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印度患者复发性胎儿丢失的血栓形成倾向方面

Thrombophilic dimension of recurrent fetal loss in Indian patients.

作者信息

Vora Sonal, Shetty Shrimati, Ghosh Kanjaksha

机构信息

National Institute of Immunohaematology (ICMR), KEM Hospital, Parel, Mumbai, India.

出版信息

Blood Coagul Fibrinolysis. 2008 Sep;19(6):581-4. doi: 10.1097/MBC.0b013e328304dffc.

Abstract

We studied the prevalence of acquired and genetic thrombophilia in 198 women with recurrent fetal loss who were having three or more than three abortions. Seventy-nine women had only early pregnancy losses, that is, first trimester abortions, 30 women had only late pregnancy losses, that is, second and third trimester abortions whereas 89 had both early and late pregnancy losses. The control group included 100 age-matched fertile parous women who did not have any obstetric complications and had at least one normal healthy child. Several genetic and acquired thrombophilia markers were studied. The strongest association was observed with anticardiolipin (odds ratio 22.6, confidence interval 5.7-89, P = 0) followed by lupus anticoagulant, anti-beta2 glycoprotein-1, antiannexin. Association of antiphospholipid antibody syndromes was detected with the time of pregnancy loss in anticardiolipin, lupus anticoagulants, which was significantly associated with early pregnancy loss as compared with second and third trimester loss. In case of beta2 glycoprotein-1, antiannexin it was less significantly associated with early pregnancy loss as compared with second and third trimester loss. The risk of fetal loss with protein S deficiency was the highest risk observed for any heritable thrombophilia, followed by protein C, factor V Leiden, endothelial protein C receptor, antithrombin III deficiency and beta448 fibrinogen polymorphism. Modest risks were also observed with 5,10-methylenetetrahydrofolate reductase, plasminogen activator inhibitor 4G/4G polymorphisms and beta448 fibrinogen polymorphism. A combination of two or more than two genetic risk factors were observed in 55 (27.7%), whereas the genetic and acquired risk factors were observed in 107 (54%) of the cases. Thrombophilia is an important contributing factor for both early and late pregnancy losses; approximately two-thirds of our cases of unexplained fetal losses could be explained by acquired or heritable thrombophilia or both, which is in line with other western studies.

摘要

我们研究了198例有三次或三次以上流产的复发性流产女性中获得性和遗传性易栓症的患病率。79名女性仅有早期妊娠丢失,即孕早期流产;30名女性仅有晚期妊娠丢失,即孕中期和孕晚期流产;而89名女性既有早期妊娠丢失又有晚期妊娠丢失。对照组包括100名年龄匹配的有生育史的健康女性,她们没有任何产科并发症且至少有一个正常健康的孩子。我们研究了几种遗传性和获得性易栓症标志物。观察到与抗心磷脂的关联最强(优势比22.6,置信区间5.7 - 89,P = 0),其次是狼疮抗凝物、抗β2糖蛋白-1、抗膜联蛋白。抗磷脂抗体综合征与抗心磷脂、狼疮抗凝物妊娠丢失时间相关,与孕中期和孕晚期丢失相比,其与早期妊娠丢失显著相关。对于β2糖蛋白-1、抗膜联蛋白,与孕中期和孕晚期丢失相比,其与早期妊娠丢失的关联不太显著。蛋白S缺乏导致的胎儿丢失风险是所有遗传性易栓症中观察到的最高风险,其次是蛋白C、因子V Leiden、内皮蛋白C受体、抗凝血酶III缺乏和β448纤维蛋白原多态性。5,10 - 亚甲基四氢叶酸还原酶、纤溶酶原激活物抑制剂4G/4G多态性和β448纤维蛋白原多态性也观察到有适度风险。55例(27.7%)观察到两种或两种以上遗传风险因素的组合,而107例(54%)观察到遗传和获得性风险因素的组合。易栓症是早期和晚期妊娠丢失的一个重要因素;我们大约三分之二原因不明的胎儿丢失病例可以用获得性或遗传性易栓症或两者来解释,这与其他西方研究一致。

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