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雌激素受体基因多态性与人类性早熟的关联:一项系统评价和荟萃分析。

Association of estrogen receptor gene polymorphisms with human precocious puberty: a systematic review and meta-analysis.

作者信息

Luo Yan, Liu Qin, Lei Xun, Wen Yi, Yang Ya-Lan, Zhang Rui, Hu Meng-Yao

机构信息

a School of Public Health and Management, Research Center for Medicine and Social Development, Innovation Center for Social Risk Governance in Health, Chongqing Medical University , Chongqing , P.R. China.

出版信息

Gynecol Endocrinol. 2015 Jul;31(7):516-21. doi: 10.3109/09513590.2015.1031102. Epub 2015 Jun 2.

DOI:10.3109/09513590.2015.1031102
PMID:26036718
Abstract

This study aims to estimate the association between ESR1 polymorphisms (PvuII and XbaI) and ESR2 polymorphisms (RsaI and AluI) with precocious puberty. Relevant studies published before March 2014 were retrieved by a electronic search among nine databases. Meta-analysis of the pooled odds ratios (ORs) with 95% confidence intervals (CIs) was calculated. Four eligible case-control studies including 491 precocious puberty patients and 370 healthy controls were identified. Three studies reported ESR1 PvuII and XbaI polymorphism and one study reported ESR2 RsaI and AluI polymorphism. Increment of precocious puberty risk was associated with PvuII polymorphism in the heterosis model ((CT) versus TT: OR 1.42, 95% CI: 1.05-1.91, p = 0.02). Risk of precocious puberty was associated with XbaI polymorphism in the dominant model (GG + GA versus AA: OR 1.48, 95% CI: 1.11-1.97, p = 0.007) and the heterosis model (GA versus AA: OR 1.68, 95% CI: 1.23-2.29, p = 0.001). This meta-analysis suggests that ESR1 XbaI and PvuII polymorphisms are associated with precocious puberty susceptibility, and the relationship between ESR2 RsaI and AluI polymorphism with precocious puberty remains to be further investigated. Well-designed studies with large sample size among different polymorphisms and ethnicities are in urgent need to provide and update reliable data for comprehensive and definite conclusion.

摘要

本研究旨在评估雌激素受体1(ESR1)基因多态性(PvuII和XbaI)及雌激素受体2(ESR2)基因多态性(RsaI和AluI)与性早熟之间的关联。通过电子检索九个数据库,获取了2014年3月之前发表的相关研究。计算了合并优势比(OR)及95%置信区间(CI)的Meta分析。共纳入四项符合条件的病例对照研究,包括491例性早熟患者和370例健康对照。三项研究报道了ESR1的PvuII和XbaI多态性,一项研究报道了ESR2的RsaI和AluI多态性。在杂合子模型中,PvuII多态性与性早熟风险增加相关((CT) 对比TT:OR 1.42,95% CI:1.05 - 1.91,p = 0.02)。在显性模型(GG + GA对比AA:OR 1.48,95% CI:1.11 - 1.97,p = 0.007)和杂合子模型(GA对比AA:OR 1.68,95% CI:1.23 - 2.29,p = 0.001)中,XbaI多态性与性早熟风险相关。本Meta分析表明,ESR1的XbaI和PvuII多态性与性早熟易感性相关,ESR2的RsaI和AluI多态性与性早熟之间的关系仍有待进一步研究。迫切需要开展不同基因多态性和种族的大样本量、设计良好的研究,以提供和更新可靠的数据得出全面明确的结论。

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