Guest guest Posted April 12, 2012 Report Share Posted April 12, 2012 Dear Al Thanks for the heads-up on this. It's an area that has been under the spotlight several times. Unfortunately, as is usual, people who resort to patenting their findings often do so to obscure the factual content of their discoveries rather than to illuminate them. In this case, a (fairly superficial) search of USPTO records reveals nothing. How have they concealed it? It's not listed by any of the identifiers used in the article quoted below. Still, it's better to live in hope than die in despair. Regards R [CO-CURE] RES: Riordan Clinic Research Institute Has Developed and Patented a Process for the Assessment of the Energy Metabolism in Patients with Chronic Fatigue Syndrome. Date: Thu, 12 Apr 2012 07:49:48 -0500 From: kelly <kellylatta66@...> Reply-kelly <kellylatta66@...> CO-CURE@... Note: This is a public relations press release that was printed verbatim on the site. Press releases are specifically designed to follow a news format, in general, however rarely cite more than one source and do not present caveats such as adverse effects, cost etc. The study is not available through PubMed. Whether or not it would specifically assess post exertional malaise (PEM) which appears to differentiate ME and CFS patients from nearly all other medical patients with " fatigue " is unknown. Bio-medicine 4/11/2012 Riordan Clinic Research Institute Has Developed and Patented a Process for the Assessment of the Energy Metabolism in Patients with Chronic Fatigue Syndrome. WICHITA, Kan., April 11, 2012 /PRNewswire-USNewswire/ --Riordan Clinic scientists Dr. Nina Mikirova, Dr. ph Casciari, and Dr. Hunninghake have patented a new technology that may help doctors determine the severity of fatigue in their patients. The research, recently published in the January/February issue of the journal, Alternative Therapies, is entitled " The Assessment of the Energy Metabolism in Patients with Chronic Fatigue Syndrome by Serum Fluorescence Emission. " Chronic fatigue syndrome (CFS) is characterized by long-lasting disabling fatigue. It includes non-specific symptoms such as weakness, malaise, subjective fever, sore throat, lymph node pain, and decreased memory. There are no conclusive diagnostic tests for CFS. Since the underlying mechanism for CFS is not known, finding reliable biomarkers for diagnosing are important. The purpose of this study was to examine the use of serum nicotinamide adenine dinucleotide (NAD(P)H) levels as a metabolic marker of fatigue state and alterations in metabolism and homeostasis in CFS patients. The Riordan Clinic scientists have developed a method of determining NAD(P)H levels based on fluorescence emission of serum at 450 nm. Serum NAD(P)H concentrations were compared for subjects with CFS and healthy controls. NAD(P)H concentrations in the serum of CFS subjects averaged 8.0 +/- 1.4 (SD) uM while those in healthy controls averaged 10.8 +/- 0.8 (SD) uM, a statistically significant difference (p< 0.001). The sensitivity (detection of positives) and specificity (non-detection of negatives) of the test in matching CFS patients to control subjects at NAD(P)H cut-off of 9.5 uM were 0.73 and 0.98. The researchers also compared NAD(P)H concentrations to other endocrine and metabolic parameters. A factor analysis, based on the correlation matrix between all variables, demonstrated that the best correlations were between the NAD(P)H, serum coenzyme Q10 and urine pyrroles. As coenzyme Q10 is the component of a complex series of reactions that occur within mitochondria, the function of Q10 ultimately is linked to the generation of energy within the cells. The correlation between the lower level of coenzyme Q10 and lower NAD(P)H signals for patients with CFS suggests lower bioenergetics for these subjects. An inverse correlation was found between the level of serum emission and the level of pyrroles in urine. The pyrroles are often elevated in patients with mental illness. This molecule is well known for bio-toxicity and is associated with emotional stress. As a result of the study, researchers proposed that fatigue level and metabolic slowdown in CFS patients can be evaluated and monitored by serum NAD(P)H concentration measurements. The measurement of the fluorescence of reduced nicotinamide adenine dinucleotide in serum provides a non-invasive assay to estimate metabolism and fatigue levels in CFS patients. Following patient NAD(P)H levels over time may aid in selecting therapeutic strategies and monitoring treatment outcome. To read this and other articles written by Riordan Clinic researchers, go tohttp://www.riordanclinic.org/research/journal-articles.shtml. The Riordan Clinic is a progressive nutrition-based medical clinic located in Wichita, Kansas. For 36 years, the Riordan Clinic has integrated lifestyle and nutrition to help patients find the underlying causes of their illness. Since the inception in 1975, the mission has been clear and unwavering to " .stimulate an epidemic of health. " SOURCE Riordan Clinic Copyright©2010 PR Newswire. All rights reserved --------------------------------------------- Send posts toCO-CURE@... Unsubscribe athttp://www.co-cure.org/unsub.htm Select list topic options athttp://www.co-cure.org/topics.htm --------------------------------------------- Co-Cure's purpose is to provide information from across the spectrum of opinion concerning medical, research and political aspects of ME/CFS and/or FMS. We take no position on the validity of any specific scientific or political opinion expressed in Co-Cure posts, and we urge readers to research the various opinions available before assuming any one interpretation is definitive. The Co-Cure website<www.co-cure.org> has a link to our complete archive of posts as well as articles of central importance to the issues of our community. --------------------------------------------- Quote Link to comment Share on other sites More sharing options...
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