Variation at the Melanocortin 4 Receptor Gene and Response to Weight-Loss Interventions in the Diabetes Prevention Program

被引:28
作者
Pan, Qing [1 ]
Delahanty, Linda M. [2 ,3 ]
Jablonski, Kathleen A. [1 ]
Knowler, William C. [4 ]
Kahn, Steven E. [5 ,6 ]
Florez, Jose C. [3 ,7 ,8 ,9 ]
Franks, Paul W. [10 ,11 ,12 ]
机构
[1] George Washington Univ, Biostat Ctr, Dept Biostat & Epidemiol, Dept Stat, Rockville, MD USA
[2] Massachusetts Gen Hosp, Diabet Res Ctr, MGH Diabet Ctr, Dept Med, Boston, MA 02114 USA
[3] Harvard Univ, Sch Med, Dept Med, Boston, MA USA
[4] NIDDK, Diabet Epidemiol & Clin Res Sect, Phoenix, AZ USA
[5] VA Puget Sound Hlth Care Syst, Div Metab Endocrinol & Nutr, Seattle, WA USA
[6] Univ Washington, Seattle, WA 98195 USA
[7] Massachusetts Gen Hosp, Dept Med, Ctr Human Genet Res, Boston, MA 02114 USA
[8] Massachusetts Gen Hosp, Dept Med, Diabet Res Ctr, Diabet Unit, Boston, MA 02114 USA
[9] Broad Inst, Program Med & Populat Genet, Cambridge, MA USA
[10] Lund Univ, Dept Clin Sci, Malmo, Sweden
[11] Harvard Univ, Sch Publ Hlth, Dept Nutr, Boston, MA 02115 USA
[12] Umea Univ, Dept Publ Hlth & Clin Med, Umea, Sweden
基金
美国国家卫生研究院; 瑞典研究理事会;
关键词
LIFE-STYLE INTERVENTION; COMMON VARIANTS; MC4R GENE; OBESITY; RISK; MASS; ASSOCIATION; DEFICIENCY; METFORMIN; GROWTH;
D O I
10.1002/oby.20459
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To assess associations and genotype x treatment interactions for melanocortin 4 receptor (MC4R) locus variants and obesity-related traits. Design and Methods: Diabetes prevention program (DPP) participants (N = 3,819, of whom 3,356 were genotyped for baseline and 3,234 for longitudinal analyses) were randomized into intensive lifestyle modification (diet, exercise, weight loss), metformin or placebo control. Adiposity was assessed in a subgroup (n = 909) using computed tomography. All analyses were adjusted for age, sex, ethnicity and treatment. Results: The rs1943218 minor allele was nominally associated with short-term (6 month; P = 0.032) and long-term (2 year; P = 0.038) weight change. Eight SNPs modified response to treatment on short-term (rs17066856, rs9966412, rs17066859, rs8091237, rs17066866, rs7240064) or long-term (rs12970134, rs17066866) reduction in body weight, or diabetes incidence (rs17066829) (all P-interaction < 0.05). Conclusion: This is the first study to comprehensively assess the role of MC4R variants and weight regulation in a weight loss intervention trial. One MC4R variant was directly associated with obesity-related traits or diabetes; numerous other variants appear to influence body weight and diabetes risk by modifying the protective effects of the DPP interventions.
引用
收藏
页码:E520 / E526
页数:7
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