

Treatment protocol followed:<br />

• Teeth were etched twice, for 20 second intervals.<br />

• No pumice was used.<br />

• MI Paste was placed immediately on teeth following etching and wore trays at night time only.<br />

• Immediate results were seen over the first weekend.<br />

• Patient continued to wear the trays for 2-3 weeks at night time.<br />

Clinician: Dr Brett Kessler - Denver, CO, USA<br />

Before<br />

Before close-up<br />

Treatment protocol followed:<br />

• Etched # 8 & 9 for 3 minutes<br />

• Gave MI Paste <strong>with</strong> trays to 15 minutes before bed,<br />

after 3 days<br />

• Patient used MI Paste for the spots were gone.<br />

14<br />

clinical corner<br />

After<br />

After<br />

After close-up<br />

• The after photos are 2 weeks after the one time<br />

etching and daily use.<br />

• The patient used approximately 1/2 of the tube of<br />

MI Paste to achieve these results.<br />

mi.gceurope.com


Clinician: Dr Ivan A. Serdar - San Francisco, CA, USA<br />

Before<br />

After<br />

Treatment protocol followed:<br />

12/02/08 - Pumice, rinse, 1 minute etch <strong>with</strong> 37%<br />

Phosphoric acid, rinse, blot, 5 minutes MI Paste.<br />

01/07/09 - Pumice, rinse, 1 minute etch <strong>with</strong> 37%<br />

Phosphoric acid, rinse, blot, 5 minutes MI Paste.<br />

01/26/09 - Pumice, rinse, minute etch <strong>with</strong><br />

Phosphoric acid, rinse, blot, minutes Paste.<br />

02/25/09 - Pumice, rinse, 1 minute etch <strong>with</strong> 37%<br />

Phosphoric acid, rinse, blot, 5 minutes MI Paste.<br />

04/01/09 - Pumice, rinse, 1 minute etch <strong>with</strong> 37%<br />

Phosphoric acid, rinse, blot, 5 minutes MI Paste.<br />

04/29/09 - Pumice, rinse, 1 minute etch <strong>with</strong> 37%<br />

Phosphoric acid, rinse, blot, 5 minutes MI Paste.<br />

Notes<br />

Patient used trays at home for the duration of this<br />

treatment and placed MI Paste in her trays for 5<br />

minutes, twice a day. Patient also used regular<br />

strength Whitestrips at home for three weeks.<br />

Clinician: Dr Rubin and Dr Pong - Cincinnati, OH, USA<br />

Before<br />

After<br />

Treatment protocol followed:<br />

• 2 Minute etch <strong>with</strong> 37% phosphoric acid (blue gel)<br />

• Heavy pumice<br />

• Dispense tube of MI Paste or MI Paste Plus. Patient<br />

apply/rub<br />

• MI Paste <strong>with</strong> finger to affected areas for 10<br />

seconds, daily at bedtime. Re-evaluate in 2 weeks<br />

• Repeat sequence as needed for desired result.<br />

• Treatment was over the course of 1 month<br />

9/3/2008-9/29/2008.<br />

clinical corner<br />

15


Topical <strong>CPP</strong>-<strong>ACP</strong> crème (Tooth Mousse):<br />

more evidence that demands a verdict<br />

By Laurence J Walsh<br />

Casein Phosphopeptide-Amorphous Calcium<br />

Phosphate (<strong>CPP</strong>-<strong>ACP</strong>) is a unique naturally derived<br />

protein-based remineralizing technology which is now<br />

used globally in chewing gums and topical crèmes.<br />

The unique phosphopeptides are derived from milk<br />

caseins, and are complexed <strong>with</strong> amorphous calcium<br />

phosphate, to form stable complexes which are<br />

nanoparticles of some 2 nm in diameter <strong>with</strong> a large<br />

surface area for mineral exchange Cross et al. 2006).<br />

The configuration of the <strong>ACP</strong> in the <strong>CPP</strong>-<strong>ACP</strong> complex<br />

differs completely from that found in macromolecular<br />

aggregates of <strong>ACP</strong>, as has been included in some<br />

current prophylaxis pastes and bleaching gels.<br />

<strong>CPP</strong>-<strong>ACP</strong> nanocomplexes act as biological<br />

calcium phosphate delivery vehicles, and are<br />

able to boost levels of bio-available calcium and<br />

phosphate in saliva and plaque fluid <strong>with</strong>out causing<br />

indiscriminate precipitation of calcium salts. This<br />

makes this material particularly effective in the<br />

remineralization of early enamel lesions, and in the<br />

treatment of other types of enamel opacities. The<br />

efficacy of these nanocomplexes as anti-cariogenic<br />

agents has been demonstrated in numerous animal<br />

and in situ human caries studies (Reynolds 1997,<br />

1998, 2008, 2009; Cross et al. 2007), as well as in<br />

clinical trials. Over the past decade, the use of<br />

products containing <strong>CPP</strong>-<strong>ACP</strong> nanocomplexes has<br />

become a well established part of clinical practice<br />

across the globe. The clinical use of this technology<br />

is supported by a large body of refereed papers and<br />

conference presentations as well as by systematic<br />

reviews, the highest form of evidence in the<br />

pyramid of evidence-base practice. For example, a<br />

2006 systematic review focused on chewing gums<br />

and lozenges enriched <strong>with</strong> <strong>CPP</strong>-<strong>ACP</strong> (Yengopal &<br />

Mickenautsch, 2006 & 2009), identified over 120<br />

journal articles on <strong>CPP</strong>-<strong>ACP</strong> technology, which<br />

included laboratory trials and animal studies as well<br />

as clinical trials and numerous in situ clinical studies.<br />

In Australia and in many other parts of the world,<br />

the most commonly used <strong>CPP</strong>-<strong>ACP</strong> product is the<br />

topical crème which contains 10% <strong>CPP</strong>-<strong>ACP</strong>. This<br />

product, which is known alternatively as Tooth<br />

Mousse or MI Paste, is intended for both in-office<br />

and at-home use. The purpose of this article is<br />

to summarize the global research effort which<br />

underpins the current clinical applications of Tooth<br />

Mousse (TM) and its related fluoride-containing<br />

counterpart, Tooth Mousse Plus (TMP). The article<br />

draws on the refereed literature, including both<br />

journal papers and presentations at international and<br />

regional meetings of the International Association for<br />

Dental Research (IADR), the peak international body<br />

for dental research, over the period from January<br />

2002 to August 2010.<br />

Bio-availability of calcium and phosphate ions<br />

In most preventive protocols, TM is applied daily in a<br />

pea-size amount using a finger to the labial surfaces<br />

of the teeth immediately before bed. By dissolving<br />

slowly, the material contributes bio-available calcium<br />

and phosphates to the saliva, and is able to promote<br />

remineralization at a time when salivary defenses are<br />

at their lowest point. TM can be used in patients of all<br />

ages as the material is classified as safe to ingest.<br />

The release of ions from TM has been examined in<br />

considerable detail. The release of ions at neutral pH<br />

was reported by Paterson et al. (2008) who dissolved<br />

TM directly into deionized water and then used a<br />

calcium ion-selective electrode to measure calcium<br />

ion release. The free calcium ion concentration in<br />

the solution increased <strong>with</strong> time in a saturating<br />

exponential manner, <strong>with</strong> approximately 95 % release<br />

after only 15 minutes. This rapid release means that<br />

when the crème is applied to tooth surfaces there<br />

will be a rapid increase in calcium ion concentration<br />

in the plaque fluid and saliva. Their supersaturation<br />

for calcium <strong>with</strong> respect to tooth enamel drives<br />

remineralization and prevents mineral loss.<br />

Comparative studies <strong>with</strong> a broad range<br />

of toothpastes, gels, liquids claimed to have<br />

remineralizing or desensitizing actions (including<br />

NovaMin ®, ClinPro ® Tooth Creme, Clin Pro 5000,<br />

and ReminPro ®) reveal that calcium contained in<br />

these products has low water solubility and poor<br />

bio-availability, unlike the situation for TM and TMP.<br />

The level of water soluble calcium per gram of crème<br />

in TM or TMP (321.8 ± 2.6 µmol/g) is some 14 times<br />

or greater than any of these other products (Cai et<br />

al. 2009; Yasuda et al. 2010). Tooth Mousse Plus also<br />

has been shown to contain the highest amount of<br />

water soluble phosphate (245.7 ± 2.7 µmol/g) of any<br />

currently available products. The rapid release of<br />

calcium ions (<strong>with</strong>in 1 hour) has been confirmed in<br />

other studies of TM, including those conducted by<br />

commercial competitors (Burwell et al. 2009).<br />

The high water solubility and bioavailability of the<br />

calcium, phosphate and fluoride in TM and TMP is<br />

due to this being a protein technology (containing<br />

casein phosphopeptides), whereas all other marketed<br />

16 Clinical corner<br />

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Table 1. Prevention and treatment of enamel caries using Tooth Mousse in laboratory models<br />

Author Year Location Design Outcomes<br />

products are inorganic in nature and lack the ability<br />

to stabilize the calcium and phosphate ions.<br />

Prevention of mineral loss in caries models<br />

Topical application of TM immediately before a<br />

cariogenic challenge has been shown to prevent<br />

Enamel caries<br />

Sato 2003 Tokyo Enamel slabs <strong>with</strong> demin gel TM buffered acids produced<br />

