Suppr超能文献

儿茶酚-O-甲基转移酶158G/A和细胞色素P450 1B1 432C/G基因多态性增加子宫内膜异位症和子宫腺肌病的风险:一项荟萃分析。

COMT 158G/A and CYP1B1 432C/G polymorphisms increase the risk of endometriosis and adenomyosis: a meta-analysis.

作者信息

Tong Xiang, Li Zhenzhen, Wu Yao, Fu Xiaowei, Zhang Yonggang, Fan Hong

机构信息

West China School of Medicine/West China Hospital, Sichuan University, Chengdu, Sichuan, China.

The Periodical Press of West China Hospital, Sichuan University, Chengdu, Sichuan, China.

出版信息

Eur J Obstet Gynecol Reprod Biol. 2014 Aug;179:17-21. doi: 10.1016/j.ejogrb.2014.04.039. Epub 2014 May 13.

Abstract

OBJECTIVE

Catechol-O-methyltransferase (COMT) 158G/A and cytochrome P450-1B1 (CYP1B1) 432C/G gene polymorphisms have been associated with the risk of endometriosis and adenomyosis, but results remain inconclusive. The aim of this study was to investigate the relationships between these polymorphisms and the risk of endometriosis and adenomyosis by meta-analysis.

STUDY DESIGN

A search was performed using PubMed, Embase, the Chinese Journals Full-text Database and Wanfang databases up to September 2013. Odds ratios (OR) and 95% confidence intervals (95% CI) were used to evaluate the relationships. Statistical analyses were undertaken using STATA Version 11.0.

RESULTS

The literature search identified 10 articles, involving 1770 cases and 2057 controls. The two polymorphisms were found to be significantly associated with the risk of endometriosis and adenomyosis (COMT 158 G/A: AA+AG vs GG: OR 1.20, 95% CI 1.01-1.43; CYP1B1 432 C/G: GG+GC vs CC: OR 1.28, 95% CI 1.01-1.68). In the subgroup analysis by ethnicity, the two polymorphisms were significantly associated with the risk of endometriosis and adenomyosis among Asian populations but not among Caucasian populations.

CONCLUSIONS

COMT 158G/A and CYP1B1 432C/G polymorphisms may contribute to the risk of endometriosis and adenomyosis, particularly in Asian populations. Larger studies are required to evaluate this association further.

摘要

目的

儿茶酚-O-甲基转移酶(COMT)158G/A和细胞色素P450-1B1(CYP1B1)432C/G基因多态性与子宫内膜异位症和子宫腺肌病的风险相关,但结果仍无定论。本研究的目的是通过荟萃分析探讨这些多态性与子宫内膜异位症和子宫腺肌病风险之间的关系。

研究设计

截至2013年9月,使用PubMed、Embase、中国期刊全文数据库和万方数据库进行检索。采用优势比(OR)和95%置信区间(95%CI)来评估关系。使用STATA 11.0版进行统计分析。

结果

文献检索共纳入10篇文章,涉及1770例病例和2057例对照。发现这两种多态性与子宫内膜异位症和子宫腺肌病的风险显著相关(COMT 158 G/A:AA + AG与GG相比:OR 1.20,95%CI 1.01 - 1.43;CYP1B1 432 C/G:GG + GC与CC相比:OR 1.28,95%CI 1.01 - 1.68)。在按种族进行的亚组分析中,这两种多态性与亚洲人群中子宫内膜异位症和子宫腺肌病的风险显著相关,但在白种人群中则不然。

结论

COMT 158G/A和CYP1B1 432C/G多态性可能会增加子宫内膜异位症和子宫腺肌病的风险,尤其是在亚洲人群中。需要开展更大规模的研究来进一步评估这种关联。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验