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Effects of Conjugated Linoleic Acid and Metformin on Insulin Sensitivity in Obese Children: Randomized Clinical Trial
Author(s) -
Nayely Garibay-Nieto,
Gloria Eugenia Queipo-García,
Flor Ángel Ordóñez Álvarez,
Mayra Bustos,
Eréndira Villanueva-Ortega,
F.C Ramirez,
M. Piedra León,
Estibalitz LaresgoitiServitje,
Ravindranath Duggirala,
Teresa Macías,
Sergio Cuevas,
Abel Jalife,
Miguel A. Fonseca-Sánchez,
Fabiola Serratos,
Juan Carlos López-Alvarenga
Publication year - 2016
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jc.2016-2701
Subject(s) - insulin resistance , metformin , medicine , endocrinology , conjugated linoleic acid , homeostatic model assessment , insulin , placebo , glucose clamp technique , metabolic syndrome , type 2 diabetes , obesity , body mass index , diabetes mellitus , pancreatic hormone , linoleic acid , biology , fatty acid , biochemistry , alternative medicine , pathology
Context: Insulin resistance precedes metabolic syndrome abnormalities and may promote cardiovascular disease and type 2 diabetes in children with obesity. Results of lifestyle modification programs have been discouraging, and the use of adjuvant strategies has been necessary. Objective: This study aimed to evaluate the effects of metformin and conjugated linoleic acid (CLA) on insulin sensitivity, measured via euglycemic-hyperinsulinemic clamp technique and insulin pathway expression molecules in muscle biopsies of children with obesity. Design: A randomized, double-blinded, placebo-controlled clinical trial was conducted. Setting: Children with obesity were randomly assigned to receive metformin, CLA, or placebo. Results: Intervention had a positive effect in all groups. For insulin sensitivity Rd value (mg/kg/min), there was a statistically significant difference between the CLA vs placebo (6.53 ± 2.54 vs 5.05 ± 1.46, P = 0.035). Insulinemia and homeostatic model assessment of insulin resistance significantly improved in the CLA group (P = 0.045). After analysis of covariance was performed and the influence of body mass index, age, Tanner stage, prescribed diet, and fitness achievement was controlled, a clinically relevant effect size on insulin sensitivity remained evident in the CLA group (37%) and exceeded lifestyle program benefits. Moreover, upregulated expression of the insulin receptor substrate 2 was evident in muscle biopsies of the CLA group. Conclusions: Improvement of insulin sensitivity, measured via euglycemic-hyperinsulinemic clamp and IRS2 upregulation, favored patients treated with CLA.

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