(microhardness) by S. mutans<br />

TM reduced enamel demin from<br />

acidic gel and S. mutans fermentation.<br />

Takamizawa 2005 Tokyo Enamel slabs <strong>with</strong> demin gel TM preserved the inorganic component<br />

(ultrasound) of enamel by preventing demin.<br />

Sakaguchi 2005 Tokyo Enamel slabs <strong>with</strong> demin gel TM preserved the inorganic component<br />

(QLF) of enamel by preventing demin.<br />

Sudjalimi 2006 Melbourne Extracted teeth in demin gel TM reduced mineral loss around<br />

(QLF) orthodontic brackets.<br />

Manton 2007 Melbourne Enamel slabs <strong>with</strong> white TM caused more remin of white spot<br />

spot lesions lesions than human saliva.<br />

Lovel 2007 Liverpool Enamel slabs <strong>with</strong> white TM was more effective than 1000 ppm<br />

spot lesions (QLF) F toothpaste in promoting remin of WSL<br />

Kim 2007 South Korea Enamel slabs <strong>with</strong> WSL TM was more effective than 3000 ppm<br />

(microhardness) F solution in preventing demin.<br />

Kumar 2008 Hong Kong Enamel slabs <strong>with</strong> WSL TM remineralized WSL and showed a<br />

higher remineralizing potential when<br />

applied after the use of a fluoride<br />

toothpaste.<br />

Adebayo 2008 Melbourne Enamel slabs TM treatment of intact enamel<br />

improves resistance to phosphoric<br />

acid etching<br />

Kao 2008 West Virginia Enamel slabs TM treatment increases acid resistance<br />

of enamel when exposed to a demin gel.<br />

Setien 2008 Dallas Enamel slabs <strong>with</strong> WSL TM treatment increased the<br />

(microhardness) microhardness of demineralized enamel.<br />

Theerapiboon 2008 Bangkok Enamel slabs <strong>with</strong> WSL (PLM) TM treatment reduced lesion volume<br />

and caused remin in WSL in both<br />

permanent and deciduous enamel.<br />

Huang 2008 Minneapolis Enamel slabs eroded TM treatment improved enamel<br />

<strong>with</strong> Coke® hardness more than artificial saliva.<br />

Kallayahi 2008 Bangkok Enamel slabs TM treatment protected enamel from<br />

(microhardness) softening from cola drink exposure.<br />

Behnan 2009 Ann Arbor Enamel slabs TM prevented enamel demineralization<br />

(QLF) around orthodontic brackets during<br />

an in-vitro acid challenge.<br />

Elsayad 2009 Cairo Molar teeth <strong>with</strong> demin TM caused remin, which was enhanced<br />

when F was added simultaneously.<br />

Chapman 2010 Bristol Enamel slabs (profilometry) TMP and TMP reduced enamel surface<br />

loss from citric acid challenge.<br />

F = fluoride, QLF = Quantitative light fluorescence; PLM = polarizing light microscopy, WSL = white spot lesions.<br />

demineralization of enamel during subsequent<br />

challenge, and also to reduce the pH reduction<br />

caused by S. mutans fermentation (Sato et al. 2003).<br />

This capacity to buffer acids produced by cariogenic<br />

bacteria adds to other ecological effects of TM on<br />

dental plaque. TM has benefits in preventing root<br />

clinical corner<br />

17


surface caries as well as enamel caries (Tables 1-3).<br />

Numerous laboratory studies have documented that<br />

TM is more effective than saliva for remineralization<br />

after caries- and erosion-like assaults to the enamel<br />

(Table 1). This holds true regardless of the methods<br />

which are used to assess the integrity of the<br />

enamel. Preventive benefits of TM and TMP are now<br />

recognized to extend to root surfaces as well as<br />

enamel (Table 2), and evidence of arrest and reversal<br />

of root surface caries has also been presented (Vlacic<br />

et al. 2007).<br />

As well as effects mediated through promoting<br />

remineralization and inhibiting demineralization, it is<br />

now recognized that TM can exert ecological effects<br />

on the dental plaque biofilm. A recent large scale<br />

clinical trial reported that daily use of TM in infants<br />

from the time of first tooth eruption had similar<br />

effects on plaque acid production as daily use of<br />

0.12% chlorhexidine gel (Plonka et al. 2010).<br />

Visible reversal of white spot carious lesions<br />

Early case reports of visible reversal of enamel white<br />

spot lesions (WSL) in young adult patients in Australia<br />

Table 2. Other Laboratory Studies of Tooth Mousse<br />

(Walsh 2004; Walsh 2007) and later in Japan (from 2002)<br />

(Reynolds & Walsh, 2005), <strong>Europe</strong> (Ardu et al. 2007) and<br />

North America (Milnar, 2007) have been followed by in<br />

situ studies of laboratory-created WSL (Manton et al.<br />

2007) and full scale randomized controlled clinical trials<br />

in patients <strong>with</strong> naturally occurring WSL (Andersson<br />

et al. 2006; Kitasako et al. 2009; Bailey et al. 2009; Zhou<br />

et al. 2009; Yazicioglu et al. 2010). Cases of reversal of<br />

moderate fluorosis have also been presented (Walsh<br />

2003; Walsh 2004; Reynolds & Walsh 2005; Walsh 2007;<br />

Ng & Manton 2007).<br />

Recent reviews have concluded that predictable<br />

remineralization of enamel white spot lesions<br />

(WSL) can be achieved clinically by using frequent<br />

applications of TM as a self-administered topical<br />

therapy (Ilena et al. 2009; Reynolds 2009). This<br />

significant body of work (summarized in Table 3)<br />

demonstrates that dramatic cosmetic changes occur<br />

in enamel as WSL undergo reversal during treatment<br />

<strong>with</strong> TM on a daily basis. A particular risk group where<br />

TM is useful for gaining regression of white spot<br />

lesions is patients who are undergoing orthodontic<br />

treatment (Table 4).<br />

Author Year Location Design Outcomes<br />

Root caries<br />

Hicks 2005 Houston Root segments <strong>with</strong> demin gel TM enhanced the resistance of root<br />

(PLM) surfaces to artificial caries formation,<br />

when compared <strong>with</strong> fluoride rinse<br />

(0.05% NaF).<br />

Rahiotis 2007 Athens Dentine slabs <strong>with</strong> demin gel TM treatment reduced demin and<br />

enhanced remin of dentine.<br />

Xie 2007 Chicago Root segments <strong>with</strong> demin gel TM treatment increased the hardness<br />

(microhardness) of dentine.<br />

Trajtenberg 2007 Houston Root segments <strong>with</strong> demin gel TM treatment improved caries<br />

(PLM) resistance of root surfaces.<br />

Garcia-Godoyi 2009 Fort Lauderdale Root segments <strong>with</strong> demin gel TM and TMP protected root surfaces<br />

(PLM) from an artificial caries challenge.<br />

Other applications<br />

Wong 2010 Melbourne Teeth undergoing bleaching A 2 week application of TM prior to<br />

the use of an in-office bleaching gel did<br />

not adversely affect the bleaching<br />

effectiveness, but reduced the levels of<br />

hydrogen peroxide entering the pulp<br />

chamber.<br />

Augustson 2010 Minneapolis Enamel eroded <strong>with</strong> HCl After HCL erosion, 60 minutes exposure<br />

(microhardness) to TMP or TM (but not 3000 ppm F rinse)<br />

increased the enamel hardness. Greater<br />

recovery seen <strong>with</strong> TMP than <strong>with</strong> TM.<br />

Gomes 2010 San Paulo De-proteinated enamel TM applied after in-office bleaching<br />

helped to restore the glossy nature of<br />

the enamel surface.<br />

18 Clinical corner<br />

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Table 3. Selected clinical studies of <strong>CPP</strong>-<strong>ACP</strong> products<br />

Author Year Location Design Outcomes<br />

While it is now well established that TM can cause<br />

reversal of WSL, it is remarkable that there are as<br />

yet no clinical trials or case reports in the literature<br />

showing visual reversal of enamel WSL for other<br />

agents such as NovaMin or ClinPro Tooth Crème<br />

which claim to have remineralizing actions.<br />

TMP is a potent agent for promoting regression and<br />

reversal of WSL. Mixtures of <strong>CPP</strong>-<strong>ACP</strong> <strong>with</strong> fluoride<br />

