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Homogeneity in the association of body mass index with type 2 diabetes across the UK Biobank : A Mendelian randomization study

Wainberg, Michael (författare)
Stanford Univ, Dept Comp Sci, Stanford, CA 94305 USA
Mahajan, Anubha (författare)
Univ Oxford, Wellcome Ctr Human Genet, Oxford, England;Univ Oxford, Oxford Ctr Diabet Endocrinol & Metab, Churchill Hosp, Oxford, England
Kundaje, Anshul (författare)
Stanford Univ, Dept Comp Sci, Stanford, CA 94305 USA
visa fler...
McCarthy, Mark I. (författare)
Univ Oxford, Wellcome Ctr Human Genet, Oxford, England;Univ Oxford, Oxford Ctr Diabet Endocrinol & Metab, Churchill Hosp, Oxford, England;Churchill Hosp, NIHR Oxford Biomed Res Ctr, Oxford, England;Genentech Inc, OMNI Human Genet, San Francisco, CA 94080 USA
Ingelsson, Erik, 1975- (författare)
Uppsala universitet,Science for Life Laboratory, SciLifeLab,Molekylär epidemiologi,Stanford Univ, Sch Med, Dept Med, Div Cardiovasc Med, Stanford, CA 94305 USA;Stanford Univ, Stanford Cardiovasc Inst, Stanford, CA 94305 USA
Sinnott-Armstrong, Nasa (författare)
Stanford Univ, Dept Genet, Stanford, CA 94305 USA
Rivas, Manuel A. (författare)
Stanford Univ, Dept Biomed Data Sci, Stanford, CA 94305 USA
visa färre...
 (creator_code:org_t)
2019-12-10
2019
Engelska.
Ingår i: PLoS Medicine. - : PUBLIC LIBRARY SCIENCE. - 1549-1277 .- 1549-1676. ; 16:12
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Background: Lifestyle interventions to reduce body mass index (BMI) are critical public health strategies for type 2 diabetes prevention. While weight loss interventions have shown demonstrable benefit for high-risk and prediabetic individuals, we aimed to determine whether the same benefits apply to those at lower risk.Methods and findings: We performed a multi-stratum Mendelian randomization study of the effect size of BMI on diabetes odds in 287,394 unrelated individuals of self-reported white British ancestry in the UK Biobank, who were recruited from across the United Kingdom from 2006 to 2010 when they were between the ages of 40 and 69 years. Individuals were stratified on the following diabetes risk factors: BMI, diabetes family history, and genome-wide diabetes polygenic risk score. The main outcome measure was the odds ratio of diabetes per 1-kg/m(2) BMI reduction, in the full cohort and in each stratum. Diabetes prevalence increased sharply with BMI, family history of diabetes, and genetic risk. Conversely, predicted risk reduction from weight loss was strikingly similar across BMI and genetic risk categories. Weight loss was predicted to substantially reduce diabetes odds even among lower-risk individuals: for instance, a 1-kg/m(2) BMI reduction was associated with a 1.37-fold reduction (95% CI 1.12-1.68) in diabetes odds among non-overweight individuals (BMI < 25 kg/m(2)) without a family history of diabetes, similar to that in obese individuals (BMI >= 30 kg/m(2)) with a family history (1.21-fold reduction, 95% CI 1.13-1.29). A key limitation of this analysis is that the BMI-altering DNA sequence polymorphisms it studies represent cumulative predisposition over an individual's entire lifetime, and may consequently incorrectly estimate the risk modification potential of weight loss interventions later in life.Conclusions In a population-scale cohort, lower BMI was consistently associated with reduced diabetes risk across BMI, family history, and genetic risk categories, suggesting all individuals can substantially reduce their diabetes risk through weight loss. Our results support the broad deployment of weight loss interventions to individuals at all levels of diabetes risk. 

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)

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