Department of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, Hefei, Anhui, China.
The Key Laboratory of Major Autoimmune Diseases, Anhui Medical University, Hefei, Anhui, China.
Horm Metab Res. 2018 Jun;50(6):469-477. doi: 10.1055/a-0620-8553. Epub 2018 Jun 8.
The associations between PvuII (T>C) and XbaI (A>G) polymorphisms of estrogen receptor alpha (ESR1) gene with type 2 diabetes mellitus (T2DM) or metabolic syndrome (MetS) are reported in many studies, but the results are inconsistent. This present work aims to assess the associations by performing a comprehensive meta-analysis. Relevant studies were searched through several databases. The pooled odd ratios (ORs) with 95% confidence intervals (CIs) were calculated to evaluate the associations of PvuII and XbaI polymorphisms with the risk of T2DM and MetS by using the STATA 14.0 software. Eight studies for T2DM and three articles about MetS were included in this meta-analysis. The overall results indicated that PvuII, rather than XbaI polymorphism, was associated with T2DM (regressive model: OR=0.673, 95% CI=0.550 to 0.823, p<0.001, p<0.003). The subgroup analysis based on race revealed an association of PvuII polymorphism with the decreased T2DM risk in Chinese population and a relationship between XbaI polymorphism and the reduced T2DM susceptibility in Caucasians. The difference of country may be one source of the heterogeneity for PvuII polymorphism and T2DM. However, neither PvuII nor XbaI polymorphism was related to the risk of MetS. The C allele of PvuII polymorphism presents a protective role in T2DM risk, especially in Chinese people. The G allele of XbaI polymorphism is related to a reduced risk for T2DM in Caucasian population. Nevertheless, neither of PvuII nor XbaI polymorphism is associated with MetS risk.
许多研究报告了雌激素受体α(ESR1)基因 PvuII(T>C)和 XbaI(A>G)多态性与 2 型糖尿病(T2DM)或代谢综合征(MetS)之间的关联,但结果不一致。本研究旨在通过进行综合荟萃分析来评估这些关联。通过多个数据库搜索相关研究。使用 STATA 14.0 软件计算合并的优势比(OR)及其 95%置信区间(CI),以评估 PvuII 和 XbaI 多态性与 T2DM 和 MetS 风险的关联。该荟萃分析纳入了 8 项关于 T2DM 的研究和 3 项关于 MetS 的文章。总体结果表明,PvuII 多态性而非 XbaI 多态性与 T2DM 相关(回归模型:OR=0.673,95%CI=0.550 至 0.823,p<0.001,p<0.003)。基于种族的亚组分析表明,PvuII 多态性与中国人 T2DM 风险降低相关,XbaI 多态性与白种人 T2DM 易感性降低相关。PvuII 多态性与 T2DM 之间的异质性可能源于国家的差异。然而,PvuII 或 XbaI 多态性均与 MetS 风险无关。PvuII 多态性的 C 等位基因在 T2DM 风险中表现出保护作用,尤其是在中国人群中。XbaI 多态性的 G 等位基因与白种人 T2DM 风险降低相关。然而,PvuII 或 XbaI 多态性均与 MetS 风险无关。
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