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Effect of glutamine supplementation on cardiovascular risk factors in patients with type 2 diabetes

Abstract Objective The aim of this study was to assess clinical relevance of long-term oral glutamine supplementation on lipid profile and inflammatory and metabolic factors in patients with diabetes. Method Sixty-six patients with type 2 diabetes between the ages of 18 and 65 y were randomized to r...

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Published in:Nutrition (Burbank, Los Angeles County, Calif.) Los Angeles County, Calif.), 2015, Vol.31 (1), p.119-126
Main Authors: Mansour, Asieh, M.Sc, Mohajeri- Tehrani, Mohammad Reza, M.D, Qorbani, Mostafa, Ph.D, Heshmat, Ramin, M.D., Ph.D, Larijani, Bagher, M.D, Hosseini, Saeed, M.D., Ph.D
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Language:English
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Summary:Abstract Objective The aim of this study was to assess clinical relevance of long-term oral glutamine supplementation on lipid profile and inflammatory and metabolic factors in patients with diabetes. Method Sixty-six patients with type 2 diabetes between the ages of 18 and 65 y were randomized to receive glutamine 30 g/d (10 g powder, three times a day) or placebo, in a double-blind, placebo-controlled trial during a 6-wk treatment period. Fifty-three patients completed the trial. Independent samples t  test and analysis of covariance were used. Results After a 6-wk treatment period, a significant difference was observed between the two groups in body fat mass ( P  = 0.01) and percentage of body fat ( P  = 0.008). Moreover, a significant reduction in waist circumference ( P   0.05). No significant difference was observed between groups in total cholesterol, high-density lipoprotein cholesterol, low-density lipoprotein cholesterol and triglyceride. No treatment effect on C-reactive protein was found ( P  = 0.44). Conclusion We demonstrated that the 6-wk supplementation with 30 g/d glutamine markedly improved some cardiovascular risk factors, as well as body composition, in patients with type 2 diabetes. Future glutamine dose–response studies are warranted in these areas.
ISSN:0899-9007
1873-1244
DOI:10.1016/j.nut.2014.05.014