Turkstra F, Karemaker R, Kuijer P M, Prins M H, Büller H R
Center for Haemostasis, Thrombosis, Artherosclerosis and Inflammation Research, Academic Medical Center, University of Amsterdam, The Netherlands.
Thromb Haemost. 1999 Mar;81(3):345-8.
Previous investigations have suggested a lower prevalence of the factor V Leiden mutation in patients with pulmonary embolism, as compared to patients with deep leg vein thrombosis.
We studied unselected patients with pulmonary embolism, in whom we also assessed the presence of deep vein thrombosis by ultrasonography. We assessed the prevalence of heterozygosity for the factor V Leiden mutation and compared the outcome of patients with a normal ultrasound (primary pulmonary embolism) to those with an abnormal ultrasound (combined form of venous thromboembolism). Furthermore, we performed a literature search to identify all articles regarding the prevalence of heterozygous factor V Leiden mutation in patients with primary deep vein thrombosis, primary pulmonary embolism and a combined form of venous thromboembolism. We calculated a (common) odds ratio for these 3 manifestations of venous thromboembolism, including the current findings.
In 92 patients with proven pulmonary embolism, 25 (27%) had also an abnormal ultrasound. In these patients, the prevalence of the factor V Leiden mutation was 24% (95% CI 9%-45%), whereas the mutation was present in 5 of 67 patients with primary pulmonary embolism (7%; 95% CI 2%-16%). The literature analysis indicated the common odds ratio for the presence of heterozygous factor V Leiden mutation in patients with primary deep vein thrombosis, primary pulmonary embolism and the combined form of venous thromboembolism to be 7.9 (95% CI 5-12), 3.5 (95% CI 2-6) and 6.8 (95% CI 3-14), respectively.
In patients with primary pulmonary embolism the prevalence of the factor V Leiden mutation appears to be half of that reported in patients with primary deep vein thrombosis. The mechanism remains unclear.
先前的研究表明,与下肢深静脉血栓形成患者相比,肺栓塞患者中因子V莱顿突变的发生率较低。
我们研究了未经挑选的肺栓塞患者,通过超声检查评估他们是否存在深静脉血栓形成。我们评估了因子V莱顿突变杂合子的发生率,并将超声检查正常的患者(原发性肺栓塞)与超声检查异常的患者(静脉血栓栓塞的联合形式)的结果进行比较。此外,我们进行了文献检索,以确定所有关于原发性深静脉血栓形成、原发性肺栓塞和静脉血栓栓塞联合形式患者中杂合子因子V莱顿突变发生率的文章。我们计算了这三种静脉血栓栓塞表现形式(包括当前研究结果)的(共同)比值比。
在92例经证实的肺栓塞患者中,25例(27%)超声检查也异常。在这些患者中,因子V莱顿突变的发生率为24%(95%可信区间9%-45%),而在67例原发性肺栓塞患者中有5例(7%;95%可信区间2%-16%)存在该突变。文献分析表明,原发性深静脉血栓形成、原发性肺栓塞和静脉血栓栓塞联合形式患者中杂合子因子V莱顿突变存在的共同比值比分别为7.9(95%可信区间5-12)、3.5(95%可信区间2-6)和6.8(95%可信区间3-14)。
在原发性肺栓塞患者中,因子V莱顿突变的发生率似乎是原发性深静脉血栓形成患者报告发生率的一半。其机制尚不清楚。