(TMP) and <strong>CPP</strong>-ACFP solutions have been shown<br />

to remineralize enamel subsurface lesions in vitro<br />

by depositing fluorapatite. This remineralization is<br />

accompanied by improved translucency and reduced<br />

opacity of the white spot lesions, as reversal occurs<br />

and mineral content increases (Cochrane et al. 2006).<br />

Chewing Gums<br />

Cai 2003 Melbourne RCT, in situ model, N=10, Incorporation of <strong>CPP</strong>-<strong>ACP</strong> into a lozenge<br />

over 14 days increased enamel subsurface lesion<br />

remineralization relative to a control<br />

sugar-free lozenge.<br />

Manton 2005 Melbourne RCT, in situ model, N=10, <strong>CPP</strong>-<strong>ACP</strong> gum produced 75-107% more<br />

over 14 days remineralization than sugar-free gums.<br />

Cai 2006 Melbourne RCT, in situ model, N=10, <strong>CPP</strong>-<strong>ACP</strong> gum produced more<br />

over 14 days remineralization than chewing <strong>with</strong><br />

placebo gum. Extended acid challenge<br />

of the remineralized lesions showed that<br />

the mineral formed was more acid<br />

resistant.<br />

Iijima 2006 Nagasaki RCT, in situ model, N=20, <strong>CPP</strong>-<strong>ACP</strong> gum produced remin of<br />

over 14 days subsurface enamel <strong>with</strong> mineral of<br />

higher crystallinity and greater acid<br />

resistance than when remin occurs <strong>with</strong><br />

saliva.<br />

Morgan 2008B Melbourne RCT, N=2720 children, <strong>CPP</strong>-<strong>ACP</strong> sugar-free gum slowed<br />

over 2 years progression and enhanced regression of<br />

approximal caries relative to a control<br />

sugar-free gum.<br />

Toothpaste<br />

Reynolds 2006 Melbourne RCT, in situ model, N=10, Toothpaste <strong>with</strong> 2% <strong>CPP</strong>-<strong>ACP</strong> produced<br />

over 14 days remin similar to 2800 ppm F toothpaste.<br />

Rao 2009 Manipal RCT, N=150 children, Toothpaste <strong>with</strong> 2% <strong>CPP</strong> caused a<br />

over 2 years significant reduction in caries increment<br />

versus placebo, and was equally as<br />

effective as a toothpaste containing<br />

1190 ppm F.<br />

Mouthrinse<br />

Shen 2006 Melbourne RCT, in situ model, N=10, Mouthrinse containing 0.5% <strong>CPP</strong>-<strong>ACP</strong><br />

over 10 days at pH 5.5 produced greater remin of<br />

enamel subsurface lesions than the<br />

same rinse at pH of 7.0.<br />

RCT = randomized controlled clinical trial.<br />

Treatment of cervical dentinal hypersensitivity (CDH)<br />

There is a significant literature regarding the strong<br />

interactions which occur between TM and dentine<br />

(Adebayo et al. 2008 A&B, 2009, 2010). One of the first<br />

clinical trials using TM to treat CDH was undertaken<br />

in Belgium in 2004. The study involved 11 private<br />

practitioners, whose patients <strong>with</strong> CDH were instructed<br />

to apply TM for 21 days, immediately after the evening<br />

brushing, leaving the material for 3 minutes, and<br />

spreading it across the mouth, and then leaving it<br />

in place during sleep. The patient cohort reported a<br />

reduction in sensitivity, particularly to stimulation <strong>with</strong><br />

air as opposed to tactile stimuli. Daily diaries which<br />

recorded symptoms of CDH showed a progressive<br />

clinical corner<br />

19


eduction from the first day of treatment over the<br />

following 3 weeks. Half of the treated patients reported<br />

that the general reduction in CDH symptoms was<br />

sufficiently great that they wished to repeat the<br />

treatment if symptoms of sensitivity recurred (Poitevin<br />

et al. 2004). A later series of randomized controlled<br />

clinical trials conducted in Brisbane showed that TM<br />

reduced sensitivity to air, osmotic, thermal and tactile<br />

stimuli, <strong>with</strong> equal effectiveness to potassium nitrate<br />

toothpaste (Walsh et al. 2006; Vlacic 2007, Walsh 2010).<br />

This finding has been confirmed by more recent studies<br />

(Duan et al. 2009). This aligns <strong>with</strong> studies which show<br />

that a single application of TM can coat and partially<br />

occlude dentine tubules, and resist thermocycling<br />

(Hiller et al. 2008), but is insufficient to give permanent<br />

resolution of sensitivity symptoms (Table 5).<br />

Tooth Mousse Plus<br />

<strong>CPP</strong> is able to stabilize amorphous calcium fluoride<br />

phosphate (<strong>CPP</strong>-ACFP), which allows additive effects<br />

on remineralization compared <strong>with</strong> the fluoride or<br />

Table 4. Clinical trials showing reversal of WSL by Tooth Mousse<br />

<strong>CPP</strong>-<strong>ACP</strong> alone (Cochrane et al. 2006; Sakaguchi<br />

et al. 2006). Moreover, <strong>CPP</strong>-<strong>ACP</strong> promotes the<br />

incorporation of fluoride into plaque and sub-surface<br />

enamel, producing effects superior to those which<br />

can be achieved using fluoride alone (Reynolds<br />

et al. 2006) (Table 5). Early studies showed that<br />

addition of 900 ppm fluoride to TM increased the<br />

acid resistance of the product formed when enamel<br />

lesions were remineralized, compared <strong>with</strong> using<br />

TM alone (Kariya et al. 2004). This level of fluoride<br />

was designed to provide the correct ionic ratio of<br />

components for remineralization. The inclusion of<br />

fluoride in TM to create TMP has been shown to<br />

enhance the resistance of enamel surfaces to in vitro<br />

caries formation, compared <strong>with</strong> TM or fluoride alone<br />

(Hicks 2006). A range of studies support the greater<br />

potential of TMP as a treatment agent over and above<br />

TM (Table 6).<br />

Direct comparisons of TMP <strong>with</strong> TM show the<br />

superior remineralizing capabilities of Tooth Mousse<br />

Plus, however, because of its fluoride content (900<br />

Author Year Location Design Outcomes<br />

Reversal of white spot lesions<br />

Manton 2006 Melbourne RCT, in situ model, N=6, TM produced 551% more remin of<br />

over 10 days enamel WSL than the placebo crème.<br />

Sakaguchi 2006 Tokyo In situ study, N=5 subjects, TM gave greater remin than 950 ppm<br />

7 days fluoride toothpaste, and even greater<br />

remin occurred <strong>with</strong> TMP, indicating<br />

synergy of fluoride <strong>with</strong> <strong>CPP</strong>-<strong>ACP</strong>.<br />

Vlacic 2007 Brisbane RCT, N=16, over 12 months TM in patients <strong>with</strong> salivary dysfunction<br />

arrested cervical lesions, and improved<br />

the stimulated salivary flow rate and pH<br />

over time.<br />

Andresson 2007 Halmstad Cohort study, N=26, TM caused a reduction in post-<br />

over 12 months orthodontic WSL over time, and was<br />

better than F mouthwash combined<br />

<strong>with</strong> F toothpaste.<br />

Morgan 2008A Melbourne RCT, N=45 subjects, 12 weeks TM produced more regression of WSL<br />

remaining after orthodontics than the<br />

placebo control at 12 weeks.<br />

Kitasako 2009 Tokyo Cohort study, N=7 subjects, TM produced remineralization of WSL<br />

6 months over 6 months, and increased the surface<br />

pH of the lesions (using a micro sensor).<br />

Zhou 2009 Changchun Cohort study, N=10 subjects, TMP reduced visible enamel<br />

2 months demineralization and improved the<br />

appearance of long-standing post-<br />

orthodontic WSL.<br />

Reynolds 2010 Melbourne RCT, in situ model, N=6, TM and TMP (but not ClinPro) increased<br />

over 10 days salivary calcium and phosphate levels,<br />

and caused remin of enamel WSL.<br />

Yazicioglu 2010 Istanbul Cohort study, N=26, TMP caused remineralization of WSL on<br />

over 28 days both smooth and occlusal surfaces.<br />

20 Clinical corner<br />

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ppm), TMP is not suitable for use in children aged<br />

less than 7 years, because of concerns regarding<br />

ingestion of fluoride.<br />

<strong>CPP</strong>-<strong>ACP</strong> inclusion in chewing gums<br />

The inclusion of <strong>CPP</strong>-<strong>ACP</strong> in chewing gums (such as<br />

Recaldent ) is a well established caries preventive<br />

measure (Table 3). Early studies of this approach used<br />

in situ studies (Cai et al. 2003) and then progressed<br />

to randomized, double blind cross-over designs to<br />

compare <strong>CPP</strong>-<strong>ACP</strong> containing gums <strong>with</strong> several<br />

commercial sugar-free gums. Subjects in these<br />

studies chewed the various gums for a 20 minute<br />

period 4 times per day for 14 days. By using paired<br />

Table 5. Selected clinical studies of Tooth Mousse<br />

enamel half slabs, precise determinations of mineral<br />

levels could be made. These studies showed that <strong>CPP</strong>-<br />

<strong>ACP</strong> gum produced 75-107% more remineralization<br />

than sugar-free gums (Manton 2005). It is well known<br />

that xylitol-based gums reduces the caries increment,<br />

but have little or no effect on approximal caries<br />

(Antonio et al. 2009). In contrast, gums containing<br />

<strong>CPP</strong>-<strong>ACP</strong> are highly effective at remineralizing<br />

