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因子V莱顿突变:黎巴嫩患者静脉血栓形成的常见风险因素。

Factor V-Leiden Mutation: A Common Risk Factor for Venous Thrombosis among Lebanese Patients.

作者信息

Kreidy Raghid

机构信息

Department of Vascular Surgery, Saint George Hospital, University Medical Center, University of Balamand, P.O. Box 166378, Achrafieh, Beirut 1100 2807, Lebanon.

出版信息

Thrombosis. 2012;2012:380681. doi: 10.1155/2012/380681. Epub 2012 Jun 12.

Abstract

Aim. Lebanon exhibits one of the highest prevalences of factor V-Leiden (FVL) in the world (14.4%). The aim of this study is to evaluate the incidence of FVL mutation among Lebanese patients with lower extremity venous thrombosis. Material and Methods. From January 2003 to January 2011, 283 consecutive Lebanese patients, diagnosed with deep venous thrombosis (DVT) by duplex scan, were retrospectively reviewed. FVL mutation was tested among patients with conditions highly suggestive of hypercoagulation states (65 patients). Results. FVL mutation was detected among 56.9% of patients, 68.6% of patients younger than 50 years, and 43.4% of patients older than 50 years (P = 0.041). FVL mutation was commonly reported in young adults, in patients with pregnancy, estrogen drugs, recurrent DVT, and resistance to anticoagulation. Conclusion. The high rate of FVL mutation observed among Lebanese patients with venous thrombosis is related to the high prevalence of this mutation in the Lebanese population. Thrombophilia screening should be tailored to accommodate a population's risk factor. In countries with high prevalence of FVL, this mutation should be screened among patients younger than 50 years and patients with situations highly suggestive of hypercoagulation states.

摘要

目的。黎巴嫩是世界上因子V莱顿(FVL)患病率最高的国家之一(14.4%)。本研究的目的是评估黎巴嫩下肢静脉血栓形成患者中FVL突变的发生率。材料与方法。回顾性分析2003年1月至2011年1月期间连续收治的283例经双功扫描诊断为深静脉血栓形成(DVT)的黎巴嫩患者。对高度怀疑存在高凝状态的患者(65例)进行FVL突变检测。结果。在56.9%的患者中检测到FVL突变,50岁以下患者中为68.6%,50岁以上患者中为43.4%(P = 0.041)。FVL突变常见于年轻成年人、妊娠患者、使用雌激素药物患者、复发性DVT患者以及对抗凝治疗有抵抗的患者。结论。黎巴嫩静脉血栓形成患者中观察到的FVL突变高发生率与该突变在黎巴嫩人群中的高患病率有关。血栓形成倾向筛查应根据人群的危险因素进行调整。在FVL患病率高的国家,应在50岁以下患者以及高度怀疑存在高凝状态的患者中进行该突变的筛查。

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