TY - JOUR
T1 - Diabetes genetic risk score modifies effect of bisphenol a exposure on deterioration in glucose metabolism
AU - Bi, Yufang
AU - Wang, Weiqing
AU - Xu, Min
AU - Wang, Tiange
AU - Lu, Jieli
AU - Xu, Yu
AU - Dai, Meng
AU - Chen, Yuhong
AU - Zhang, Di
AU - Sun, Wanwan
AU - Ding, Lin
AU - Chen, Ying
AU - Huang, Xiaolin
AU - Lin, Lin
AU - Qi, Lu
AU - Lai, Shenghan
AU - Ning, Guang
N1 - Publisher Copyright:
Copyright © 2016 by the Endocrine Society.
PY - 2016/1
Y1 - 2016/1
N2 - Context: Epidemiology studies showed inconsistent results regarding the relationship between bisphenol A (BPA) exposure and risk of type 2 diabetes (T2D). Objective: This study sought to prospectively investigate associations of BPA with incident T2D risk and the longitudinal changes in glycemic traits, particularly examining the interaction between gene and BPA exposure on the associations. Design, Setting, and Participants: A community-based study was conducted at baseline in 2009, including 2209 nondiabetic middle-age and elderly subjects followed for 4 y. Urinary BPA levels were measured at baseline. A genetic risk score (GRS) based on 34 T2D common variants that identified and validated in East Asians was created. Main Outcome Measures: Incident T2D was defined according to the 1999 World Health Organization criteria. Fasting (FPG) and 2-h post-loading plasma glucose were measured at baseline and followup. Results: Multivariable logistic regression analysis demonstrated no significant association of risk of incident T2D with BPA while with increase in the weighted T2D-GRS (odds ratio, 1.89; 95% confidence interval, 1.31â€"2.72 for each 10-point increment). Similar results were found in 4-y changes of FPG and 2-h post-loading plasma glucose. The GRS modified the effect of BPA exposure on 4-y changes in FPG (P for interaction = .01). Each 1 unit of Log-BPA was associated with 0.1 mmol/L increase in FPG (P = .007) in the highest quartile of GRS; no associations were found in the lower three quartiles of GRS. Conclusions: The T2D genetic susceptibility significantly modulated the association of BPA exposure with longitudinal increase in FPG levels.
AB - Context: Epidemiology studies showed inconsistent results regarding the relationship between bisphenol A (BPA) exposure and risk of type 2 diabetes (T2D). Objective: This study sought to prospectively investigate associations of BPA with incident T2D risk and the longitudinal changes in glycemic traits, particularly examining the interaction between gene and BPA exposure on the associations. Design, Setting, and Participants: A community-based study was conducted at baseline in 2009, including 2209 nondiabetic middle-age and elderly subjects followed for 4 y. Urinary BPA levels were measured at baseline. A genetic risk score (GRS) based on 34 T2D common variants that identified and validated in East Asians was created. Main Outcome Measures: Incident T2D was defined according to the 1999 World Health Organization criteria. Fasting (FPG) and 2-h post-loading plasma glucose were measured at baseline and followup. Results: Multivariable logistic regression analysis demonstrated no significant association of risk of incident T2D with BPA while with increase in the weighted T2D-GRS (odds ratio, 1.89; 95% confidence interval, 1.31â€"2.72 for each 10-point increment). Similar results were found in 4-y changes of FPG and 2-h post-loading plasma glucose. The GRS modified the effect of BPA exposure on 4-y changes in FPG (P for interaction = .01). Each 1 unit of Log-BPA was associated with 0.1 mmol/L increase in FPG (P = .007) in the highest quartile of GRS; no associations were found in the lower three quartiles of GRS. Conclusions: The T2D genetic susceptibility significantly modulated the association of BPA exposure with longitudinal increase in FPG levels.
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U2 - 10.1210/jc.2015-3039
DO - 10.1210/jc.2015-3039
M3 - Article
C2 - 26523527
AN - SCOPUS:84954494508
SN - 0021-972X
VL - 101
SP - 143
EP - 150
JO - Journal of Clinical Endocrinology and Metabolism
JF - Journal of Clinical Endocrinology and Metabolism
IS - 1
ER -