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妊娠不良结局中的凝血因子V莱顿突变和凝血酶原G20210A突变

Factor V Leiden and prothrombin G20210A mutations in pregnancies with adverse outcome.

作者信息

Agorastos T, Karavida A, Lambropoulos A, Constantinidis T, Tzitzimikas S, Chrisafi S, Saravelos H, Vavilis D, Kotsis A, Bontis J

机构信息

First University Department of Obstetrics and Gynecology, Medical School, Aristotle University of Thessaloniki, Greece.

出版信息

J Matern Fetal Neonatal Med. 2002 Oct;12(4):267-73. doi: 10.1080/jmf.12.4.267.273.

Abstract

BACKGROUND

Inherited thrombophilia has been associated with obstetric complications through mechanisms that are not yet fully elucidated. The aim of this study was to investigate the relationship between specific obstetric adverse outcomes and factor V Leiden and prothrombin G20210A mutations.

METHODS

Forty-five women with adverse pregnancy outcome defined as severe pre-eclampsia, abruptio placentae, intrauterine growth restriction and stillbirth, were tested for factor V Leiden and prothrombin G20210A mutations. The control group comprised 100 women with at least one normal pregnancy and no history of thrombosis.

RESULTS

Overall, 13 women with one or more of the above-mentioned pregnancy complications (28%) had either thrombophilic mutation, as compared with six in the control group (6%) (p < 0.001, odds ratio (OR) 6.1; 95% confidence interval (CI) 1.9-20). The factor V Leiden mutation was detected in ten of the women with complicated pregnancies (22%) and in four of the controls (4%) (p < 0.001, OR 6.6; 95% CI 1.7-27.2). The prothrombin G20210A mutation was detected in three women in the group with complications (6%) and in two of the controls (2%) (p = 0.17, OR 3.4; 95% CI 0.4-30.5). Compared to controls, the prevalence of the factor V Leiden mutation was significantly higher in the subgroups of severe pre-eclampsia, abruptio placentae and fetal growth restriction. The prevalence of the prothrombin G20210A mutation does not appear to be significantly different from that in the controls in any of the groups studied.

CONCLUSIONS

Our data suggest that inherited thrombophilia, and specifically the factor V Leiden mutation, may be associated with adverse pregnancy outcome. The role of the prothrombin G20210A mutation remains to be elucidated.

摘要

背景

遗传性易栓症已通过尚未完全阐明的机制与产科并发症相关联。本研究的目的是调查特定产科不良结局与因子V莱顿突变和凝血酶原G20210A突变之间的关系。

方法

对45名妊娠结局不良(定义为重度子痫前期、胎盘早剥、胎儿生长受限和死产)的女性进行因子V莱顿突变和凝血酶原G20210A突变检测。对照组包括100名至少有一次正常妊娠且无血栓形成病史的女性。

结果

总体而言,13名患有上述一种或多种妊娠并发症的女性(28%)存在易栓症突变,而对照组中有6名(6%)(p<0.001,比值比(OR)6.1;95%置信区间(CI)1.9 - 20)。在10名妊娠合并症女性(22%)和4名对照组女性(4%)中检测到因子V莱顿突变(p<0.001,OR 6.6;95% CI 1.7 - 27.2)。在并发症组的3名女性(6%)和2名对照组女性(2%)中检测到凝血酶原G20210A突变(p = 0.17,OR 3.4;95% CI 0.4 - 30.5)。与对照组相比,重度子痫前期、胎盘早剥和胎儿生长受限亚组中因子V莱顿突变的患病率显著更高。在所研究的任何组中,凝血酶原G20210A突变的患病率似乎与对照组无显著差异。

结论

我们的数据表明,遗传性易栓症,特别是因子V莱顿突变,可能与不良妊娠结局相关。凝血酶原G20210A突变的作用仍有待阐明。

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