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基于全外显子组测序探寻孕妇静脉血栓栓塞症的发病机制

刘博 王运菊 高霞 刘孟彬 尚丽

广东医学2024,Vol.45Issue(5):641-646,6.
广东医学2024,Vol.45Issue(5):641-646,6.DOI:10.13820/j.cnki.gdyx.20233575

基于全外显子组测序探寻孕妇静脉血栓栓塞症的发病机制

Exploring the pathogenesis of venous thromboembolism in pregnant women based on whole exome sequencing

刘博 1王运菊 1高霞 1刘孟彬 2尚丽1

作者信息

  • 1. 十堰市人民医院产科(湖北十堰 442000)
  • 2. 武汉亚心总医院妇科(湖北武汉 430056)
  • 折叠

摘要

Abstract

Objective To investigate the significance of whole exome sequencing(WES)in exploring the patho-genic genes of venous thromboembolism(VTE)in pregnant women.Methods From January 2019 to January 2022,pregnant women who underwent their first prenatal examination(between 16-24 weeks of gestation)at Shiyan People's Hospital were recruited and followed up to 42 days after delivery.A total of 12 pregnant women with VTE and 12 controls were included in the study.Blood samples were collected,and sequencing was performed using whole exome sequencing.Destructive variants identified in known thrombophilic genes and rare destructive variants potentially associated with preg-nancy-related VTE were discovered.Results WES detected a total of 360 827 changes in the VTE group.After filte-ring using the criteria of identifying rare pathogenic variants,the candidate variant list was reduced to 8 452,including 6756 variants of uncertain significance(VUS)and 14 potentially pathogenic variants.The samples contained 29 known thrombophilic variants,including 8 missense,3 nonsense,2 splice site deletions,1 protein-altering insertion and/or de-letion,5 frameshift mutations,7 synonymous mutations,and 3 intronic mutations.The top 5 genes with the highest muta-tion frequencies were coagulation factor V(F5,12.24%),followed by coagulation factor 2(F2,10.20%),PROS1(10.20%),PROC(8.16%),and SERPINA10(6.12%).Exon association studies showed that three exonic variants reached suggestive significance,namely TAS2R43(rs200893955,P=3.68 × 10-5),NRCAM(rs1269621,P=5.04 × 10-5,FDR=0.047 8),and ZFP41(rs6558339,P=8.85 × 10-5).Conclusion Pregnancy-related VTE may be pri-marily associated with the presence of known pathogenic variants,including F5,F2,and 14 potentially rare pathogenic va-riants.

关键词

全外显子组测序/孕妇/静脉血栓栓塞症/致病基因

Key words

whole exome sequencing/pregnant women/venous thromboembolism/causative genes

分类

医药卫生

引用本文复制引用

刘博,王运菊,高霞,刘孟彬,尚丽..基于全外显子组测序探寻孕妇静脉血栓栓塞症的发病机制[J].广东医学,2024,45(5):641-646,6.

基金项目

湖北省卫生健康科研基金项目(20210226) (20210226)

广东医学

OACSTPCD

1001-9448

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