WSL, and have been shown to arrest and reverse<br />

approximal lesions in a large scale clinical trial<br />

(Morgan et al. 2008 A & B).<br />

Recaldent gum is ideally suited to both child and<br />

adult patients where a lifestyle activity is linked to<br />

sub-clinical dehydration, and the patient suffers the<br />

Author Year Location Design Outcomes<br />

Cervical dentinal hypersenitivity<br />

Poitevin 2004 Leuvin Cohort study, N=61 subjects, TM reduced sensitivity air and tactile<br />

over 21 days stimuli.<br />

Kowalczyk 2006 Poland Cohort study, N=13 subjects, A single application of TM gave<br />

over 4 weeks immediate benefit on response to air<br />

stimulation. There was no further<br />

treatment so relapse occurred.<br />

Walsh 2006 Brisbane RCT, N=36 subjects, TM reduced sensitivity to air, osmotic,<br />

over 56 days, versus thermal and tactile stimuli, <strong>with</strong> equal<br />

potassium nitrate toothpaste effectiveness to potassium nitrate<br />

toothpaste.<br />

Vlacic 2007 Brisbane RCT, N=12, over 12 months TM caused a progressive reduction in<br />

sensitivity to air stimulation, and also<br />

improved stimulated salivary flow and pH.<br />

Duan 2009 Wuhan RCT, N=30 subjects, 14 days TM reduced sensitivity <strong>with</strong> equal<br />

effectiveness to potassium nitrate gel.<br />

Other applications<br />

Aytepe 2008 Istanbul Cohort study, N=15 children, TM elevated saliva buffering capacity<br />

56 days and plaque pH over 8 weeks in children<br />

<strong>with</strong> cerebral palsy.<br />

Caruana 2009 London RCT, N=15 subjects TM applied immediately before a sucrose<br />

challenge reduced plaque acid<br />

production.<br />

Rahiotis 2009 Athens Cohort study, N=6 subjects, A single application of TM forms a<br />

8 hours. surface coating which attaches to metal<br />

surfaces, making these smoother. These<br />

surface films retain calcium phosphates.<br />

Amornpipithkul 2009 Bangkok Cohort study, N=21 children, Daily application of TM increased plaque<br />

14 days calcium and inorganic phosphate levels<br />

in a time-dependent manner.<br />

Baroni 2010 Bologna Cohort study, n=30 children, TM improved the morphology and<br />

3 years microstructure of the enamel in teeth<br />

affected by molar incisor hypoplasia.<br />

Plonka 2010 Brisbane RCT, N=345 infants, 2 years TM suppressed the emergence of S.<br />

mutans in the oral microflora, and<br />

lowered dental plaque acid production.<br />

clinical corner<br />

21


problems from depressed salivary pH and flow under<br />

resting conditions. Because gum can be incorporated<br />

into a range of outdoor and exerting activities, the<br />

introduction of Recaldent gum should be considered<br />

for patients who undertake strenuous activity, for<br />

example, through outdoor exercise, outdoor work, or<br />

Table 6. Studies of <strong>CPP</strong>-<strong>ACP</strong> <strong>with</strong> fluoride (Tooth Mousse Plus)<br />

gym training sessions. The timing is important since<br />

the stimulation of salivary flow achieved by the gum<br />

will occur at a time when otherwise resting flow and<br />

pH would be depressed. Recaldent gum provides an<br />

excellent preventive effect, and is easily incorporated<br />

into a busy modern lifestyle.<br />

Author Year Location Design Outcomes<br />

Kariya 2004 Tokyo In vitro, enamel slabs <strong>with</strong> TMP reduced enamel mineral loss<br />

demin gel compared <strong>with</strong> TM. Acid resistance of<br />

remineralized lesions was greater for<br />

TMP compared <strong>with</strong> TM.<br />

Hicks 2006 Houston In vitro, enamel slabs <strong>with</strong> TMP enhanced the resistance of enamel<br />

demin gel surfaces to in vitro caries formation<br />

compared <strong>with</strong> TM or fluoride alone.<br />

Itthagarun 2006 Gold Coast In vitro, enamel slabs <strong>with</strong> TM remineralized initial enamel lesions,<br />

demin gel and gave more remineralization when<br />

applied as a topical coating after the use<br />

of fluoride toothpaste.<br />

Sudjalimi 2006 Melbourne In vitro, extracted teeth in TMP was better at reduced mineral loss<br />

demin gel (QLF) around orthodontic brackets than TM<br />

or fluoride alone.<br />

Reynolds 2006 Melbourne RCT, in situ model, N=10, Toothpaste containing 2% <strong>CPP</strong>-<strong>ACP</strong><br />

over 14 days plus 1100 ppm F was superior to paste<br />

<strong>with</strong> <strong>CPP</strong>-<strong>ACP</strong> alone and to 2800 ppm F<br />

toothpaste. Remineralized lesions were<br />

relatively acid resistant.<br />

Reynolds 2006 Melbourne RCT, N=10, over 14 days Mouthrinses containing 2% <strong>CPP</strong>-<strong>ACP</strong><br />

plus 450 ppm F increased the<br />

incorporation of fluoride ions into plaque<br />

to achieve over double that obtained<br />

<strong>with</strong> 450 ppm F rinse alone.<br />

Sakaguchi 2006 Tokyo In situ study, N=5 subjects, TMP gave greater remin than either TM<br />

7 days or 950 ppm fluoride toothpaste.<br />

Kim 2007 Sth Korea In vitro, enamel slabs <strong>with</strong> TMP was more effective than TM alone<br />

WSL (microhardness) or 3000 ppm F solution in preventing<br />

demin.<br />

Turssi 2008 San Paulo In vitro, enamel slabs <strong>with</strong> Treatment of eroded enamel <strong>with</strong> TMP<br />

erosion lesions (microhardness) reduced progression of erosion<br />

compared <strong>with</strong> the untreated control.<br />

Cochrane 2008 Melbourne In vitro, enamel slabs <strong>with</strong> WSL <strong>CPP</strong>-<strong>ACP</strong> and <strong>CPP</strong>-ACFP solutions<br />

promoted high levels of remineralization<br />

throughout the body of enamel WSL.<br />

Hamba 2010 Tokyo In vitro, enamel slabs <strong>with</strong> TMP prevented demineralization more<br />

demin gel (micro CT) effectively than TM <strong>with</strong>out F, and F alone.<br />

Hicks 2010 Houston In vitro, enamel slabs <strong>with</strong> TMP reduced lesion depths as effectively<br />

demin gel (PLM) as a 5000 ppm F toothpaste despite<br />

having a fluoride content of only 900<br />

ppm F.<br />

Cochrane 2010 Melbourne In vitro, enamel slabs <strong>with</strong> TMP produced high percentages of<br />

WSL and orthodontic brackets remineralization of WSL, which reduced<br />

the extent of enamel damage caused by<br />

bracket removal subsequently.<br />

RCT = randomized controlled clinical trial.<br />

22 Clinical corner<br />

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Extending the range of clinical applications<br />

The addition of <strong>CPP</strong>-<strong>ACP</strong> to existing foods has<br />

been shown to enhance their dental health<br />

benefits. Addition of <strong>CPP</strong>-<strong>ACP</strong> to cheese and milk<br />

at concentrations from 0.2-0.5% has been shown<br />

in laboratory studies to reduce mineral loss in<br />

enamel cased by acid exposure, and to enhance<br />

remineralization (Minami et al. 2004; Walker et al.<br />

2009).<br />

Likewise, TM has been shown to increase the<br />

hardness of enamel which has been eroded by<br />

repeated contact <strong>with</strong> acidic drinks such as colas,<br />

improving mineral uptake beyond that possible<br />

<strong>with</strong> saliva alone (Sukasaem et al. 2006; Huang &<br />

Tantbironj 2008). Topical application of TM reduces<br />

the extent of softening and mineral loss caused by<br />

subsequent exposure to erosive beverages (Kallayathi<br />

et al. 2008).<br />

<strong>CPP</strong>-<strong>ACP</strong> has potential as an additive to acidic<br />

drinks to prevent dental erosion. A key factor in such<br />

an approach is to estimate the lowest concentration<br />

of <strong>CPP</strong>-<strong>ACP</strong> which can be added to erosive drinks to<br />

eliminate the risk of erosion to enamel. Past research<br />

work on this topic has explored this issue using<br />

Powerade, to which was added varying amounts<br />

of <strong>CPP</strong>-<strong>ACP</strong> from 0.063% up to 0.25%. Analysis of<br />

the surface characteristics of enamel slabs in the<br />

laboratory setting using stereomicroscopy, scanning<br />

electron microscopy and surface profilometry<br />

demonstrated that adding <strong>CPP</strong>-<strong>ACP</strong> at 0.25% raised<br />

the pH from 2.70 to 3.90, and lowered the titratable<br />

acidity from 1.83 to 1.36). Enamel loss from etching<br />

reduced from 3.87µm to 0.19µm, which was identical<br />

to enamel samples kept in distilled water (0.25µm).<br />

A reduction in the erosive step defect occurred at<br />

concentrations down to 0.09%. Overall, the erosive<br />

potential of Powerade was attenuated or eliminated<br />

completely by the addition of low concentrations of<br />

<strong>CPP</strong>-<strong>ACP</strong> (Ramalingham et al. 2002 & 2005).<br />

