Genetic susceptibility to diabetes and long-term improvement of insulin resistance and β cell function during weight loss: the Preventing Overweight Using Novel Dietary Strategies (POUNDS LOST) trial

被引:33
作者
Huang, Tao [1 ,2 ,3 ]
Ley, Sylvia H. [4 ]
Zheng, Yan [4 ]
Wang, Tiange [1 ,4 ]
Bray, George A. [5 ]
Sacks, Frank M. [4 ]
Qi, Lu [1 ,4 ,6 ,7 ]
机构
[1] Tulane Univ, Sch Publ Hlth & Trop Med, Dept Epidemiol, New Orleans, LA 70118 USA
[2] Natl Univ Singapore, Saw Swee Hock Sch Publ Hlth, Epidemiol Domain, Singapore, Singapore
[3] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Med, Singapore, Singapore
[4] Harvard TH Chan Sch Publ Hlth, Dept Nutr, Boston, MA USA
[5] Louisiana State Univ Syst, Pennington Biomed Res Ctr, Baton Rouge, LA USA
[6] Brigham & Womens Hosp, Dept Med, Channing Div Network Med, 75 Francis St, Boston, MA 02115 USA
[7] Harvard Med Sch, Boston, MA USA
基金
中国国家自然科学基金;
关键词
genetic risk score; weight-loss diets; insulin resistance; beta cell function; gene-diet interaction; PROTEIN-INTAKE; GLUCOSE-METABOLISM; TYPE-2; ASSOCIATION; CARBOHYDRATE; ARCHITECTURE; POPULATIONS; PREDISPOSITION; INSIGHT; TRAITS;
D O I
10.3945/ajcn.115.121186
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: Diet interventions have shown effectiveness in improving diabetes risk factors; however, little is known about whether the effects of diet intervention are different according to genetic susceptibility. Objective: We examined interactions between weight-loss diets and the genetic risk score (GRS) for diabetes on 2-y changes in markers of insulin resistance and beta cell function in a randomized controlled trial. Design: Data from the Preventing Overweight Using Novel Dietary Strategies (POUNDS LOST) trial were analyzed. A GRS was calculated on the basis of 31 diabetes-associated variants in 744 overweight or obese nondiabetic adults (80% white Americans). We assessed the changes in insulin resistance and beta cell function over the 2-y intervention. Results: Dietary protein significantly interacted with the diabetes GRS on fasting insulin, glycated hemoglobin (HbA1c), the homeostasis model assessment of beta cell function (HOMA-B), and the homeostasis model assessment of insulin resistance (HOMA-IR) at 2 y in white Americans (P-interaction = 0.02, 0.04, 0.01, and 0.05, respectively). The lower GRS was associated with a greater decrease in fasting insulin (P = 0.04), HbA1c (P = 0.0001), and HOMA-IR (P = 0.02), and a lesser increase in HOMA-B (P = 0.004) in participants consuming a low-protein diet. Participants with a higher GRS might have a greater reduction in fasting insulin when consuming a high-protein diet (P = 0.03). Conclusions: Our data suggest that individuals with a lower genetic risk of diabetes may benefit more from consuming a low-protein weight-loss diet in improving insulin resistance and beta cell function, whereas a high-protein diet may be more beneficial for white patients with a higher genetic risk.
引用
收藏
页码:198 / 204
页数:7
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