28.01.2015 Views

Milk-and-Dairy-Products-in-Human-Nutrition-FAO

Milk-and-Dairy-Products-in-Human-Nutrition-FAO

Milk-and-Dairy-Products-in-Human-Nutrition-FAO

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

128<br />

<strong>Milk</strong> <strong>and</strong> dairy products <strong>in</strong> human nutrition<br />

4.4.4 Bone-remodell<strong>in</strong>g transient<br />

The bone remodell<strong>in</strong>g transient is a temporary alteration <strong>in</strong> the balance between<br />

bone formation <strong>and</strong> bone resorption brought about by any factor (e.g. drugs,<br />

hormones or nutrients that alter either secretion of parathyroid hormone 25 or its<br />

action on bone) that affects bone remodell<strong>in</strong>g (Heaney, 2001). Accord<strong>in</strong>g to Heaney<br />

(2001), because the remodell<strong>in</strong>g activity is spread out over several months (several<br />

weeks <strong>in</strong> grow<strong>in</strong>g children, approximately three months <strong>in</strong> young adults <strong>and</strong> 6–18<br />

months <strong>in</strong> older adults), nutritional <strong>in</strong>terventions that alter remodell<strong>in</strong>g produce a<br />

temporary phase lag between the normally coupled destructive <strong>and</strong> constructive<br />

components of the bone-remodell<strong>in</strong>g process. This phase lag, when observed as an<br />

external balance or a dual-energy X-ray absorptiometry time course (commonly<br />

used to measure BMD), is the remodell<strong>in</strong>g transient. Steady-state effects of any<br />

given nutrient <strong>in</strong>take can only be ascerta<strong>in</strong>ed by measurements made after the<br />

transient has passed. The significance of the transient for nutritional <strong>in</strong>terventions is<br />

both that early effects will always be mislead<strong>in</strong>g <strong>and</strong> that one can draw no <strong>in</strong>ference<br />

whatsoever about the new steady state from what one observes dur<strong>in</strong>g the transient<br />

phase (Heaney, 2001).<br />

4.4.5 Limitations of studies us<strong>in</strong>g bone m<strong>in</strong>eral density as an end po<strong>in</strong>t<br />

BMD is used to def<strong>in</strong>e peak bone mass <strong>in</strong> young adults <strong>and</strong> is generally accepted to<br />

be a strong predictor of fractures <strong>in</strong> the elderly (see Bischoff-Ferrari et al., 2007).<br />

Bone m<strong>in</strong>eral content <strong>in</strong> adults at any time is dependent on peak bone density<br />

achieved dur<strong>in</strong>g development <strong>and</strong> subsequent bone loss; therefore, low BMD can<br />

result from poor bone accretion, accelerated bone loss or both (see Small, 2005 <strong>and</strong><br />

references there<strong>in</strong>). BMD is often used as a surrogate measure of efficacy <strong>in</strong> cl<strong>in</strong>ical<br />

trials of osteoporosis therapies because even though studies with fracture <strong>in</strong>cidence<br />

as a primary end po<strong>in</strong>t provide the most mean<strong>in</strong>gful assessment, these trials typically<br />

require large numbers of patients <strong>and</strong> often take at least three years to generate<br />

sufficient data (Small, 2005). Although the majority of cl<strong>in</strong>ical trials with calcium<br />

or dairy product supplementation <strong>in</strong> children <strong>and</strong> adolescents that have been completed<br />

to date show a positive effect of <strong>in</strong>tervention on bone mass, they are generally<br />

too short (one to three years) to address the question of whether it is the temporary<br />

adaptation of bone tissue to the alteration <strong>in</strong> calcium <strong>in</strong>take that leads to peak bone<br />

mass (Matkovic et al., 2005). The <strong>in</strong>crease <strong>in</strong> bone mass observed <strong>in</strong> those shortterm<br />

studies could be expla<strong>in</strong>ed to a large extent by the bone-remodell<strong>in</strong>g transient<br />

(see “Bone-remodell<strong>in</strong>g transient”, above). However, to conduct controlled feed<strong>in</strong>g<br />

trials for sufficiently long periods for bone properties to change may not be practical<br />

except for animal studies (Weaver, 2008).<br />

4.4.6 Osteoporosis<br />

Osteoporosis is a condition of low bone mass with <strong>in</strong>creased risk of fracture. Bones<br />

can get to that state through acquir<strong>in</strong>g low peak bone mass dur<strong>in</strong>g growth <strong>and</strong>/<br />

or through accelerated bone loss later <strong>in</strong> life as depicted <strong>in</strong> Figure 4.1. Worldwide<br />

25 Parathyroid hormone (PTH) regulates the quantity of remodel<strong>in</strong>g activity.

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!