Association of estrogen receptor gene polymorphisms with human precocious puberty: a systematic review and meta-analysis. (3rd July 2015)

• Record Type: Journal Article
• Authors: Luo, Yan; Liu, Qin; Lei, Xun; Wen, Yi; Yang, Ya-Lan; Zhang, Rui; Hu, Meng-Yao
• Is Part Of: Gynecological endocrinology. Volume 31:Number 7(2015:Jul.)
• Page Start: 516
• Page End: 521
• Publication Date: 2015-07-03
• Subjects: Estrogen receptor -- meta-analysis -- polymorphism -- precocious puberty -- systematic review; Endocrine gynecology -- Periodicals; Generative organs, Female -- Diseases -- Periodicals; 618.1
• DOI: 10.3109/09513590.2015.1031102
• Languages: English
• ISSNs: 0951-3590

Abstract

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.