Endocrine‐disrupting chemicals, risk of type 2 diabetes, and diabetes‐related metabolic traits: A systematic review and meta‐analysis

医学 2型糖尿病 邻苯二甲酸盐 二羟基化合物 置信区间 糖尿病 胰岛素抵抗 前瞻性队列研究 内科学 环境卫生 生理学 内分泌学 双酚A 化学 有机化学 环氧树脂
作者
Yan Song,Elizabeth L. Chou,Aileen Baecker,Nai‐Chieh Y. You,Yiqing Song,Qi Sun,Simin Liu
出处
期刊:Journal of Diabetes [Wiley]
卷期号:8 (4): 516-532 被引量:200
标识
DOI:10.1111/1753-0407.12325
摘要

Abstract Background Elevated blood or urinary concentrations of endocrine‐disrupting chemicals ( EDCs ) may be related to increased risk of type 2 diabetes ( T2D ). The aim of the present study was to assess the role of EDCs in affecting risk of T2D and related metabolic traits. Methods MEDLINE was searched for cross‐sectional and prospective studies published before 8 M arch 2014 into the association between EDCs (dioxin, polychlorinated biphenyl [ PCB ], chlorinated pesticide, bisphenol A [ BPA ], phthalate) and T2D and related metabolic traits. Three investigators independently extracted information on study design, participant characteristics, EDC types and concentrations, and association measures. Results Forty‐one cross‐sectional and eight prospective studies from ethnically diverse populations were included in the analysis. Serum concentrations of dioxins, PCBs , and chlorinated pesticides were significantly associated with T2D risk; comparing the highest to lowest concentration category, the pooled relative risks ( RR ) were 1.91 (95% confidence interval [ CI ] 1.44–2.54) for dioxins, 2.39 (95% CI 1.86–3.08) for total PCBs , and 2.30 (95% CI 1.81–2.93) for chlorinated pesticides. Urinary concentrations of BPA and phthalates were also associated with T2D risk; comparing the highest to lowest concentration categories, the pooled RR were 1.45 (95% CI 1.13–1.87) for BPA and 1.48 (95% CI 0.98–2.25) for phthalates. Further, EDC concentrations were associated with indicators of impaired fasting glucose and insulin resistance. Conclusions Persistent and non‐persistent EDCs may affect the risk of T2D . There is an urgent need for further investigation of EDCs , especially non‐persistent ones, and T2D risk in large prospective studies.
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