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子痫前期和妊娠高血压疾病中的易栓症突变

Thrombophilic mutations in pre-eclampsia and pregnancy-induced hypertension.

作者信息

Omar Siti Z, Qvist Rajes, Khaing Si L, Muniandy Sekaran, Bhalla Sunil

机构信息

Department of Obstetrics and Gynecology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.

出版信息

J Obstet Gynaecol Res. 2008 Apr;34(2):174-8. doi: 10.1111/j.1447-0756.2008.00755.x.

Abstract

AIM

The aim of the present study was to determine the existence or prevalence of thrombophilic markers such as Factor V Leiden, prothrombin G20210A, protein S, protein C, activated protein C and anti-thrombin in pre-eclampsia and pregnancy-induced hypertensive patients.

METHODS

Blood samples were collected from a total number of 124 women at the maternity unit, University of Malaya Medical Center. These included 49 patients with pre-eclampsia, 63 patients with pregnancy-induced hypertension and 12 normal pregnant women. DNA was extracted from the blood samples. Factor V Leiden (Taq I) and prothrombin G20210A (Hind III) genotyping was done on polymerase chain reaction-restriction fragment length polymorphism. Anti-thrombin activity and the concentrations of protein C, protein S and activated protein C were measured using the IL Coagulation System (Hemosil).

RESULTS

Of the 124 subjects, one pre-eclampsia patient was homozygous for Factor V Leiden mutation but prothrombin G20210A mutation was not present in any of the subjects. The subject with Factor V Leiden mutation also had a low activated protein C resistance and a low protein S concentration.

CONCLUSIONS

Factor V Leiden mutation is present in the Asian population and may very well serve as one of the genetic factors responsible for pre-eclampsia and other adverse pregnancy outcomes.

摘要

目的

本研究旨在确定血栓形成倾向标志物,如凝血因子V莱顿突变、凝血酶原G20210A突变、蛋白S、蛋白C、活化蛋白C及抗凝血酶在子痫前期和妊娠高血压患者中的存在情况或流行程度。

方法

从马来亚大学医学中心妇产科的124名女性中采集血样。其中包括49例子痫前期患者、63例妊娠高血压患者和12例正常孕妇。从血样中提取DNA。采用聚合酶链反应-限制性片段长度多态性方法进行凝血因子V莱顿(Taq I)和凝血酶原G20210A(Hind III)基因分型。使用IL凝血系统(Hemosil)检测抗凝血酶活性以及蛋白C、蛋白S和活化蛋白C的浓度。

结果

在124名受试者中,1例子痫前期患者为凝血因子V莱顿突变纯合子,但所有受试者均未检测到凝血酶原G20210A突变。具有凝血因子V莱顿突变的受试者同时具有低活化蛋白C抵抗和低蛋白S浓度。

结论

凝血因子V莱顿突变存在于亚洲人群中,很可能是子痫前期和其他不良妊娠结局的遗传因素之一。

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