01.12.2012 Views

MAGICAL MEDICINE: HOW TO MAKE AN ILLNESS ... - Invest in ME

MAGICAL MEDICINE: HOW TO MAKE AN ILLNESS ... - Invest in ME

MAGICAL MEDICINE: HOW TO MAKE AN ILLNESS ... - Invest in ME

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

1995<br />

123<br />

“The use of cardiopulmonary exercise test<strong>in</strong>g is not only valid and reliable, but also serves as an objective <strong>in</strong>dicator for<br />

assess<strong>in</strong>g disability. Maximal cardiopulmonary exercise test<strong>in</strong>g provides two objective markers of functional capacity.<br />

The first is maximal oxygen consumption. The most important determ<strong>in</strong>ant of functional capacity is not maximal<br />

oxygen consumption, but anaerobic threshold. Typically <strong>ME</strong>/CFS patients achieve less than 80% of predicted<br />

maximal oxygen consumption with an anaerobic threshold lower than 40% of predicted peak oxygen<br />

consumption levels. In <strong>ME</strong>/CFS patients, we have not found re‐condition<strong>in</strong>g to be possible. In fact, attempts to re‐<br />

condition patients consistently results <strong>in</strong> exacerbation of symptomatology. Cardiopulmonary exercise test<strong>in</strong>g<br />

can be used to provide <strong>ME</strong>/CFS patients with another objective marker that will aid them <strong>in</strong> obta<strong>in</strong><strong>in</strong>g disability<br />

status” (SR Steven. JCFS 1995:1:3‐4:127‐129).<br />

1996<br />

At the State of Massachusetts educational workshop given by Professor Paul Cheney, evidence was<br />

presented of the complexity of <strong>ME</strong>/CFS (referred to as “CFIDS”, or Chronic Fatigue and Immune<br />

Dysfunction Syndrome). Accord<strong>in</strong>g to Cheney, 80% of <strong>ME</strong>/CFS patients display medication and<br />

environmental sensitivities; there is evidence of lymphatic <strong>in</strong>volvement, with the thoracic duct be<strong>in</strong>g tender,<br />

and the swollen areas on the neck or upper chest be<strong>in</strong>g a back‐up of lymphatic fluid.<br />

Cheney biopsied 16 digits of people with <strong>ME</strong>/CFS and found a vasculitis not uncommon <strong>in</strong> immune<br />

activation and similar to that which is found <strong>in</strong> SLE / systemic lupus erythematosus (The Massachusetts<br />

CFIDS Update).<br />

1997<br />

“Myocarditis was a common symptom <strong>in</strong> an analysis of 1,000 patients of <strong>ME</strong>/CFS who were seen <strong>in</strong><br />

Glasgow over the past 20 years. We were struck by the often‐occurr<strong>in</strong>g association of patients who develop <strong>ME</strong>/CFS<br />

with acute chest pa<strong>in</strong> resembl<strong>in</strong>g a coronary thrombosis. On subsequent cl<strong>in</strong>ical follow‐up, all these patients had a<br />

cl<strong>in</strong>ical course that was <strong>in</strong>dist<strong>in</strong>guishable from patients who presented with Syndrome X. Nuclear magnetic resonance<br />

spectroscopy studies of skeletal muscle <strong>in</strong> patients with Syndrome X show abnormalities that are identical to those<br />

found <strong>in</strong> patients with <strong>ME</strong>/CFS. We, <strong>in</strong> exam<strong>in</strong><strong>in</strong>g muscle biopsies of patients with <strong>ME</strong>/CFS, showed an <strong>in</strong>crease <strong>in</strong><br />

calcium ATPase activity <strong>in</strong> skeletal muscles. These data strengthen the relationship between <strong>ME</strong>/CFS and Syndrome X<br />

and suggest that an <strong>in</strong>creased energy expenditure, with a consequent reduction of <strong>in</strong>tra‐cellular ATP (adenos<strong>in</strong>e<br />

triphosphate) and an <strong>in</strong>crease <strong>in</strong> ATPase activity could account for the abnormalities <strong>in</strong> these two conditions.<br />

Thallium cardiac scans (thallium‐210 SPECT scans) <strong>in</strong> patients with <strong>ME</strong>/CFS revealed moderate defects <strong>in</strong><br />

the left ventricle” (Arguments for a role of abnormal ionophore function <strong>in</strong> CFS. A Chaudhuri et al. In:<br />

Chronic Fatigue Syndrome. Ed: Yehuda and Mostofsky; Plenum Press, New York, 1997).<br />

1997<br />

“We report the prevalence of abnormal oscillat<strong>in</strong>g T waves at Holter monitor<strong>in</strong>g <strong>in</strong> a consecutive case series of<br />

<strong>ME</strong>/CFS patients from an <strong>in</strong>fectious diseases centre. Every <strong>ME</strong>/CFS patient, but only 22.4% of the non‐<strong>ME</strong>/CFS<br />

patients, showed abnormal oscillat<strong>in</strong>g T wave flatten<strong>in</strong>gs or <strong>in</strong>versions at Holter monitor<strong>in</strong>g. Abnormal<br />

cardiac wall motion at rest and stress, dilatation of the left ventricle, and segmental wall abnormalities<br />

were present. Left ventricular ejection fractions, at rest and with exercise, as low as 30% were seen <strong>in</strong><br />

<strong>ME</strong>/CFS patients. The abnormal (results) which we confirm here appear to be an essential element to the pathologic<br />

physiology of the cardiomyopathy of <strong>ME</strong>/CFS” (Cardiac Involvement <strong>in</strong> Patients with CFS as Documented with<br />

Holter and Biopsy Data <strong>in</strong> Michigan, 1991‐1993. AM Lerner et al. Infectious Diseases <strong>in</strong> Cl<strong>in</strong>ical Practice<br />

1997:6:327‐333).<br />

This research was summarised by Dr PD Corn<strong>in</strong>g, hav<strong>in</strong>g been reviewed and approved by Dr Lerner:

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

Saved successfully!

Ooh no, something went wrong!