There is also interest in including <strong>CPP</strong>-<strong>ACP</strong> in dental<br />

materials, such as glass ionomer cements (Mazzaoui<br />

et al. 2003) and zinc oxide non-eugenol temporary<br />

References<br />

O. ADEBAYO, M. BURROW, and M. TYAS. SEM<br />

evaluation of casein phosphopeptide-amorphous<br />

calcium phosphate-treated and conditioned<br />

enamel. J Dent Res 87(Spec Iss C):1, 2008A.<br />

O.A. ADEBAYO, M.F. BURROW, and M.J.<br />

TYAS. Dentine bonding after <strong>CPP</strong>-<strong>ACP</strong> paste<br />

treatment <strong>with</strong> and <strong>with</strong>out conditioning. J Dent<br />

36(12):1013-1024, 2008B.<br />

O.A. ADEBAYO, M.F. BURROW, and M.J. TYAS.<br />

An SEM evaluation of conditioned and bonded<br />

enamel following carbamide peroxide bleaching<br />

and casein phosphopeptide-amorphous calcium<br />

phosphate (<strong>CPP</strong>-<strong>ACP</strong>) treatment. J Dent<br />

37(4):297-306, 2009.<br />

O.A. ADEBAYO, M.F. BURROW, and M.J. TYAS.<br />

Resin-dentine interfacial morphology following<br />

<strong>CPP</strong>-<strong>ACP</strong> treatment. J Dent 38(2):96-105, 2010.<br />

C. AMORNPIPITHKUL, S. SANGUANSIN, and<br />

P. LEELATAWEEWUD. The Effects of Casein-<br />

Phosphopeptide-Amorphous-Calcium-Phosphate<br />

Paste on Plaque Calcium and Phosphate. J Dent<br />

Res 88(Spec Iss C):190, 2009.<br />

A. ANDERSSON, S. TWETMAN, K. SKÖLD-<br />

LARSSON, and L.G. PETERSSON. Lesion<br />

regression <strong>with</strong> <strong>CPP</strong>/<strong>ACP</strong>-containing cream<br />

assessed by laser fluorescence. J Dent Res<br />

85(Spec Iss B):2539, 2006.<br />

A. ANDERSSON, K. SKÖLD-LARSSON,<br />

cements used in crown and bridgework. Both lines<br />

of investigation have been followed, <strong>with</strong> the logic<br />

being to provide greater resistance to mineral loss<br />

at restoration margins, and reduced permeability of<br />

cut dentine beneath temporary crowns, respectively.<br />

Addition of up to 8.0% <strong>CPP</strong>-<strong>ACP</strong> into zinc oxide<br />

cements appears to be viable in terms of the<br />

compressive strength and film thickness achieved<br />

(Wong et al. 2006).<br />

A particularly interesting application of TM is the<br />

management of pathological tooth wear from acid<br />

regurgitation or severe bruxism (Meyers 2008).<br />

As well as prevebting dental erosion, laboratory<br />

studies suggest that frequent application of TM<br />

reduces enamel wear under conditions simulating<br />

bruxism and acid regurgitation, probably due to its<br />

lubrication properties (Ranjitkar et al. 2006, 2007,<br />

2008, 2009A&B). TM is able to reduce abrasive and<br />

acid-accelerated dentine wear (Narayana et al. 2006),<br />

supporting the use for TMP in patients <strong>with</strong> severe<br />

tooth wear from these differing causal pathways.<br />

Benefit has also been suggested for prevention of<br />

erosion from frequent consumption of wine (Piekarz<br />

et al. 2008).<br />

About the author:<br />

Professor LAURENCE WALSH BDSc<br />

PhD DDSc <strong>GC</strong>Ed FFOP(RCPA) FICD<br />

FPFA Laurence Walsh is Professor<br />

of Dental Science and Head of<br />

the School of Dentistry at the<br />

University of Queensland. He is a<br />

dental specialist in special needs<br />

dentistry and maintains a part time clinical practice<br />

in that field. Laurence is actively involved in the<br />

dental profession at a range of levels both nationally<br />

and internationally and has been involved in the<br />

development and assessment of chair-side diagnostic<br />

tools which use saliva and dental plaque. He is<br />

currently involved in studies of novel approaches for<br />

remineralisation of enamel and caries prevention.<br />

A. HALLGREN, L.G. PETERSSON and S.<br />

TWETMAN. Effect of a dental cream containing<br />

amorphous cream phosphate complexes on<br />

white spot lesion regression assessed by laser<br />

fluorescence. Oral Health Prev Dent 7;5(3):229-<br />

233, 2007.<br />

A.G. ANTONIO, V. PIERRO, and L.C. MAIA.<br />

Xylitol-based candies/lozenges: What is the<br />

evidence for caries-preventive effects? J Dent<br />

Res 88(Spec Iss A):2528, 2009.<br />

S. ARDU, N.V. CASTIONI, N. BENBACHIR, and<br />

I. KREJCI. Minimally invasive treatment of white<br />

spot enamel lesions. Quintessence Int 38(8):633-<br />

636, 2007.<br />

clinical corner<br />

23


D.G. AUGUSTSON, D. TANTBIROJN, and<br />

A. VERSLUIS. Recovery of Enamel Surface<br />

Hardness after Hydrochloric Acid Erosion. J Dent<br />

Res 89(Spec Iss B):4187, 2010.<br />

Z. AYTEPE, E.B. TUNA, D. ONER OZDAS, and<br />

E. YAMAC. Effect of <strong>CPP</strong>-<strong>ACP</strong> on Oral Health of<br />

Cerebral Palsy Children. J Dent Res 87(Spec<br />

Iss B):3343, 2008.<br />

D.L. BAILEY, G.G. ADAMS, C.E. TSAO, A.<br />

HYSLOP, K. ESCOBAR, D.J. MANTON, E.C.<br />

REYNOLDS and M.V. MORGAN. Regression<br />

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cream. J Dent Res 88(12):1148-1153, 2009.<br />

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and C. PRATI. Supplementation of Molar Incisor<br />

Hypoplasia Affected Teeth: SEM/EDX study. J<br />

Dent Res 89(Spec Iss B):3845, 2010.<br />

S.M. BEHNAN, A.O. ARRUDA, H. HASSON,<br />

W. SOHN, C. GONZÁLEZ-CABEZAS, and M.C.<br />

PETERS. J Dent Res 88(Spec Iss A):2051,<br />

2009.<br />

A.K. BURWELL, and D. MUSCLE. Sustained<br />

Calcium Ion and pH Release from Calcium<br />

Phosphate-Containing Dentifrices. J Dent Res<br />

88(Spec Iss A):1936, 2009.<br />

F. CAI, Y. YUAN, C. REYNOLDS, and E.<br />

REYNOLDS. Water soluble calcium, phosphate<br />

and fluoride of various dental products. J Dent<br />

Res 88(Spec Iss B):57, 2009.<br />

F. CAI, P. SHEN, M.V. MORGAN, and E.C.<br />

REYNOLDS: <strong>Remineralization</strong> of enamel<br />

subsurface lesions<br />

in situ by sugar-free lozenges containing casein<br />

phosphopeptide-amorphous calcium phosphate.<br />

Aust Dent J 48(4): 240-243, 2003.<br />

P.C. CARUANA, S.A. MULAIFY, R. MOAZZEZ<br />

and D BARTLETT. The effect of casein and<br />

calcium containing paste on plaque pH following<br />

a subsequent carbohydrate challenge. J Dent<br />

37(7):522-526, 2009.<br />

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Different Ways of Applying <strong>GC</strong>-Dentifrice to<br />

Reduce Tooth Tissue Loss. J Dent Res 89(Spec<br />

Iss B):4793, 2010.<br />

N.J. COCHRANE, F. CAI, and E.C. REYNOLDS.<br />

QLF and TMR analysis of <strong>CPP</strong>-ACFP<br />

remineralized enamel in vitro. J Dent Res<br />

85(Spec Iss B):0192, 2006.<br />

N.J. COCHRANE, and E. REYNOLDS. Enamel<br />

Remineralisation <strong>with</strong> Casein Phosphopeptidestabilised<br />

Amorphous Calcium Fluoride<br />

Phosphate Complexes. J Dent Res 87(Spec Iss<br />

B):51, 2008.<br />

N.J. COCHRANE, R.J. MAYNE, S. RATNESER,<br />

M.G. WOODS, and E.C. REYNOLDS. Enamel<br />

Remineralisation Reduced Iatrogenic Enamel<br />

Damage During Orthodontic Adhesive Removal.<br />

J Dent Res 89(Spec Iss B):3647, 2010.<br />

K.J. CROSS, T.J. ATTARD, N.L. HUQ, and E.C.<br />

REYNOLDS. Structure and 15N-Dynamics of<br />

Casein Phosphopeptide-Amorphous Calcium<br />

Phosphate Nanocomplexes. J Dent Res<br />

85(Spec Iss B):2534, 2006.<br />

K.J. CROSS, N.L. HUQ and E.C. REYNOLDS.<br />

Casein phosphopeptides in oral healthchemistry<br />

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Y. DUAN, G. WANG, B. MATIS, X. CHENG,<br />

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I. ELSAYAD, A. SAKR and Y. BADR.<br />

