Lifestyle and Metformin Ameliorate Insulin Sensitivity Independently of the Genetic Burden of Established Insulin Resistance Variants in Diabetes Prevention Program Participants

被引:34
作者
Hivert, Marie-France [1 ,2 ,3 ]
Christophi, Costas A. [4 ]
Franks, Paul W. [5 ,6 ,7 ]
Jablonski, Kathleen A. [4 ]
Ehrmann, David A. [8 ]
Kahn, Steven E. [9 ,10 ]
Horton, Edward S. [11 ,12 ]
Pollin, Toni I. [13 ,14 ,15 ]
Mather, Kieren J. [16 ]
Perreault, Leigh [17 ]
Barrett-Connor, Elizabeth [18 ]
Knowler, William C. [19 ]
Florez, Jose C. [2 ,12 ,20 ,21 ]
机构
[1] Harvard Univ, Sch Med, Harvard Pilgrim Hlth Care Inst, Dept Populat Med, Boston, MA 02115 USA
[2] Massachusetts Gen Hosp, Dept Med, Diabet Res Ctr, Diabet Unit, Boston, MA 02114 USA
[3] Univ Sherbrooke, Dept Med, Sherbrooke, PQ J1K 2R1, Canada
[4] George Washington Univ, Ctr Biostat, Rockville, MD USA
[5] Lund Univ, Dept Clin Sci, Ctr Diabet, Genet & Mol Epidemiol Unit, Malmo, Sweden
[6] Harvard Univ, Sch Publ Hlth, Dept Nutr, 665 Huntington Ave, Boston, MA 02115 USA
[7] Umea Univ, Dept Publ Hlth & Clin Med, Div Med, Umea, Sweden
[8] Univ Chicago, Sch Med, Dept Med, Chicago, IL 60637 USA
[9] VA Puget Sound Hlth Care Syst, Div Metab Endocrinol & Nutr, Seattle, WA USA
[10] Univ Washington, Seattle, WA 98195 USA
[11] Joslin Diabet Ctr, Sect Clin Behav & Outcomes Res, Boston, MA 02215 USA
[12] Harvard Univ, Sch Med, Dept Med, Boston, MA 02115 USA
[13] Univ Maryland, Sch Med, Dept Med, Baltimore, MD 21201 USA
[14] Univ Maryland, Sch Med, Dept Epidemiol & Publ Hlth, Baltimore, MD 21201 USA
[15] Univ Maryland, Sch Med, Program Personalized & Genom Med, Baltimore, MD 21201 USA
[16] Indiana Univ Sch Med, Dept Med, Div Endocrinol, Indianapolis, IN 46202 USA
[17] Univ Colorado, Dept Med, Div Endocrinol Metab & Diabet, Anschutz Med Campus, Aurora, CO USA
[18] Univ Calif San Diego, Dept Family Med & Publ Hlth, Div Epidemiol, La Jolla, CA 92093 USA
[19] NIDDK, Diabet Epidemiol & Clin Res Sect, Phoenix, AZ USA
[20] Massachusetts Gen Hosp, Ctr Human Genet Res, Boston, MA 02114 USA
[21] Broad Inst, Program Med & Populat Genet, Cambridge, MA USA
基金
美国国家卫生研究院;
关键词
BETA-CELL DYSFUNCTION; RELATIVE CONTRIBUTIONS; GLUCOSE-TOLERANCE; GLYCEMIC TRAITS; INTERVENTION; HOMEOSTASIS; SECRETION;
D O I
10.2337/db15-0950
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Large genome-wide association studies of glycemic traits have identified genetics variants that are associated with insulin resistance (IR) in the general population. It is unknown whether people with genetic enrichment for these IR variants respond differently to interventions that aim to improve insulin sensitivity. We built a genetic risk score (GRS) based on 17 established IR variants and effect sizes (weighted IR-GRS) in 2,713 participants of the Diabetes Prevention Program (DPP) with genetic consent. We tested associations between the weighted IR-GRS and insulin sensitivity index (ISI) at baseline in all participants, and with change in ISI over 1 year of follow-up in the DPP intervention (metformin and lifestyle) and control (placebo) arms. All models were adjusted for age, sex, ethnicity, and waist circumference at baseline (plus baseline ISI for 1-year ISI change models). A higher IR-GRS was associated with lower baseline ISI (beta= -0.754 [SE = 0.229] log-ISI per unit, P = 0.001 in fully adjusted models). There was no differential effect of treatment for the association between the IR-GRS on the change in ISI; higher IR-GRS was associated with an attenuation in ISI improvement over 1 year (beta = -0.520 [SE = 0.233], P = 0.03 in fully adjusted models; all treatment arms). Lifestyle intervention and metformin treatment improved the ISI, regardless of the genetic burden of IR variants.
引用
收藏
页码:520 / 526
页数:7
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