Lifestyle and metformin ameliorate insulin sensitivity independently of the genetic burden of established insulin resistance variants in Diabetes Prevention Program participants

Publication Description
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 if people with genetic enrichment for these IR-variants respond differently to interventions that aim to improve insulin sensitivity. We built a genetic risk score based on 17 established IR-variants and their 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 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 IR-GRS on change in ISI; higher IR-GRS was associated with 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 improved ISI, regardless of the genetic burden of IR-variants.

Primary Author
Hivert,M. F.
Christophi,C. A.
Franks,P. W.
Jablonski,K. A.
Ehrmann,D. A.
Kahn,S. E.
Horton,E. S.
Pollin,T. I.
Mather,K. J.
Perreault,L.
Barrett-Connor,E.
Knowler,W. C.
Florez,J. C.
Diabetes Prevention Program Research Group

Author Address
Department of Population Medicine, Harvard Pilgrim Health Care Institute, Harvard Medical School, Boston, Massachusetts Diabetes Research Center (Diabetes Unit), Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts Depar(TRUNCATED)

Volume
65

Issue
2

Start Page
520

Other Pages
6

Publisher
by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered

Author Address
Department of Population Medicine, Harvard Pilgrim Health Care Institute, Harvard Medical School, Boston, Massachusetts Diabetes Research Center (Diabetes Unit), Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts Depar(TRUNCATED)

URL
http://www.ncbi.nlm.nih.gov/pubmed/26525880?dopt=abstract

PMID
26525880

PMCID
PMC4747453



Reference Type
Journal Article

Periodical Full
Diabetes

Publication Year
2015

Publication Date
2-Nov

ISSN/ISBN
1939-327X

Document Object Index
10.2337/db15-0950

Accession Number
PMID: 26525880