Guest guest Posted March 7, 2011 Report Share Posted March 7, 2011 ** Looks like an essential fatty acid - essential to osteoarthritis sufferers at least - buy up if you can afford it would be my understanding - topically or orally some benefit found. In a review article - #8, the last one in this list found MSM to be more effective then CMO. I don't know how expensive the CMO is but MSM isn't too bad. 1. http://www.nutraingredients-usa.com/Research/Cetylated-fatty-acid-enables-osteoa\ rthritis-sufferers-to-exercise-shows-study Cetylated fatty acid enables osteoarthritis sufferers to exercise, shows study 2. http://www.nutraingredients-usa.com/Research/Science-The-emerging-ingredients-fo\ r-joint-health Science: The emerging ingredients for joint health, By ls, 20-Apr-2010 " New Jersey-based Proprietary Ingredients has also been building the science behind its cetylated fatty acid branded ingredient Celadrin. The ingredient has been reported to offer an alternative to NSAIDs when taken orally (J. Rheumatol. 2002, Vol. 29, pp. 1708-1712), and efficacy has also been reported for a topical application J. Rheumatol. 2004, Vol. 31, pp. 767-774). Results of a randomised clinical trial presented at the Scripps Integrated Medical Conference in San Diego in 2007 reported that the ingredient was effective at reducing knee pain in subjects with moderate osteoarthritis, compared with placebo. " 3. http://www.nutraingredients-usa.com/smartlead/view/273265/4/Biocell-Technology-L\ LC-Novel-Dietary-Ingredients EstraFlexâ„¢ CMO Esterfied Fatty Acid Carbons (EFAC) - A proprietary blend of cetylated fatty acids, including cetyl myristate, cetyl myristoleate, cetyl oleate, cetyl palmitoleate, and cetyl palmitate. 4. http://www.ncbi.nlm.nih.gov/pubmed/15088305 Effect of a cetylated fatty acid topical cream on functional mobility and quality of life of patients with osteoarthritis. 2004 article CONCLUSION: Use of a CFA topical cream is an effective treatment for improving knee ROM, ability to ascend/descend stairs, ability to rise from sitting, walk and sit down, and unilateral balance. 5. http://www.aafp.org/afp/2003/0115/p339.html 2003 article Alternative Therapies for Traditional Disease States: Osteoarthritis Am Fam Physician. 2003 Jan 15;67(2):339-344. Cetyl Myristoleate A new agent promoted for osteoarthritis treatment is cetyl myristoleate, a material synthesized from cetyl alcohol and myristoleic acid. The rationale for its use in osteoarthritis stems from the hypothesis that cetyl myristoleate may inhibit the cyclooxygenase and lipoxygenase pathways of arachidonic acid metabolism and, therefore, decrease production of pro-inflammatory prostaglandins and leukotrienes. 6. http://www.ncbi.nlm.nih.gov/pubmed/8207671 Diehl, HW, May EL, Cetyl myristoleate isolated from Swiss albino mice: an apparent protective agent against adjuvant arthritis in rats., J Pharm Sci. 1994 Mar;83(3):296-9. Abstract Cetyl myristoleate was isolated from National Institutes of Health, general purpose, Swiss albino mice that were immune to the polyarthritis induced in rats with Freund's adjuvant. This substance, or material synthesized from cetyl alcohol and myristoleic acid, afforded good protection against adjuvant-induced arthritic states in rats. In limited comparisons, cetyl oleate, also found in Swiss albino mice, gave lesser protection, whereas cetyl myristate and cetyl elaidate, the trans-isomer of cetyl oleate, appeared to be virtually ineffective. Dosage of the protective compound as well as the site of injection of Freund's adjuvant was important. 7. http://www.ncbi.nlm.nih.gov/pubmed/12526860 Hunter KW Jr, Gault RA, Stehouwer JS, Tam-Chang SW, Synthesis of cetyl myristoleate and evaluation of its therapeutic efficacy in a murine model of collagen-induced arthritis., Pharmacol Res. 2003 jan;47(1):43-7. Department of Microbiology, University of Nevada School of Medicine, Reno, NV 89557, USA. khunter@... Abstract Cetyl myristoleate (CM) was reported by Diehl and May [J Pharm Sci 83 (1994) 296] to block inflammation and prevent adjuvant-induced arthritis in rats. To verify this earlier work, we have synthesized pure CM and tested its anti-arthritic properties in a collagen-induced arthritis model in DBA/1LacJ mice. Multiple intraperitoneal injections of CM in 450 and 900 mg kg(-1) doses resulted in a significantly lower incidence of disease and caused a modest but significant diminution in clinical signs in those mice that developed arthritis. CM administered in daily oral doses of 20 mg kg(-1) also reduced the incidence of arthritis and caused a small reduction in the clinical signs in mice that developed arthritis. Although the protective effect of CM in collagen-induced arthritis observed in the present study was less dramatic than that reported earlier, our results confirm the anti-arthritic properties of pure CM. 8. