Rehak Matus, Rehak Jiri, Müller Marc, Faude Susanne, Faude Frank, Siegemund Annelie, Krcova Vera, Slavik Ludek, Hasenclever Dirk, Scholz Markus, Wiedemann Peter
Department of Ophthalmology, University Hospital Leipzig, Liebigstrasse 10-14, 04103 Leipzig, Germany.
Thromb Haemost. 2008 May;99(5):925-9. doi: 10.1160/TH07-11-0658.
Several small case-control studies have investigated whether factor V Leiden (FVL) is a risk factor for retinal vein occlusion (RVO) and generated conflicting data. To clarify this question we performed a large two-centre case-control study and a meta-analysis of published studies. Two hundred seven consecutive patients with RVO and a control group of 150 subjects were screened between 1996 and 2006. A systematic meta-analysis was done combining our study with further 17 published European case-control studies. APC resistance was detected in 16 out of 207 (7.7%) patients and eight out of 150 (5.3%) controls. The odds ratio (OR) estimated was 1.49 with a (non-significant) 95% confidence interval (CI) of 0.62-3.57. The meta-analysis including 18 studies with a total of 1,748 patients and 2,716 controls showed a significantly higher prevalence of FVL in patients with RVO compared to healthy controls (combined OR 1.66; 95% CI 1.19-2.32). All single studies combined in the meta-analysis were too small to reliably detect the effect individually. This explains the seemingly contradictory data in the literature. In conclusion, the prevalence of APC resistance (and FVL) is increased in patients with RVO compared to controls, but the effect is only moderate. Therefore, there is no indication for general screening of factor V mutation in all patients with RVO. We recommend this test to be performed in patients older than 50 years with an additional history of thromboembolic event and in younger patients without general risk factors like hypertension.
几项小型病例对照研究调查了凝血因子V莱顿突变(FVL)是否为视网膜静脉阻塞(RVO)的危险因素,但得出的数据相互矛盾。为了阐明这个问题,我们进行了一项大型的两中心病例对照研究以及已发表研究的荟萃分析。在1996年至2006年间,对207例连续的RVO患者和150名对照组受试者进行了筛查。将我们的研究与另外17项已发表的欧洲病例对照研究相结合,进行了系统的荟萃分析。在207例患者中有16例(7.7%)检测到活化部分凝血活酶时间(APTT)抵抗,在150名对照组中有8例(5.3%)检测到。估计的比值比(OR)为1.49,95%置信区间(CI)为0.62 - 3.57(无统计学意义)。包括18项研究(共1748例患者和2716名对照)的荟萃分析显示,与健康对照组相比,RVO患者中FVL的患病率显著更高(合并OR 1.66;95% CI 1.19 - 2.32)。荟萃分析中纳入的所有单项研究规模都太小,无法单独可靠地检测出这种效应。这就解释了文献中看似矛盾的数据。总之,与对照组相比,RVO患者中APTT抵抗(和FVL)的患病率有所增加,但这种效应仅为中等程度。因此,没有指征对所有RVO患者进行凝血因子V突变的常规筛查。我们建议对年龄大于50岁且有血栓栓塞事件额外病史的患者以及没有高血压等一般危险因素的年轻患者进行此项检测。