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

Biomarker and genomic analyses reveal molecular signatures of non-cardioembolic ischemic stroke

第一作者:Lingling Ding

通讯作者:Zixiao Li

Biomarker Genomic Non-cardioembolic ischemic stroke

基本信息

  • 负责人:Lingling Ding
  • 数据来源: CNSR-Ⅲ
  • 论文编号:CNSR-Ⅲ20200210
  • 发表时间:2023-05-30

2023-05-30

已发表文章

发表杂志: Signal Transduction and Targeted Therapy

发表类型: Article

影响因子(IF): 39.3

PMID: 37248226 Pubmed原文链接 全文下载

主要研究背景及目的

Deep phenotyping will provide more specificity, new types of big data, and hidden subtypes of complex diseases. Taking a deep-phenotyping approach to ischemic stroke might break the current impasse in progress to better management. We aim to derive stroke phenotypes based on unsupervised analysis of clinical data.

方法

We integrated data from the Third China National Stroke Registry, including clinical phenotypes, biomarkers, and whole-genome sequencing data for 7695 patients with NCIS. We identified 30 molecular clusters based on 63 biomarkers and explored the comprehensive landscape of biological heterogeneity and subpopulations in NCIS. Dimensionality reduction revealed fine-scale subpopulation structures associated with specific biomarkers.

结论

Our study demonstrates the power of large-scale molecular biomarkers and genomics to understand the underlying biological mechanisms of and advance precision medicine for NCIS.

主要结果

The subpopulations with biomarkers for inflammation, abnormal liver and kidney function, homocysteine metabolism, lipid metabolism, and gut microbiota metabolism were associated with a high risk of unfavorable clinical outcomes, including stroke recurrence, disability, and mortality. Several genes encoding potential drug targets were identified as putative causal genes that drive the clusters, such as CDK10, ERCC3, and CHEK2. We comprehensively characterized the genetic architecture of these subpopulations, identified their molecular signatures, and revealed the potential of the polybiomarkers and polygenic prediction for assessing clinical outcomes.