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1779427/?tool=pubmed Osteoarthritis and nutrition. From nutraceuticals to functional foods: a systematic review of the scientific evidence t G Ameye and Winnie SS Chee free article - Table three compares the various things they reviewed. The oil cetyl myristoleate is the hexadecyl ester of the unsaturated fatty acid cis-9-tetradecenoic acid, commonly named myristoleic acid. Whereas myristoleic acid is commonly found in fish oils, whale oils, and dairy butter, cetyl myristoleate is known to exist only naturally in sperm whale oil and in a small gland in the male beaver. It can be synthesised by esterification of myristoleic acid. Although cetyl myristoleate is claimed to be beneficial for OA, there is lack of scientific evidence to support its efficacy. Nevertheless, a 68-day placebo-controlled single-blind RCT on severe knee OA (that is, LFI >14) concluded that three 500 mg capsules, containing 350 mg of a blend of olive oil and various cetylated fatty acids, 50 mg of lecithin, and 75 mg of fish oil, twice a day, significantly increased knee flexion compared with placebo [50] (Table 4). According to the best-evidence synthesis (Table 3), this low-quality RCT provides limited scientific evidence of efficacy for cetyl myristoleate. Hence, further research is needed to evaluate the safety and potential benefits of cetyl myristoleate and cetylated fatty acids in the treatment of OA. In summary, this review demonstrates that nutrition can improve the symptoms of declared OA. However, the role of nutrition in slowing down progression of the disease remains to be seen. The very few RCTs, which used structure-modifying variables as primary endpoints, were unable to demonstrate a benefit, but the area deserves further investigation. As a whole, nutritional research in OA is only in its infancy. Only a few ingredients have been tested, and research remains based mainly on a pharmacological type of approach (one molecule/one target) rather than on a nutritional, more holistic type of approach (multiple ingredients/multiple targets). The full potency of nutrition for patients with declared OA thus remains to be evaluated. In parallel, and except for a few longitudinal epidemiological studies on vitamins, no study has evaluated the value of nutrition in the prevention of OA. ** Nice summary, I don't see that kind of statement often. R Vajda, R.D. www.GingerJens.com ________________________________ To: rd-usa Sent: Mon, March 7, 2011 3:23:10 PM Subject: cetyl myristoleate (CMO) I am looking for input on a supplement called Cetyl Myristoleate (CMO) that my brother started taking for his knees that are in constant pain from numerous surgeries, he was told by a physical therapist where he lives i n MD about this and he said he has had immediate and almost complete relief from pain, I am going to check with the Natural Database online reference, but wondered if anyone has had any experience with it. My daughter has inherited the bad knees, and I have degenerative disc disease in my spine that hasn't responded to much, was wondering about possibility of it helping both of us also, I am cautious about taking things without some reading into it. thanks in advance. Sue Nichols NOTICE: This confidential message/attachment contains information intended for a specific individual(s) and purpose. Any inappropriate use, distribution or copying is strictly prohibited. If received in error, please notify the sender and immediately delete the message. Thank you. Sue Nichols, MS/RD/CDE/CDN Quote Link to comment Share on other sites More sharing options...
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