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Casein Phosphopeptide Paste: Effect on Enamel<br />

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S. KARIYA, T. SATO, Y. SAKAGUCHI, and E.<br />

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V.L. KUMAR, A. ITTHAGARUN and N.M. KING.<br />

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of root surface erosion and root surface caries.<br />

PhD thesis, University of Queensland, Brisbane,<br />

2007.<br />

J. VLACIC, I.A. MEYERS and L.J.WALSH.<br />

Combined <strong>CPP</strong>-<strong>ACP</strong> and photoactivated<br />

disinfection (PAD) therapy in arresting root<br />

surface caries: a case report. Brit Dent J<br />

203(8):457-459, 2007.<br />

G.D. WALKER, F. CAI, P. SHEN, D.L. BAILEY,<br />

Y, YUAN, N.J. COCHRANE, C. REYNOLDS<br />

and E.C. REYNOLDS. Consumption of milk<br />

<strong>with</strong> added casein phosphopeptide-amorphous<br />

calcium phosphate remineralizes enamel<br />

subsurface lesions in situ. Aust Dent J 54(3):245-<br />

249, 2009.<br />

L.J. WALSH. Tooth Mousse Portfolio. <strong>GC</strong> Asia<br />

Dental Pte Ltd, Singapore, 2003.<br />

L.J. WALSH. Tooth Mousse Portfolio 2. <strong>GC</strong> Asia<br />

Dental Pte Ltd, Singapore, 2004.<br />

L.J. WALSH. Tooth Mousse: Anthology of<br />

Applications, <strong>GC</strong> Asia Dental Pte Ltd, Singapore,<br />

2007.<br />

L.J. WALSH. The effects of <strong>GC</strong> Tooth Mousse on<br />

cervical dentinal sensitivity: a controlled clinical<br />

trial. Internat Dent (Australas Edn) 5(1):16-23,<br />

2010.<br />

L.J. WALSH, W.S. WANG, A. CAKAR, C.<br />

DEVANI, K.K. TRAN, and A. HALL. Effect of<br />

<strong>CPP</strong>-<strong>ACP</strong> versus Potassium Nitrate on Cervical<br />

Dentinal Hypersensitivity. J Dent Res 85(Spec<br />

Iss B):0947, 2006.<br />

R. WONG, J. PALAMARA, and P.R. WILSON.<br />

Incorporation of Casein Phosphopeptide-<br />

Amorphous Calcium Phosphate into a Temporary<br />

Cement. J Dent Res 85(Spec Iss B):0653, 2006.<br />

R.H. WONG, A.W. WONG, D. SIVAPALAN,<br />

M.H. NGUYEN, A.M. HO, A.S. WANG, and S.E.<br />

LAU. Penetration of Bleaching Agents in Tooth<br />

MousseTM Treated Bovine Incisors. J Dent Res<br />

89(Spec Iss B):4019, 2010.<br />

K. YAMAGUCHI, M. MIYAZAKI, T.<br />

TAKAMIZAWA, H INAGE and B.K. MOORE.<br />

Effect of <strong>CPP</strong>-<strong>ACP</strong> paste on mechanical<br />

properties of bovine enamel as determined by an<br />

ultrasonic device. J Dent 34(3):230-236, 2006.<br />

E. YASUDA, T. SATO, S. KATO, L. CHEN, and<br />

E. YOSHII. Comparative Study on <strong>CPP</strong>-<strong>ACP</strong> and<br />

TCP Based Products. J Dent Res 89(Spec Iss<br />

A):317, 2010.<br />

O. YAZICIOGLU, B. YAMAN, A. GULER, R.<br />

ASIYEV, and F. KORAY. Quantitative Evaluation<br />

of the Effect <strong>CPP</strong>-<strong>ACP</strong> on Enamel Caries. J Dent<br />

Res 89(Spec Iss B):3232, 2010.<br />

V. YENGOPAL and S. MICKENAUTSCH.<br />

Casein Phosphopeptide-Amorphous Calcium<br />

Phosphate (<strong>CPP</strong>-<strong>ACP</strong>) – a Systematic Review. J<br />

Dent Res 85(Spec Iss C): 010, 2006.<br />

V. YENGOPAL and S. MICKENAUTSCH. Caries<br />

preventive effect of casein phosphopeptideamorphous<br />

calcium phosphate (<strong>CPP</strong>-<strong>ACP</strong>): a<br />

meta-analysis. Acta Odontol Scand 21:1-12,<br />

2009.<br />

Q. XIE, C.D. WU, and A.K.B. BEDRAN-RUSSO.<br />

<strong>Remineralization</strong> Effects of <strong>CPP</strong>-<strong>ACP</strong> and<br />

Proanthocyanidin on Artificial Root Caries. J<br />

Dent Res 86(Spec Iss A):0512, 2007.<br />

C.H. ZHOU, X.H. SUN, X.C. ZHU.<br />

Quantification of remineralized effect of casein<br />

phosphopeptiode-amorphous calcium phosphate<br />

on post-orthodontic white spot lesion. Shanghai<br />

Kou Qiang Yi Xue 18(5): 449-454, 2009.<br />

clinical corner<br />

25


A closer look at remineralisation and <strong>CPP</strong>-<strong>ACP</strong><br />

As a publication, MID believes in the importance of informing dentists about the<br />

evidence available on MI topics so they can make scientifically sound choices in the<br />

treatment of their patients. In the research-clinical application jigsaw puzzle, it is<br />

essential to make all the pieces fit in order to see the whole picture.<br />

This process is outlined in the flow diagram below<br />

Systematic review -> academic explanation -> clinical application<br />

Systematic Review<br />

Title: Caries preventive effect of casein phosphopeptideamorphous<br />

calcium phosphate (<strong>CPP</strong>-<strong>ACP</strong>): a meta-analysis<br />

Objective. This systematic review <strong>with</strong> meta-analyses<br />

sought to answer the following question: ‘‘Does <strong>CPP</strong>-<strong>ACP</strong><br />

[casein phosphopeptide-amorphous calcium phosphate],<br />

when introduced into the oral environment, provide any<br />

caries-preventive benefit superior to that of any other<br />

intervention or placebo?’’<br />

Material and methods. Seven electronic databases were<br />

searched for trials relevant to the review question. Twelve<br />

articles were accepted after application of inclusion and<br />

exclusion criteria.<br />

Results. Of the accepted articles, five in situ<br />

randomized control trials (RCT) could be pooled for metaanalyses.<br />

During the short-term (7_21 days) in situ trials,<br />

participants wore appliances containing enamel slabs that<br />

were analyzed in the laboratory after exposure to <strong>CPP</strong>-<br />

<strong>ACP</strong>. The pooled in situ results showed a weighted mean<br />

difference (WMD) of the percentage remineralization<br />

scores in favor of chewing gum <strong>with</strong> 18.8 mg <strong>CPP</strong>-<strong>ACP</strong> as<br />

compared to chewing gum <strong>with</strong>out <strong>CPP</strong>-<strong>ACP</strong> (WMD _8.01;<br />

95% CI: _10.54 to _5.48; p_0.00001), as well as compared<br />

to no intervention (WMD_13.56; 95% CI: _16.49 to _10.62;<br />

p_0.00001). A significant higher remineralization effect<br />

was also observed after exposure to 10.0 mg <strong>CPP</strong>-<strong>ACP</strong><br />

(_7.75; 95% CI: _9.84 to _5.66; p_0.00001). One long-term<br />

in vivo RCT (24 months) <strong>with</strong> a large sample size (n_2720)<br />

found that the odds of a tooth surface’s progressing to<br />

caries was 18% less in subjects who chewed sugar-free<br />

gum containing 54 mg <strong>CPP</strong>-<strong>ACP</strong> than in control subjects<br />

who chewed gum <strong>with</strong>out <strong>CPP</strong>-<strong>ACP</strong> (p_ 0.03).<br />

Conclusion. Within the limitations of this systematic<br />

review <strong>with</strong> meta-analysis, the results of the clinical in<br />

situ trials indicate a short-term remineralization effect of<br />

<strong>CPP</strong>-<strong>ACP</strong>. Additionally, the promising in vivo RCT results<br />

suggest a caries preventing effect for long-term clinical<br />

<strong>CPP</strong>-<strong>ACP</strong> use. Further randomized control trials are<br />

needed in order to confirm these initial results in vivo.<br />

Article details :<br />

Yengopal V, Mickenautsch S. Caries preventive effect of<br />

casein phosphopeptide-amorphous calcium phosphate<br />

(<strong>CPP</strong>-<strong>ACP</strong>): a meta-analysis. Acta Odontol Scand 2009; 67:<br />

