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本文引用的文献

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The role of the factor V Leiden mutation in osteonecrosis of the hip.因子 V 莱顿突变在髋关节骨坏死中的作用。
Clin Appl Thromb Hemost. 2013 Sep;19(5):499-503. doi: 10.1177/1076029612449901. Epub 2012 Jun 12.
2
Role of factor V Leiden or G20210A prothrombin mutation in patients with symptomatic pulmonary embolism and deep vein thrombosis: a meta-analysis of the literature.凝血因子V莱顿突变或凝血酶原G20210A突变在有症状的肺栓塞和深静脉血栓形成患者中的作用:文献荟萃分析
J Thromb Haemost. 2012 Apr;10(4):732-7. doi: 10.1111/j.1538-7836.2012.04656.x.
3
Risk of myocardial infarction related to factor V Leiden mutation: a meta-analysis.与凝血因子V莱顿突变相关的心肌梗死风险:一项荟萃分析。
Genet Test Mol Biomarkers. 2010 Aug;14(4):493-8. doi: 10.1089/gtmb.2010.0017.
4
Thrombophilia, hypofibrinolysis, the eNOS T-786C polymorphism, and multifocal osteonecrosis.易栓症、纤维蛋白溶解功能减退、内皮型一氧化氮合酶T-786C多态性与多灶性骨坏死。
J Bone Joint Surg Am. 2008 Oct;90(10):2220-9. doi: 10.2106/JBJS.G.00616.
5
Genetic background of nontraumatic osteonecrosis of the femoral head in the Korean population.韩国人群非创伤性股骨头坏死的遗传背景。
Clin Orthop Relat Res. 2008 May;466(5):1041-6. doi: 10.1007/s11999-008-0147-1. Epub 2008 Mar 19.
6
Osteonecrosis of the femoral head: etiology, imaging and treatment.股骨头坏死:病因、影像学及治疗
Eur J Radiol. 2007 Jul;63(1):16-28. doi: 10.1016/j.ejrad.2007.03.019. Epub 2007 Jun 6.
7
Hyperhomocysteinemia and thrombosis: an overview.高同型半胱氨酸血症与血栓形成:综述
Arch Pathol Lab Med. 2007 Jun;131(6):872-84. doi: 10.5858/2007-131-872-HATAO.
8
Activated protein C resistance and factor V Leiden: a review.活化蛋白C抵抗与因子V Leiden:综述
Arch Pathol Lab Med. 2007 Jun;131(6):866-71. doi: 10.5858/2007-131-866-APCRAF.
9
Thrombophilia and avascular necrosis of femoral head in kidney allograft recipients.肾移植受者的血栓形成倾向与股骨头缺血性坏死
Nephrol Dial Transplant. 2006 Dec;21(12):3555-8. doi: 10.1093/ndt/gfl400. Epub 2006 Sep 12.
10
Pathophysiology and natural history of avascular necrosis of bone.骨缺血性坏死的病理生理学与自然史
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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.

DOI:10.3892/br.2013.93
PMID:24648992
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3917729/
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。