Slooter A J C, Rosendaal F R, Tanis B C, Kemmeren J M, van der Graaf Y, Algra A
Department of Neurology, Rudolf Magnus Institute of Neuroscience, University Medical Center, Utrecht, The Netherlands.
J Thromb Haemost. 2005 Jun;3(6):1213-7. doi: 10.1111/j.1538-7836.2005.01442.x.
The role of inherited prothrombotic conditions, including factor V Leiden (FV G1691A), prothrombin G20210A, and the methylenetetrahydrofolate reductase (MTHFR) C677T genotype, in the pathogenesis of ischemic stroke is not well established. The effects of these factors may be potentiated by the use of oral contraceptives, analogous to observations in venous thrombosis.
Patients (n = 193) were women aged 20-49 years with ischemic stroke. Controls (n = 767) were women without arterial thrombosis stratified for age, calendar year of the index event, and residence. The relative risk of ischemic stroke was estimated with unconditional logistic regression, adjusted for stratification variables.
Factor V Leiden and MTHFR 677TT were more common in patients than in controls [odds ratio (OR): 1.8; 95% confidence interval (CI): 0.9-3.6 respectively OR: 1.5; 95% CI: 0.9-2.6]. The frequency of prothrombin G20210A was similar in cases and controls. Carriers of FV Leiden using oral contraceptives had a 11.2-fold (95% CI: 4.3-29.0) higher risk of ischemic stroke than women without either risk factor. Women with MTHFR 677TT using oral contraceptives had a 5.4-fold (95% CI: 2.4-12.0) higher risk than women without these risk factors.
These data suggest that carriers of FV Leiden or MTHFR 677TT who use oral contraceptives have an increased risk of ischemic stroke. When these findings are confirmed, a cost-effectiveness analysis should indicate whether ischemic stroke could be prevented with genetic testing before the start of oral contraceptives.
遗传性血栓形成倾向,包括因子V莱顿突变(FV G1691A)、凝血酶原G20210A以及亚甲基四氢叶酸还原酶(MTHFR)C677T基因型,在缺血性卒中发病机制中的作用尚未完全明确。与静脉血栓形成的观察结果类似,口服避孕药可能会增强这些因素的影响。
研究对象为193例年龄在20 - 49岁的缺血性卒中女性患者。对照组(n = 767)为无动脉血栓形成的女性,根据年龄、索引事件发生年份和居住地进行分层。采用无条件逻辑回归估计缺血性卒中的相对风险,并对分层变量进行校正。
因子V莱顿突变和MTHFR 677TT在患者中的发生率高于对照组[比值比(OR)分别为:1.8;95%置信区间(CI):0.9 - 3.6;OR:1.5;95% CI:0.9 - 2.6]。凝血酶原G20210A在病例组和对照组中的频率相似。使用口服避孕药的因子V莱顿突变携带者发生缺血性卒中的风险比无任何危险因素的女性高11.2倍(95% CI:4.3 - 29.0)。使用口服避孕药的MTHFR 677TT女性发生缺血性卒中的风险比无这些危险因素的女性高5.4倍(95% CI:2.4 - 12.0)。
这些数据表明,使用口服避孕药的因子V莱顿突变或MTHFR 677TT携带者发生缺血性卒中的风险增加。若这些发现得到证实,成本效益分析应表明在开始口服避孕药前进行基因检测是否可预防缺血性卒中。