首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >Should women suffering from migraine with aura be screened for biological thrombophilia?: Results from a cross-sectional French study
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Should women suffering from migraine with aura be screened for biological thrombophilia?: Results from a cross-sectional French study

机译:应当对患有偏头痛先兆的女性进行生物学血栓形成性筛查吗?:法国一项横断面研究的结果

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Introduction Migraine, particularly migraine with aura (MA), is associated with a higher risk for ischemic stroke (IS). A procoagulant state may predispose to IS. Whether inherited biological thrombophilia are associated with migraine risk remains controversial. Objective To assess the risk of migraine without or with aura related to inherited biological thrombophilia adjusted for the main potential confounders. Material and Methods A cross-sectional study was conducted in 1456 French women aged 18 to 56 years, referred for biological coagulation check-up because of personal or familial venous thrombosis history. Between April 2007 and December 2008, all women answered a self-administered questionnaire to determine whether they had headache. Results There were 294 (20%) migrainous sufferers (including 71 [5%] with MA), 975 (67%) non migrainous women and 187 (13%) non migrainous headache women. Inherited thrombophilia were detected in 576 (40%) women, including 389 (40%) non migrainous women, 90 (40%) migraine without aura (MWA), 33 (46%) MA women and 64 (34%) non migrainous headache women. Factor V Leiden (FVL) i.e. F5rs6025 or Factor II G20210A (FIIL) i.e. F2rs1799963 mutation was detected in 296 (30%) non migrainous women and in 100 (34%) migrainous women of which 27 had MA. There was a significant association between MA and FVL or FIIL mutations (adjusted OR = 1.76 [95% CI 1.02-3.06] p = 0.04) whereas this association in MWA and in non migrainous headache women was not significant. There was no significant association between migraine and other biological thrombophilia. Conclusion FVL or FIIL mutations were more likely among patients suffering from MA. Whether biological thrombophilia screening should be systematically performed in women suffering from MA remains to be determined.
机译:简介偏头痛,尤其是先兆性偏头痛(MA),与缺血性中风(IS)的风险较高相关。促凝状态可能易患IS。遗传性生物血友病是否与偏头痛风险有关仍存在争议。目的评估经校正的潜在潜在混杂因素,无偏头痛或无先兆的偏头痛与遗传性生物血栓形成相关的风险。材料和方法在1456名年龄在18至56岁的法国女性中进行了横断面研究,由于个人或家族静脉血栓形成的历史,他们被要求进行生物凝血检查。在2007年4月至2008年12月之间,所有妇女都回答了一份自我管理的问卷,以确定她们是否头痛。结果有294例(20%)偏头痛患者(包括71名[5%]的MA),975例(67%)非偏头痛妇女和187例(13%)非偏头痛妇女。在576名(40%)妇女中检测到遗传性血栓形成,包括389名(40%)非偏头痛妇女,90名(40%)无先兆偏头痛(MWA),33名(46%)MA妇女和64名(34%)非偏头痛女人。在296名(30%)非移民妇女和100名(34%)移民妇女中检出了因子V莱顿(FVL)即F5rs6025或因子II G20210A(FIIL)即F2rs1799963突变,其中27名患有MA。 MA和FVL或FIIL突变之间存在显着关联(校正OR = 1.76 [95%CI 1.02-3.06] p = 0.04),而在MWA和非偏头痛妇女中这种关联并不显着。偏头痛与其他生物学性血栓形成症之间没有显着关联。结论MA患者中FVL或FIIL突变的可能性更高。是否应该对患有MA的女性进行系统的生物血栓形成性筛查尚待确定。

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