AI Article Synopsis

  • - This study explored the effects of conjugated linoleic acid (CLA) supplementation, with and without Vitamin E, on various health indicators in patients with type 2 diabetes over 8 weeks.
  • - A total of 56 participants were randomly assigned to three groups: CLA + Vitamin E, CLA + placebo, and placebo + Vitamin E, with their body composition and metabolic markers measured before and after the trial.
  • - Results indicated no significant differences in health indicators among the groups after the 8 weeks, suggesting that CLA supplementation does not improve metabolic control in overweight patients with type 2 diabetes.

Article Abstract

Background: The healthy properties of conjugated linoleic acid (CLA) such as weight loss, reducing cardiovascular risk factors and inflammation have been reported. The trans-10, cis-12 CLA isomer is related to increasing insulin resistance, but the effects of cis-9, trans-11 isomer is not clear. The aim of this study was to investigate the effects of CLA with and without Vitamin E on body weight, body composition, glycemic index, inflammatory and coagulation factors, lipid profile, serum leptin and adiponectin, malondialdehyde (MDA), and blood pressure in type2 diabetes.

Methods: 56 patients with type2 diabetes were included in 8 week double-blind control trial that used metformin. They randomly divided into three groups: CLA + VitE, CLA + VitE placebo, CLA placebo + VitE placebo. All variables, anthropometric measurements, and body composition were evaluated at the beginning and the end of study. Statistical analysis and analysis of dietary data were performed using SPSS and nutritionist IV software, respectively.

Results: There were not any significant differences in variable changes among three groups. However, there was a trend to increase in MDA and decrease in apoB100 among CLA consumers.

Conclusion: The results of this study showed that administration of CLA supplementation for 8 weeks does not affect any indicators of metabolic control in overweight type2 diabetic patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7976596PMC
http://dx.doi.org/10.1186/2251-6581-12-42DOI Listing

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