St. Antonius Hospital, Department of Cardiology, Nieuwegein, the Netherlands (B.K.M., T.O.B., J.M.t.B.).
Division of Hemostasis and Thrombosis, Department of Hematology, UMC Groningen, University of Groningen, The Netherlands (B.K.M.).
Circulation. 2020 Aug 11;142(6):546-555. doi: 10.1161/CIRCULATIONAHA.119.045526. Epub 2020 Jul 13.
Studies examining the role of factor V Leiden among patients at higher risk of atherothrombotic events, such as those with established coronary heart disease (CHD), are lacking. Given that coagulation is involved in the thrombus formation stage on atherosclerotic plaque rupture, we hypothesized that factor V Leiden may be a stronger risk factor for atherothrombotic events in patients with established CHD.
We performed an individual-level meta-analysis including 25 prospective studies (18 cohorts, 3 case-cohorts, 4 randomized trials) from the GENIUS-CHD (Genetics of Subsequent Coronary Heart Disease) consortium involving patients with established CHD at baseline. Participating studies genotyped factor V Leiden status and shared risk estimates for the outcomes of interest using a centrally developed statistical code with harmonized definitions across studies. Cox proportional hazards regression models were used to obtain age- and sex-adjusted estimates. The obtained estimates were pooled using fixed-effect meta-analysis. The primary outcome was composite of myocardial infarction and CHD death. Secondary outcomes included any stroke, ischemic stroke, coronary revascularization, cardiovascular mortality, and all-cause mortality.
The studies included 69 681 individuals of whom 3190 (4.6%) were either heterozygous or homozygous (n=47) carriers of factor V Leiden. Median follow-up per study ranged from 1.0 to 10.6 years. A total of 20 studies with 61 147 participants and 6849 events contributed to analyses of the primary outcome. Factor V Leiden was not associated with the combined outcome of myocardial infarction and CHD death (hazard ratio, 1.03 [95% CI, 0.92-1.16]; =28%; -heterogeneity=0.12). Subgroup analysis according to baseline characteristics or strata of traditional cardiovascular risk factors did not show relevant differences. Similarly, risk estimates for the secondary outcomes including stroke, coronary revascularization, cardiovascular mortality, and all-cause mortality were also close to identity.
Factor V Leiden was not associated with increased risk of subsequent atherothrombotic events and mortality in high-risk participants with established and treated CHD. Routine assessment of factor V Leiden status is unlikely to improve atherothrombotic events risk stratification in this population.
缺乏针对动脉血栓栓塞事件高危患者(如已确诊冠心病 (CHD) 患者)的因子 V 莱顿研究。由于凝血在动脉粥样硬化斑块破裂的血栓形成阶段发挥作用,我们假设因子 V 莱顿在已确诊 CHD 患者中可能是动脉血栓栓塞事件的更强危险因素。
我们进行了一项个体水平的荟萃分析,纳入了来自 GENIUS-CHD(冠心病遗传研究)联盟的 25 项前瞻性研究(18 项队列研究、3 项病例对照研究、4 项随机试验),这些研究的基线均为已确诊 CHD 的患者。参与研究对因子 V 莱顿状态进行基因分型,并使用中央开发的统计代码和跨研究统一的定义共享感兴趣结局的风险估计值。使用 Cox 比例风险回归模型获得年龄和性别调整的估计值。使用固定效应荟萃分析对获得的估计值进行汇总。主要结局为心肌梗死和 CHD 死亡的复合结局。次要结局包括任何卒中、缺血性卒中、冠状动脉血运重建、心血管死亡率和全因死亡率。
这些研究纳入了 69681 名个体,其中 3190 名(4.6%)为杂合子或纯合子(n=47)因子 V 莱顿携带者。每个研究的中位随访时间为 1.0 至 10.6 年。20 项研究(61147 名参与者和 6849 例事件)纳入主要结局分析。因子 V 莱顿与心肌梗死和 CHD 死亡的复合结局无关(风险比,1.03 [95% CI,0.92-1.16];=28%;-异质性=0.12)。根据基线特征或传统心血管危险因素分层的亚组分析未显示出相关差异。同样,卒中、冠状动脉血运重建、心血管死亡率和全因死亡率的次要结局风险估计值也接近一致。
在已确诊和治疗的高危 CHD 患者中,因子 V 莱顿与随后发生的动脉血栓栓塞事件和死亡率增加无关。在该人群中,常规评估因子 V 莱顿状态不太可能改善动脉血栓栓塞事件的风险分层。