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骨保护素基因的A163G和G1181C多态性与骨质疏松症风险之间的显著关联,尤其是在绝经后女性中:一项荟萃分析。

Significant associations between the A163G and G1181C polymorphisms of the osteoprotegerin gene and risk of osteoporosis, especially in postmenopausal women: a meta-analysis.

作者信息

Luo Yi, Hu Zhenming, Hao Jie, Jiang Wei, Shen Jieliang, Zhao Jun

机构信息

Department of Orthopedic Surgery, The First Affiliated Hospital, Chongqing Medical University , Chongqing, China .

出版信息

Genet Test Mol Biomarkers. 2014 Mar;18(3):211-9. doi: 10.1089/gtmb.2013.0420. Epub 2014 Jan 10.

Abstract

OBJECTIVE

Whereas some studies have reported that the osteoprotegerin (OPG) gene is associated with osteoporosis risk in some studies, their results have proved inconclusive. We performed a meta-analysis of studies on the associations between OPG A163G and G1181C polymorphisms and the risk of osteoporosis.

METHODS

A literature search in PubMed, Embase, Web of Science, Cochrane Library, and China Biological Medicine (CBM) databases was conducted to identify all eligible case-control studies published before August 15th, 2013. Pooled odds ratios with their corresponding 95% confidence intervals were used to evaluate the strength of the association under either a fixed- or random-effect model according to the heterogeneity test.

RESULTS

Ten case-control studies were included with a total of 1673 osteoporosis cases and 1554 healthy controls in this meta-analysis. For the OPG A163G polymorphism, the combined results showed that the G allele of the A163G polymorphism may be associated with an increased risk of osteoporosis. Stratified analyses showed that the magnitude of the effect was similar among the Caucasian and postmenopausal women subgroups. Unlike the A163G polymorphism, the meta-analysis results revealed that the C allele of the G1181C polymorphism may be associated with a decreased risk of osteoporosis, especially in the Asian and postmenopausal women subgroups. No publication bias was detected for either polymorphism.

CONCLUSION

Our findings showed that the G allele of the OPG A163G polymorphism may increase osteoporosis risk, whereas the C allele of the G1181C polymorphism may protect individuals from osteoporosis. Both of these effects were observed in postmenopausal women.

摘要

目的

尽管一些研究报告称骨保护素(OPG)基因与骨质疏松症风险相关,但这些研究结果尚无定论。我们对OPG A163G和G1181C多态性与骨质疏松症风险之间关联的研究进行了荟萃分析。

方法

在PubMed、Embase、Web of Science、Cochrane图书馆和中国生物医学数据库(CBM)中进行文献检索,以识别2013年8月15日前发表的所有符合条件的病例对照研究。根据异质性检验,采用固定效应模型或随机效应模型,用合并比值比及其相应的95%置信区间来评估关联强度。

结果

本荟萃分析纳入了10项病例对照研究,共1673例骨质疏松症病例和1554例健康对照。对于OPG A163G多态性,综合结果表明,A163G多态性的G等位基因可能与骨质疏松症风险增加相关。分层分析表明,在白种人和绝经后女性亚组中,效应大小相似。与A163G多态性不同,荟萃分析结果显示,G1181C多态性的C等位基因可能与骨质疏松症风险降低相关,尤其是在亚洲和绝经后女性亚组中。两种多态性均未检测到发表偏倚。

结论

我们的研究结果表明,OPG A163G多态性的G等位基因可能增加骨质疏松症风险,而G1181C多态性的C等位基因可能使个体免受骨质疏松症影响。在绝经后女性中均观察到了这两种效应。

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