苏丹孕妇静脉血栓栓塞的危险因素。

IF 0.5 4区 医学 Q4 GENETICS & HEREDITY
Balkan Journal of Medical Genetics Pub Date : 2022-06-05 eCollection Date: 2021-11-01 DOI:10.2478/bjmg-2021-0018
E K Abdalhabib, A Alfeel, E I Ali, I K Ibrahim, A A Mobarki, G Dobie, H A Hamali, M Saboor
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引用次数: 1

摘要

静脉血栓栓塞(VTE)是妊娠相关死亡和发病的主要原因之一。本研究旨在检测VTE孕妇与健康孕妇血清中vleiden因子(FVL)和凝血酶原G20210A多态性的频率,以及血浆中蛋白C (PC)、蛋白S (PS)和抗凝血酶(AT)的水平。本前瞻性病例对照研究确定了198例VTE孕妇和198例健康孕妇FVL G1691A和凝血酶原G20210A多态性的频率,并测量了血浆PC、PS和AT的水平。采用等位基因特异性聚合酶链反应(ASPCR)检测FVL G1691A基因多态性和凝血酶原G20210A基因突变。FVL G1691A多态性和凝血酶原G20210A基因突变仅在VTE孕妇中检测到,频率分别为4.0和0.5%。FVL G1691A多态性在深静脉血栓形成(DVT)患者中频率最高,与避孕使用和终止呈正相关。静脉血栓栓塞孕妇的PC、PS和AT水平明显低于对照组。综上所述,在静脉血栓栓塞患者中,FVL G1691A多态性和PC、PS和AT缺乏是最常见的表现。抗凝血酶缺乏症比PC和PS缺乏症更常见。VTE患者使用避孕药、高体重指数(BMI)和终止妊娠与FVL G1691A多态性、PC和PS缺乏密切相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk Factors of Venous Thromboembolism in Sudanese Pregnant Women.

Venous thromboembolism (VTE) is one of the major causes of pregnancy-related mortality and morbidity. This study aimed to determine the frequency of factor V Leiden (FVL) and prothrombin G20210A polymorphisms and measure the plasma levels of protein C (PC), protein S (PS) and antithrombin (AT) in pregnant women with VTE and healthy pregnant women. This prospective case-control study determined the frequencies of FVL G1691A and prothrombin G20210A polymorphisms and measured the plasma levels of PC, PS and AT in 198 pregnant women with VTE and 198 healthy pregnant women. Allele-specific polymerase chain reaction (ASPCR) was used to detect the FVL G1691A polymorphisms and prothrombin G20210A gene mutations. The FVL G1691A polymorphism and prothrombin G20210A gene mutations were detected only in pregnant women with VTE, with frequencies of 4.0 and 0.5%, respectively. The highest frequency of FVL G1691A polymorphism was observed in patients with deep vein thrombosis (DVT) and positively associated with contraceptive use and termination. Pregnant women with VTE had significantly lower levels of PC, PS and AT than those of controls. In conclusion, among the VTE cases, FVL G1691A polymorphism and PC, PS and AT deficiencies were the most common findings in patients presenting with DVT. Antithrombin deficiency was more common than PC and PS deficiencies. Contraceptive use, high body mass index (BMI) and termination correlated strongly with FVL G1691A polymorphism and PC and PS deficiencies in patients with VTE.

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来源期刊
CiteScore
1.00
自引率
0.00%
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0
审稿时长
>12 weeks
期刊介绍: Balkan Journal of Medical Genetics is a journal in the English language for publication of articles involving all branches of medical genetics: human cytogenetics, molecular genetics, clinical genetics, immunogenetics, oncogenetics, pharmacogenetics, population genetics, genetic screening and diagnosis of monogenic and polygenic diseases, prenatal and preimplantation genetic diagnosis, genetic counselling, advances in treatment and prevention.
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