The genetic risk factors for cerebral venous thrombosis: a case-control study in a Chinese national comprehensive hospital.

IF 2.6 4区 医学 Q2 HEMATOLOGY Thrombosis Journal Pub Date : 2024-06-17 DOI:10.1186/s12959-024-00621-8
Shaoying Wang, Ming Yao, Xinzhuang Yang, Yicheng Zhu, Bin Peng
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Abstract

Background: About 13-25% of cerebral venous thrombosis (CVT) cases lack clear etiology, which may be associated with underlying genetic factors. This study aims to investigate genetic factors in CVT patients using whole exome sequencing (WES).

Methods: Thirty-eight CVT patients hospitalized underwent WES. 977 subjects with WES data from a community cohort study --the Shunyi cohort were as the control group. Using bioinformatics analysis, differential genes with rare damaging variants between two groups were filtered (P < 0.05). KEGG enrichment analysis was performed on the screened genes to identify pathways associated with CVT.

Results: Through analysis of medical history, routine tests, and imaging examinations, the etiology of 38 patients: 8 cases of antiphospholipid syndrome, 6 cases with hematologic diseases, 3 cases of protein C deficiency, and 2 cases of protein S deficiency. Five cases occurred during pregnancy or puerperium, and 3 cases had a history of oral contraceptive use, and so on. The etiology was unknown in 12 cases (31.6%), and the etiology of 4 patients were further clarified through WES: F9 c.838 + 1_838 + 16del, Hemizygote: F9 EX1-EX7 Dup; CBS c.430G > A, CBS c.949 A > G; F2 c.1787G > A; SERPINC1 c.409-11G > T. Comparing the WES data of two groups, a total of 179 different genes with rare damaging variants were screened (P < 0.05), with 5 genes of interest (JAK2, C3, PROC, PROZ, SERPIND1). Enrichment analysis of the 179 different genes revealed the complement and coagulation pathway and the mitogen activated protein kinases (MAPK) pathway were associated with CVT.

Conclusion: For CVT patients with unknown etiology, WES could help identify the cause of CVT early, which is of great significance for treatment decisions and prognosis. In addition to the complement and coagulation pathway, MAPK pathway is associated with CVT, potentially related to platelet regulation and inflammatory response.

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脑静脉血栓形成的遗传风险因素:一项在中国国家综合性医院进行的病例对照研究。
背景:约13-25%的脑静脉血栓(CVT)病例缺乏明确的病因,这可能与潜在的遗传因素有关。本研究旨在利用全外显子组测序(WES)研究 CVT 患者的遗传因素:方法:38 名住院的 CVT 患者接受了 WES 检测。方法:38 名住院的 CVT 患者接受了全外显子组测序,977 名来自社区队列研究--顺义队列--的患者作为对照组。通过生物信息学分析,筛选出两组之间存在罕见损伤性变异的差异基因(P 结果):通过对病史、常规化验和影像学检查的分析,确定了 38 例患者的病因:抗磷脂综合征 8 例,血液病 6 例,蛋白 C 缺乏症 3 例,蛋白 S 缺乏症 2 例。5 例发生在妊娠期或产褥期,3 例有口服避孕药史,等等。12 例(31.6%)病因不明,4 例患者的病因通过 WES 进一步明确:F9 c.838 + 1_838 + 16del,半合子:F9 EX1-EX7 Dup; CBS c.430G > A, CBS c.949 A > G; F2 c.1787G > A; SERPINC1 c.409-11G > T。对比两组的 WES 数据,共筛查出 179 个不同基因的罕见损伤性变异(P 结 论):对于病因不明的 CVT 患者,WES 可帮助其早期确定病因,这对治疗决策和预后判断具有重要意义。除补体和凝血通路外,MAPK 通路也与 CVT 相关,可能与血小板调节和炎症反应有关。
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来源期刊
Thrombosis Journal
Thrombosis Journal Medicine-Hematology
CiteScore
3.80
自引率
3.20%
发文量
69
审稿时长
16 weeks
期刊介绍: Thrombosis Journal is an open-access journal that publishes original articles on aspects of clinical and basic research, new methodology, case reports and reviews in the areas of thrombosis. Topics of particular interest include the diagnosis of arterial and venous thrombosis, new antithrombotic treatments, new developments in the understanding, diagnosis and treatments of atherosclerotic vessel disease, relations between haemostasis and vascular disease, hypertension, diabetes, immunology and obesity.
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