321-32.<br />

The academic explanation<br />

Dr Steffen Mickenautsch,<br />

academic researcher in<br />

Johannesburg, South Africa<br />

MID: Of all the studies available<br />

on this subject, why were you<br />

only able to use 5 for your meta<br />

analysis?<br />

Steffen Mickenautsch: Firstly, we<br />

had to exclude other studies because they were either:<br />

conducted in the laboratory and not in the clinic; done on<br />

animal and not on human tissue or did not compare <strong>CPP</strong>-<br />

<strong>ACP</strong> against anything else.<br />

The problem <strong>with</strong> studies from the laboratory is that<br />

one really cannot be sure that the results would be the<br />

same in the ‘real’ world. The same is valid when studying<br />

the effect of treatments on animal tissue. The results of<br />

either are important to justify whether studies should be<br />

conducted on patients or not, because it is not ethical<br />

to study new treatments on humans if laboratory and/<br />

or animal studies show that these are not successful.<br />

Therefore, laboratory and/or animal studies are important<br />

first steps for testing new drugs or treatments before they<br />

can be allowed to be tested on humans. However, in our<br />

systematic review we wanted to know whether <strong>CPP</strong>-<br />

<strong>ACP</strong> is beneficial for clinical use on patients and neither,<br />

laboratory nor animal studies, can answer this question.<br />

That is why we had to exclude them.<br />

Clinical studies that fail to compare a new type of<br />

treatment against another, (preferably the type of standard<br />

treatment commonly used to date) are unable to answer<br />

the question whether the new treatment is better, the same<br />

or worse. But this was exactly what we were trying to find<br />

out, thus we could not include these types of studies either.<br />

After all these considerations we had 11 studies<br />

available to work <strong>with</strong>. From these, 5 were similar enough<br />

to be combined in a meta-analysis. A meta-analysis is a<br />

statistical method by which the separate results of several<br />

studies are combined to one average result. However, in<br />

order to be able to do this the studies need to be similar,<br />

e.g. in their methods and outcomes, before they can be<br />

combined. Otherwise the meta-analysis would produce<br />

meaningless results.<br />

26 evidence<br />

mi.gceurope.com


We reviewed the other 6 studies separately in our<br />

systematic review <strong>with</strong>out including them in the metaanalysis.<br />

MID: What criteria did the 5 that you selected meet and<br />

why is this important?<br />

Steffen Mickenautsch: These 5 studies compared <strong>CPP</strong>-<br />

<strong>ACP</strong> against other types of treatments. They provided<br />

information on how well each, the <strong>CPP</strong>-<strong>ACP</strong> and the other<br />

treatment worked on patients and then compared both<br />

results to find out which one was better. This was exactly<br />

what we needed to know. In addition, they all fulfilled the<br />

requirements for meta-analysis; they all used <strong>CPP</strong>-<strong>ACP</strong> in<br />

dental chewing gum; they included the same <strong>CPP</strong>-<strong>ACP</strong><br />

concentration; study length and used the same type of<br />

other treatment for comparison.<br />

MID: Please explain your introduction: “The advantages<br />

of meta-analysis over qualitative synthesis is that it<br />

provides the opportunity to identify a treatment effect as<br />

statistically significant (p


MID: In your conclusion it states that this meta<br />

analysis shows that <strong>CPP</strong>-<strong>ACP</strong> does have a short term<br />

remineralising effect – what should a practising dentist<br />

who reads this understand about this statement?<br />

Steffen Mickenautsch: If a patient is identified to have a<br />

high caries activity or a high risk to develop cavities in the<br />

near future, the established short-term effect promises<br />

that <strong>CPP</strong>-<strong>ACP</strong> is able to stop the further progression of<br />

(non-cavitated) carious lesions and is able to prevent the<br />

development of such. Therefore, <strong>CPP</strong>-<strong>ACP</strong> may be used<br />

as one immediate intervention in the treatment of such<br />

patients.<br />

MID: You also looked at one study that examined the<br />

long-term effect of <strong>CPP</strong>-<strong>ACP</strong> – what were the important<br />

elements of this particular study?<br />

Steffen Mickenautsch: In that study, patients were given<br />

<strong>CPP</strong>-<strong>ACP</strong> containing chewing gum over the period of 2<br />

years and were compared to similar patients that chewed<br />

sugar-free chewing gum <strong>with</strong>out <strong>CPP</strong>-<strong>ACP</strong>. The result<br />

showed that patients using the <strong>CPP</strong>-<strong>ACP</strong> containing gum<br />

had 18% lesser likelihood of caries progression. This result<br />

was statistically significant, thus very unlikely to be a<br />

coincident. All patients had active caries and the <strong>CPP</strong>-<strong>ACP</strong><br />

gum showed to be more effective to stop further progress<br />

of the existing carious lesions. In that regard one has to<br />

remember that sugar-free chewing gum is considered<br />

to be effective against caries too. That means, that the<br />

group of patients <strong>with</strong>out the <strong>CPP</strong>-<strong>ACP</strong> would have also<br />

experienced an anticaries effect. Only, this effect was<br />

observed to be larger in the <strong>CPP</strong>-<strong>ACP</strong> group.<br />

MID: Is this systematic review conclusive or is more<br />

research needed?<br />

Steffen Mickenautsch: From an academic point of view,<br />

the current knowledge about <strong>CPP</strong>-<strong>ACP</strong> allows us to be<br />

optimistic about the claim that <strong>CPP</strong>-<strong>ACP</strong> is effective<br />

against caries. The currently available studies provide<br />

evidence that this claim is not only plausible but also<br />

tends to prove it to be correct rather than disproving it. To<br />

have more high quality research will be of advantage to<br />

validate and strengthen this claim even further.<br />

“In my practice the compliance rate and repurchase<br />

of the Tooth Mousse / Mi paste has<br />

been very high, and this indicates to me that<br />

the patients are happy <strong>with</strong> the results, and<br />

find value in the products.”<br />

Andrew Brostek<br />

The clinical application<br />

Dr Andrew Brostek, private<br />

dentist in Perth, Australia<br />

MID: For how many years have you<br />

been using Tooth Mousse/MI Paste<br />

in your practice?<br />

Andrew Brostek: I began soon<br />

after it was first made available in<br />

Australia, but have used it more<br />

intensively in the last three years.<br />

MID: What factors made you decide to start using it in<br />

your practice and recommend it to your patients in the<br />

first place?<br />

Andrew Brostek: After being exposed to the information<br />

about <strong>CPP</strong>-<strong>ACP</strong> presented at several Continuing Education<br />

courses, and then reading some of the early studies<br />

published by Professor Eric Reynolds and his University<br />

of Melbourne research group, I realised that using<br />

the products containing <strong>CPP</strong>-<strong>ACP</strong> (<strong>GC</strong> Tooth Mousse<br />

/ Mi Paste, Tooth Mousse Plus (<strong>CPP</strong>-ACFP) and the <strong>GC</strong><br />

Recaldent chewing gum) had great potential to benefit<br />

my patients.<br />

MID: After reading the abstract of the meta-analysis<br />

on the remineralising effect of <strong>CPP</strong>-<strong>ACP</strong>, how will this<br />

affect the way in which you use and prescribe Tooth<br />

Mousse/MI Paste in your practice, if at all?<br />

Andrew Brostek: The publication of this meta-analysis<br />

review reinforces my own belief in the effectiveness of<br />

<strong>CPP</strong>-<strong>ACP</strong>, based on my own clinical experiences <strong>with</strong><br />

compliant patients. Evidence based dentistry is essential<br />

to guide clinicians in improving treatment protocols, and<br />

I await further data from in vivo trials to confirm these<br />

results. In terms of prescribing, I use the fluoride versions<br />

<strong>CPP</strong>-ACFP i.e. Tooth Mousse Plus/ Mi Paste Plus for high<br />

risk patients over the age of 7 years, as study results show<br />

an increased lesion preventive effect <strong>with</strong> the fluoride<br />

combination. I usually prescribe nightly application of a<br />

pea-sized amount of the Tooth Mousse Plus / Mi paste<br />

Plus (immediately before bed), but in very high caries<br />

rate patients, I prescribe both a morning and nightly<br />

application, <strong>with</strong> concomitant use of Recaldent gum<br />

at least twice per day (10 minutes per application). As<br />

evidenced by studies, chewing the <strong>CPP</strong>-<strong>ACP</strong> gum, three<br />

times per day was very effective in caries-rate reduction.<br />

MID: Do you find this meta-analysis easy to interpret,<br />

in terms of applying this to your daily practice?<br />

Andrew Brostek: My understanding of the value of metaanalysis<br />

is to provide a more objective assessment of the<br />

available statistically significant literature. So yes, it does<br />

have value to me in suggesting improved protocols. Again<br />

28 evidence<br />

mi.gceurope.com


Patient <strong>with</strong> extensive white spot lesions After two months, showing partial remineralisation after<br />

twice daily application of <strong>CPP</strong>-<strong>ACP</strong><br />

speaking as a full-time clinician, I am very interested in any<br />

improvement in caries-preventive benefit and particularly<br />

in achieving enamel remineralisation.<br />

My daily practice protocols vary depending on the<br />

patient lesion presentation. For poor compliance patients<br />

<strong>with</strong> rampant caries, I mainly rely on prescribing twicedaily<br />

brushing <strong>with</strong> a high-dose fluoride (5000 ppm)<br />

toothpaste, and clinician-applied fluoride varnish at recall.<br />

The prevention of demineralisation by the use of high<br />

concentrations of fluoride is of critical importance in our<br />

anti-caries chemical armentarium.<br />

But for compliant high-risk patients <strong>with</strong> multiple early<br />

lesions (white-spot lesions) I use a slightly different protocol<br />

emphasising the use of <strong>CPP</strong>-<strong>ACP</strong>. To achieve increased<br />

remineralisation of these white spot lesions, especially<br />

in younger people <strong>with</strong> unaesthetic anterior lesions, I<br />

prescribe daily <strong>CPP</strong>-<strong>ACP</strong> (or <strong>CPP</strong>-ACFP) Tooth Mousse / Mi<br />

