Arsov Todor, Miladinova Daniela, Spiroski Mirko
Laboratory of Molecular Diagnostics, Department of Hematology, University Hospital and Faculty of Medicine in Skopje, Republic of Macedonia.
Croat Med J. 2006 Jun;47(3):433-9.
To determine the prevalence of factor V Leiden mutation in patients with different presentation of venous thromboembolic disease and healthy individuals in the Republic of Macedonia.
The retrospective case control study involved 190 patients with venous thromboembolic disease and 200 healthy individuals, who were screened for the presence of factor V Leiden mutation, using a polymerase chain reaction-restriction fragment length polymorphism method. The prevalence of factor V Leiden was analyzed according to the localization of thrombosis, presence of risk factors, and family history of thrombosis. The odds of deep venous thrombosis were calculated with respect to the presence of factor V Leiden mutation.
The prevalence of factor V Leiden mutation among patients with venous thromboembolic disease was 21.1%, compared with 5.5% in the healthy individuals. Factor V Leiden positive patients had the first episode of deep venous thrombosis at a younger age, and the prevalence of the mutation was the highest among patients with a positive family history of thrombosis (33.9%, P=0.003) and in patients with deep venous thrombosis affecting a large blood vessel (37.7%, P=0.001). The prevalence of factor V Leiden mutation was lower in patients with calf deep venous thrombosis and primary thromboembolism (13.3% and 13.1%, respectively; P>0.05). The odds ratio for iliofemoral or femoral deep venous thrombosis in factor V Leiden carriers was 10.4 (95% confidence interval, 4.7-23.1).
The prevalence of factor V Leiden mutation was high in patients with venous thromboembolic disease and healthy individuals in the Republic of Macedonia. Factor V Leiden carriers have the highest odds of developing deep venous thrombosis affecting a large venous blood vessel.
确定马其顿共和国不同表现形式的静脉血栓栓塞性疾病患者及健康个体中凝血因子V莱顿突变的患病率。
这项回顾性病例对照研究纳入了190例静脉血栓栓塞性疾病患者和200名健康个体,采用聚合酶链反应-限制性片段长度多态性方法筛查凝血因子V莱顿突变的存在情况。根据血栓形成的部位、危险因素的存在情况以及血栓形成的家族史分析凝血因子V莱顿的患病率。计算凝血因子V莱顿突变携带者发生深静脉血栓形成的比值比。
静脉血栓栓塞性疾病患者中凝血因子V莱顿突变的患病率为21.1%,而健康个体中为5.5%。凝血因子V莱顿阳性的患者首次发生深静脉血栓形成的年龄较轻,且在有血栓形成家族史阳性的患者中该突变的患病率最高(33.9%,P = 0.003),在累及大血管的深静脉血栓形成患者中也最高(37.7%,P = 0.001)。在小腿深静脉血栓形成和原发性血栓栓塞患者中凝血因子V莱顿突变的患病率较低(分别为13.3%和13.1%;P>0.05)。凝血因子V莱顿携带者发生髂股或股深静脉血栓形成的比值比为10.4(95%置信区间,4.7 - 23.1)。
马其顿共和国静脉血栓栓塞性疾病患者及健康个体中凝血因子V莱顿突变的患病率较高。凝血因子V莱顿携带者发生累及大静脉血管的深静脉血栓形成的几率最高。