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| CHICAGO, Nov. 12 /PRNewswire/ via NewsEdge
Corporation -- New data presented to the Annual Meeting of the American
College of Allergy, Asthma and Immunology suggests the discovery of a
potential diagnostic tool and therapeutic measurement for CFS.
"Currently, the diagnosis of CFS involves a lengthy procedures of
eliminating other possible causes of severe fatigue lasting more than
six consecutive months," said Dr. Joseph Bellanti, M.D., and
Director of the International Center for Interdisciplinary Studies of Immunology at Georgetown University Medical Center, who identified a simple-to-test for urinary marker in CFS patients. The Centers for Disease Control and Prevention report that chronic fatigue symptoms affect more than 14 million people between the ages of 17-69 and in twice as many women as men. Last month a study published in the American Medical Association's The Archives of Internal Medicine reported that the incidence of CFS is significantly more prevalent than previous data suggests. The study reported women are 20 times more likely to develop CFS than breast cancer and more than 15 times more likely to contract CFS than lung cancer. CFS patients suffer a debilitating illness that drastically affects their ability to work and live normal lives. CFS patients are often unable to complete the simplest of tasks without being exhausted. "Dr. Bellanti's work may represent a major breakthrough that will help doctors provide earlier diagnosis and better treatment," said Dr. Georg Birkmayer, M.D., Ph.D., the researcher who first discovered the therapeutic application of NADH in cellular development and energy transmission. NADH is a naturally occurring coenzyme that activates bodily energy production. The Georgetown University Medical Center doctors'
groundbreaking CFS research involved the use of ENADA(R) NADH, a dietary
supplement. Results of an FDA approved, double-blind, placebo-controlled
cross-over study published in the February 1999 issue of Annals of
Allergy, Asthma and Immunology found that CFS patients taking ENADA, a
dietary supplement, were four times more likely to show improvements
compare to those taking a placebo. A follow-up open label study showed
72% of the patients taking ENADA achieved continued marked improvement
over time. After more than 18 months of using ENADA, more than 80% of
the CFS Dr. Bellanti is founder and director of Georgetown University Medical Center's International Center for Interdisciplinary Studies of Immunology. He is a professor of pediatrics and microbiology. Dr. Bellanti has served on the Maternal and Child health Study Section of the National institutes of Child Health and Human Development (NICHD) and the Allergy and Immunology Research Committee of the National Institute of Allergy and Infectious Diseases (NIAID). He has published more than 400 scientific papers, abstracts and books. He is the author of the widely renowned textbook on immunology, now in its third edition. ENADA is the only patented, stabilized, absorbable, oral form of NADH available. Additional information about the science and
research behind ENADA may be found on the company's website at
www.enada.com. Menuco Corporation's mission is to develop and market
safe, reliable and effective nutritional supplement products, which are
designed to improve the quality of life for all people. All of Menuco's
medical research is the result of a decade of research and extensive
toxicology and safety studies which were reviewed by the FDA,
culminating in the SOURCE |
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