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凝血因子V Leiden基因G1691A多态性与股骨头坏死易感性的Meta分析。

Meta-analysis of Factor V Leiden G1691A polymorphism and osteonecrosis of femoral head susceptibility.

作者信息

Shang Xifu, Luo Zhengliang, Li Xu, Hu Fei, Zhao Qichun, Zhang Wenzhi

机构信息

Department of Orthopedic Surgery, Anhui Provincial Hospital Affiliated to Anhui Medical University, Hefei, Anhui 230001, P.R. China.

出版信息

Biomed Rep. 2013 Jul;1(4):594-598. doi: 10.3892/br.2013.93. Epub 2013 Apr 9.

Abstract

Testing for genetic risk associations between Factor V Leiden (FVL) and the osteonecrosis of femoral head (ONFH) is common, however, inconsistent results have been previously obtained. To summarize results on the association of FVL mutation polymorphism with ONFH in various populations and to calculate the overall genetic risk factors, we performed a search of electronic databases including PubMed, Elsevier Science Direct, Chinese National Knowledge Infrastructure and the Chinese Biomedical Database to identify published studies correlating the FVL mutation with ONFH. Statistical analysis was performed using Review Manager (RevMan) version 5.0 and Stata statistical software (version 10). We identified 57 titles and included 7 studies comprising 481 cases and 867 controls in this meta-analysis. The groups were pooled, and a significant association between FVL mutation and increased ONFH was found (OR=4.55, 95% CI, 2.75-7.52, P<0.00001). This meta-analysis demonstrated that FVL plays an important role in non-Asian populations. Large sample studies including different ethnic groups and age- and gender-matched groups, as well as multiple gene polymorphism detection should be considered to clarify the association of FVL mutation polymorphism and ONFH susceptibility in the future.

摘要

检测凝血因子V莱顿突变(FVL)与股骨头坏死(ONFH)之间的遗传风险关联很常见,然而,此前已得到不一致的结果。为总结不同人群中FVL突变多态性与ONFH关联的结果并计算总体遗传风险因素,我们检索了包括PubMed、爱思唯尔科学直达、中国知网和中国生物医学数据库在内的电子数据库,以识别已发表的将FVL突变与ONFH相关联的研究。使用Review Manager(RevMan)5.0版和Stata统计软件(10版)进行统计分析。我们在这项荟萃分析中识别出57个标题,并纳入了7项研究,包括481例病例和867例对照。对各研究组进行合并后,发现FVL突变与ONFH增加之间存在显著关联(OR = 4.55,95% CI,2.75 - 7.52,P < 0.00001)。这项荟萃分析表明,FVL在非亚洲人群中起重要作用。未来应考虑开展包括不同种族以及年龄和性别匹配组的大样本研究,以及多基因多态性检测,以阐明FVL突变多态性与ONFH易感性之间的关联。

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