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bipolar disorder, big plump plumpers galleries com , omega3 fatty acids , st. john's wort, wiel, prostate, audience: doctors/health professionals, transfatty acids, macrobiotics, aging, saturated fat, coat problems, raw eggs, big plump , plump grannies , Based on the original questions that chronic inflammation we received from AHRQ and input from our TEPs, we addressed the following questions in this study: Diabetes What is the evidence in adults or chronic inflammation children with chronic inflammation a) type II diabetes, or b) insulin resistance/the metabolic syndrome for an effect of omega-3 fatty acids on: Total cholesterol. HDL cholesterol. LDL cholesterol. Triglycerides. What is the evidence in adults and children for an effect of omega-3 fatty acids on insulin sensitivity in a) type II diabetes, or b) the metabolic syndrome? Inflammatory Bowel Disease What is the evidence for the efficacy of omega-3 fatty acids in treatment of Crohn's disease and ulcerative colitis? What is the evidence in adults or children with inflammatory bowel disease that omega-3 fatty acids can replace steroids or other immunosuppressive drugs? What is the evidence that the benefits of omega-3 fatty acids are influenced by the concomitant administration of various immunosuppressive agents in the treatment of inflammatory bowel disease?
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In addition, omega-3 fatty acids may play an important role in brain development and function. Some evidence has suggested that omega-3 fatty big plump acids in the diet may protect against heart attack and stroke, as well as certain inflammatory diseases like arthritis, lupus, and asthma.1 The major dietary big plump sources of omega-3 fatty acids in the big plump U.S. population are fish, fish oil, vegetable oils (principally canola and soybean), walnuts, wheat germ, and some dietary supplements. Return to Contents Methods Key Questions We consulted with three technical expert panels (TEPs) on this project. The respective panels focused on the following conditions: Rheumatoid arthritis, systemic lupus erythematosis (SLE), and bone density/osteoporosis. Renal disease and diabetes. Gastrointestinal diseases. The TEPs advised us on refining the preliminary questions posed to us by AHRQ, determining the proper inclusion/exclusion criteria for the study and the populations of interest, establishing the proper outcomes measures, and conducting the appropriate analyses.
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