Paste application, in combination <strong>with</strong> twice-daily tooth<br />

brushing <strong>with</strong> a lower fluoride concentration (1000 ppm)<br />

toothpaste. This allows greater sub-surface remineralisation<br />

of non-cavitated lesions, evidenced over time by the<br />

reversal of the white-spot appearance. Unfortunately<br />

utilising a higher 5000 ppm fluoride toothpaste will seal<br />

off the unaesthetic surface scar rapidly, not allowing the<br />

deeper subsurface remineralisation to occur. Of course,<br />

regular effective plaque removal, diet and lifestyle<br />

modification, normal saliva quality and quantity, are all<br />

important factors in modifying the disease risk and aiding<br />

in tooth remineralisation.<br />

MID: As a busy clinician, how do you keep yourself<br />

updated on developments in clinical evidence in<br />

dentistry, particularly in MID?<br />

Andrew Brostek: That’s a tough question, as most<br />

of us are fairly busy in our own dental practices. The<br />

role of Continuing Education courses is important and<br />

attendance is compulsory in Australia. Belonging to<br />

various professional dental bodies helps, as it entitles you<br />

to some dental journal subscriptions, and staying current<br />

is important. I think that allows most of us to entertain our<br />

own specific dental interests.<br />

MID: Some dental academics say that clinicians and the<br />

practice-based evidence they record is very important<br />

in filling the gaps left by academic research studies.<br />

Have you captured and recorded any interesting data<br />

on remineralisation <strong>with</strong> Tooth Mousse/MI Paste since<br />

you’ve started using it? If so, what are some of the<br />

most interesting trends that you’ve noticed?<br />

Andrew Brostek: I find recording practice-based<br />

evidence hard to do in a typical busy day. Many of you<br />

may identify <strong>with</strong> my daily problems, where some patients<br />

come late to appointments, or extra ‘pain’ patients are<br />

over-booked into an already busy schedule. My main<br />

contribution is to have my dental camera handy to<br />

document any interesting dental issues quickly.<br />

My belief in <strong>CPP</strong>-<strong>ACP</strong> has been reinforced by observing<br />

non-cavitated white-spot lesions becoming remineralised<br />

over periods of between six weeks and 3 months <strong>with</strong><br />

regular daily use of the Tooth Mousse / Mi paste by<br />

the patient. Progress is easy to observe, as the lesions<br />

change from the surface white scar to a relatively normal<br />

tooth appearance. The clinical protocol I use to achieve<br />

this is quite simple: The enamel lesion is etched <strong>with</strong><br />

phosphoric acid for 10 seconds and then Tooth Mousse /<br />

Mi Paste is immediately applied. The patient then applies<br />

the Tooth Mousse nightly until lesion reversal occurs. In<br />

difficult cases, I might re-etch at one-month recall, or<br />

even additionally at the two-month recall, to aid <strong>CPP</strong>-<strong>ACP</strong><br />

penetration by removing surface protein from the enamel.<br />

In my practice the compliance rate and re-purchase<br />

of the Tooth Mousse / Mi paste has been very high, and<br />

this indicates to me that the patients are happy <strong>with</strong><br />

the results, and find value in the products. Many of the<br />

mothers are also using the <strong>CPP</strong>-<strong>ACP</strong> products on their<br />

younger children’s teeth for caries prevention.<br />

In conjunction <strong>with</strong> our individual patient caries risk<br />

assessment protocols (diet /lifestyle analyses, and the use<br />

of saliva and plaque testing on select patients) and then<br />

specific treatment targeting (such as the use of <strong>CPP</strong>-<strong>ACP</strong>),<br />

my dental hygienists and I believe we are benefitting our<br />

patients, and practising modern 21st century dentistry.<br />

evidence<br />

29


MI toolkit<br />

1<br />

30 mi toolkit<br />

mi.gceurope.com<br />

2<br />

4


What’s inside the tube?<br />

Tooth Mousse, also known as MI Paste in<br />

some regions of the world, is considered the<br />

number one remineralizing paste that is<br />

backed by sound scientific evidence.<br />

For low to medium risk patients, MI Paste<br />

or Tooth Mousse is recommended. However,<br />

for patients <strong>with</strong> high risk, MI Paste<br />

Plus/Tooth Mousse Plus contains<br />

additional 900ppm Flouride and<br />

is therefore better suited to<br />

their oral health requirements.<br />

3<br />

Studies that prove the clinical superiority of <strong>GC</strong> Tooth<br />

Mousse/MI Paste are:<br />

z The only remineralizing cream <strong>with</strong> proven a scientific<br />

record <strong>with</strong> more then 200 scientific references<br />

and having sold material for more than 160 million<br />

applications worldwide since the original Australasian<br />

introduction in 2002<br />

Abstract 3645 - IADR 2010, Barcelona, Spain. Comparison of Tooth<br />

Mousse (MI Paste) <strong>with</strong> Clinpro in situ. E Reynolds, F Cai, P. Shen, G<br />

Walker, Y Yuan, N Cochrane, D Manton, C Reynolds. Oral Health CRC,<br />

Melbourne Dental School, University of Melbourne, Australia<br />

z Searching from 7 databases and about 3500 articles, it<br />

has been concluded that Tooth Mousse/MI Paste Plus<br />

does <strong>Remineralization</strong> and has Caries protection effect.<br />

V. YENGOPAL & S. MICKENAUTSCH. University of the Witwatersrand,<br />

South Africa. Acta Odontologica Scandinavica 2009<br />

Click on the numbers to learn more<br />

1. <strong>GC</strong> Tooth Mousse offers Three-in-One solution<br />

5<br />

2. Uses for Tooth Mousse/MI Paste<br />

mi toolkit<br />

3. Contraindications<br />

4. Application methods<br />

5. Packaging<br />

6. Additional instructions<br />

6<br />

31


The Science behind Remin<br />

The only Reminaralizing cream <strong>with</strong> proven a Scientific record <strong>with</strong> more then 200<br />

scientific references and having sold material for more than 160 million applications<br />

worldwide since the original Australasian introduction in 2002*<br />

Articles identified through<br />

keyword search in<br />

databases (n=3459)<br />

Articles included for more<br />

detailed review (n=35)<br />

Articles accepted (n=12)<br />

Randomized control trials<br />

(n=11)<br />

Randomized control trials<br />

included in meta-analysis<br />

(n=5)<br />

Articles <strong>with</strong>out relevance<br />

to review questions<br />

excluded (n=3424)<br />

Articles excluded due<br />

to non-compliance <strong>with</strong><br />

exclusion criteria (n=3424)<br />

Systematic review (n=1)<br />

Randomized control trials<br />

not included in metaanalysis<br />

(n=6)<br />

Searching from 7 databases and about 3500 articles, it has been concluded that Tooth Mousse/MI<br />

Paste Plus does <strong>Remineralization</strong> and has Caries protection effect.*<br />

*V. YENGOPAL & S. MICKENAUTSCH. University of the Witwatersrand, South Africa. Acta Odontologica Scandinavica 2009<br />

32 mi toolkit<br />

mi.gceurope.com


PLACEBO<br />

RECALDENT HIGH FLOURIDE PRODUCTS<br />

PLACEBO PASTE<br />

1000PPM F PASTE<br />

CLINPRO<br />

5000PPM F PASTE<br />

TOOTH MOUSSE<br />

MI PASTE PLUS<br />

Notice no change in the demineralised White<br />

Spot Lesion after the use of a Placebo Paste<br />

Notice the hard hypermineralised layer<br />

formed due to the very high fluoride ppm,<br />

this acts like a hard shell preventing the<br />

<strong>Remineralization</strong> of the underlying White<br />

Spot Lesion lesion.<br />

Concluding that Ca and PO4 are the most<br />

crucial elements for <strong>Remineralization</strong> and<br />

Fluoride only acts as a catalyst.<br />

Notice no Hard impervious layer as compared<br />

to High Fluoride containing products.<br />

Tooth Mousse and MI Paste Plus show a<br />

uniform <strong>Remineralization</strong> of the Enamel and<br />

Dentine structures. However, MI Paste Plus<br />

shows higher <strong>Remineralization</strong> due to the fact<br />

that Fluoride acts as a catalyst to encourage<br />

Calcium and Phosphate to enter inside the<br />

Tooth structure<br />

*Abstract 3645 - IADR 2010, Barcelona, Spain. Comparison of Tooth Mousse (MI Paste) <strong>with</strong> Clinpro in situ. E Reynolds, F Cai, P. Shen, G Walker,<br />

Y Yuan, N Cochrane, D Manton, C Reynolds. Oral Health CRC, Melbourne Dental School, University of Melbourne, Australia<br />

mi toolkit<br />

33


minimum intervention, maximum return<br />

mid<br />

Issue 3

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