Association between factor I fibrinogen (rs6050) and factor XI plasma thromboplastin (rs4253417) genetic polymorphisms and recurrent spontaneous miscarriage in Saudi women.

IF 1.5 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Saudi Medical Journal Pub Date : 2025-02-01 DOI:10.15537/smj.2025.46.2.20240692
Aaishah M Kaabi, Afrah F Alkhuriji, Zeneb A Babay, Ibrahim A Barakat, Abdullah M Kaabi, Reem M Kaabi
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Abstract

Objectives: To identify genetic polymorphisms in factor I fibrinogen (rs6050) and factor XI plasma thromboplastin (rs4253417) in Saudi women with recurrent spontaneous miscarriage (RSM). Furthermore, to compare the levels of clotting factors in the blood of patients and healthy controls.

Methods: The current study was conducted at the King Khalid University Hospital in Riyadh, Saudi Arabia, from September 2022 to June 2023. The study involved 100 Saudi women, 50 pregnant and 50 non-pregnant individuals, who experienced RSM. Furthermore, 100 healthy Saudi women, including 50 pregnant and 50 non-pregnant individuals, were also included as controls. TaqMan genotyping assays were used to determine single nucleotide polymorphisms in the promoter regions of the factor I and XI genes.

Results: A significant correlation was found between the Factor I fibrinogen genotype (rs6050 C/T) and RSM in non-pregnant Saudi women. However, no significant correlation was observed between the Factor XI polymorphism (rs4253417 C/T) and RSM.

Conclusion: We demonstrated a significant correlation between genetic polymorphisms in factor I fibrinogen in certain genes studied and RSM. This association could be attributed to changes in fibrinogen levels, which impact the coagulation process and lead to an increase in thrombotic events, which are recognized as risk factors for miscarriage. Notably, variations in the other genes examined did not exhibit any association with the risk of RSM.

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因子I纤维蛋白原(rs6050)和因子XI血浆凝血活素(rs4253417)遗传多态性与沙特妇女复发性自然流产的关系
目的:研究沙特女性复发性自然流产(RSM)患者的I型纤维蛋白原(rs6050)和XI型血浆凝血酶(rs4253417)基因多态性。此外,比较患者和健康对照者血液中的凝血因子水平。方法:本研究于2022年9月至2023年6月在沙特阿拉伯利雅得的哈立德国王大学医院进行。该研究涉及100名沙特女性,其中50名孕妇和50名非孕妇,她们都经历过RSM。此外,100名健康的沙特妇女,包括50名孕妇和50名非孕妇,也被纳入对照。TaqMan基因分型检测用于确定因子I和XI基因启动子区域的单核苷酸多态性。结果:在非妊娠沙特妇女中,因子I纤维蛋白原基因型(rs6050 C/T)与RSM存在显著相关性。然而,因子XI多态性(rs4253417 C/T)与RSM之间没有显著相关性。结论:我们证明了某些基因中因子I纤维蛋白原的遗传多态性与RSM有显著的相关性。这种关联可能归因于纤维蛋白原水平的变化,其影响凝血过程并导致血栓事件的增加,这被认为是流产的危险因素。值得注意的是,其他基因的变异并没有显示出与RSM的风险有任何关联。
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来源期刊
Saudi Medical Journal
Saudi Medical Journal 医学-医学:内科
CiteScore
2.30
自引率
6.20%
发文量
203
审稿时长
12 months
期刊介绍: The Saudi Medical Journal is a monthly peer-reviewed medical journal. It is an open access journal, with content released under a Creative Commons attribution-noncommercial license. The journal publishes original research articles, review articles, Systematic Reviews, Case Reports, Brief Communication, Brief Report, Clinical Note, Clinical Image, Editorials, Book Reviews, Correspondence, and Student Corner.
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