国家神经系统疾病临床医学研究中心数据管理与共享系统

Data Management And Sharing System of China National Clinical Research Center for Neurological Diseases

Somatic mutation contributing to clonal haematopoiesis is a risk factor of recurrent stroke in first-ever acute ischaemic stroke: a prospective cohort study

第一作者:Xin Qiu

通讯作者:Yongjun Wang,Zixiao Li

clonal haematopoiesis of indeterminate potential stroke

基本信息

  • 负责人:Xin Qiu
  • 数据来源: CNSR-Ⅲ
  • 论文编号:CNSR-Ⅲ20200229
  • 发表时间:2022-09-21

2022-09-21

已发表文章

发表杂志:Stroke and vascular neurology

发表类型: Original Articles

影响因子(IF): 9.893

PMID: 36137598 Pubmed原文链接 全文下载

主要研究背景及目的

Clonal hematopoiesis of indeterminate potential (CHIP) is used to describe people who have recurrent mutations in genes related to hematologic malignancies but without a diagnosis of any hematologic malignancy or other clonal disorder. Evidence showed that presence of CHIP was increase with age and it was significantly associated with the risk for coronary heart disease. However, few studies focus on the mechanisms of CHIP in stroke recurrence. Thus, our study aims to assess the incidence of CHIP in patients with stroke and investigate the potential mechanisms of CHIP in stroke recurrence.

方法

We studied a prospective cohort of 6016 patients who had a first-ever AIS in China. Whole-genome sequencing was performed to identify CHIP. High-sensitivity C reactive protein (hs-CRP) levels above 3 mg/L at baseline were defined as hyperinflammation. Recurrent stroke during the 3-month follow-up was the primary outcome.

结论

Our results suggest that somatic mutations contributing to CHIP increase the risk of short-term recurrent stroke in patients who had a first-ever AIS. Hyperinflammation may be important in the relationship between CHIP and recurrent stroke.

主要结果