Service de pneumologie, Hôpital Pontchaillou, Université de Rennes 1, Rue Henri-Le-Guilloux, France.
Université de Brest, EA3878 (GETBO) IFR, Brest, France.
PLoS One. 2018 May 18;13(5):e0194973. doi: 10.1371/journal.pone.0194973. eCollection 2018.
Cancer and factor V Leiden mutation are both risk factors for venous thromboembolism (VTE). Cancer critically increases the thrombotic risk whereas Factor V Leiden is the most common pro-thrombotic mutation. The impact of the factor V Leiden on the risk of VTE in cancer patients remains uncertain.
To assess the impact of factor V Leiden mutation in cancer-associated thrombosis.
The EDITH hospital-based case-control study enrolled 182 patients with cancer and VTE as well as 182 control patients with cancer, matched for gender, age and cancer location, between 2000 and 2012, in the University Hospital of Brest. All cases and controls were genotyped for the factor V Leiden mutation and interviewed with a standardized questionnaire.
Twenty one of 182 (11.5%) patients with cancer-associated thrombosis carried the factor V Leiden mutation and 4 of 182 (2.2%) controls with cancer but no venous thrombosis. In multivariate analysis including cancer stage and family history of VTE, cancer patients with factor V Leiden mutation had a seven-fold increased risk of venous thromboembolism (adjusted odds ratio [OR], 7.04; 95% CI, 2.01-24.63).
The pro-thrombotic Factor V Leiden mutation was found to be an independent additional risk factor for venous thromboembolism in cancer patients and might therefore be considered in the individual thrombotic risk assessment.
癌症和因子 V 莱顿突变都是静脉血栓栓塞症(VTE)的危险因素。癌症极大地增加了血栓形成的风险,而因子 V 莱顿突变是最常见的促血栓形成突变。因子 V 莱顿突变对癌症患者 VTE 风险的影响尚不确定。
评估因子 V 莱顿突变在癌症相关血栓形成中的作用。
这项基于 EDITH 医院的病例对照研究于 2000 年至 2012 年在布雷斯特大学医院纳入了 182 例癌症合并 VTE 的患者和 182 例匹配性别、年龄和癌症部位的癌症但无静脉血栓形成的对照患者。所有病例和对照均进行了因子 V 莱顿突变基因分型,并采用标准化问卷进行了访谈。
182 例癌症相关血栓形成患者中有 21 例(11.5%)携带因子 V 莱顿突变,182 例癌症但无静脉血栓形成的对照中有 4 例(2.2%)。在包括癌症分期和 VTE 家族史的多变量分析中,携带因子 V 莱顿突变的癌症患者发生静脉血栓栓塞症的风险增加了七倍(调整后的优势比 [OR],7.04;95%CI,2.01-24.63)。
促血栓形成的因子 V 莱顿突变被发现是癌症患者静脉血栓栓塞症的一个独立的附加危险因素,因此可以考虑在个体血栓形成风险评估中加以考虑。