Identification of Novel Biomarkers for Ischemic Stroke Through Integrated Bioinformatics Analysis and Machine Learning

IF 2.8 4区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Juan Jia, Liang Niu, Peng Feng, Shangyu Liu, Hongxi Han, Bo Zhang, Yingbin Wang, Manxia Wang
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Abstract

Ischemic stroke leads to permanent damage to the affected brain tissue, with strict time constraints for effective treatment. Predictive biomarkers demonstrate great potential in the clinical diagnosis of ischemic stroke, significantly enhancing the accuracy of early identification, thereby enabling clinicians to intervene promptly and reduce patient disability and mortality rates. Furthermore, the application of predictive biomarkers facilitates the development of personalized treatment plans tailored to the specific conditions of individual patients, optimizing treatment outcomes and improving prognoses. Bioinformatics technologies based on high-throughput data provide a crucial foundation for comprehensively understanding the biological characteristics of ischemic stroke and discovering effective predictive targets. In this study, we evaluated gene expression data from ischemic stroke patients retrieved from the Gene Expression Omnibus (GEO) database, conducting differential expression analysis and functional analysis. Through weighted gene co-expression network analysis (WGCNA), we characterized gene modules associated with ischemic stroke. To screen candidate core genes, three machine learning algorithms were applied, including Least Absolute Shrinkage and Selection Operator (LASSO), random forest (RF), and support vector machine-recursive feature elimination (SVM-RFE), ultimately identifying five candidate core genes: MBOAT2, CKAP4, FAF1, CLEC4D, and VIM. Subsequent validation was performed using an external dataset. Additionally, the immune infiltration landscape of ischemic stroke was mapped using the CIBERSORT method, investigating the relationship between candidate core genes and immune cells in the pathogenesis of ischemic stroke, as well as the key pathways associated with the core genes. Finally, the key gene VIM was further identified and preliminarily validated through four machine learning algorithms, including generalized linear model (GLM), Extreme Gradient Boosting (XGBoost), RF, and SVM-RFE. This study contributes to advancing our understanding of biomarkers for ischemic stroke and provides a reference for the prediction and diagnosis of ischemic stroke.

通过综合生物信息学分析和机器学习识别缺血性中风的新型生物标记物
缺血性中风会对受影响的脑组织造成永久性损伤,对有效治疗有严格的时间限制。预测性生物标志物在缺血性脑卒中的临床诊断中显示出巨大的潜力,显著提高了早期识别的准确性,从而使临床医生能够及时干预,降低患者的致残率和死亡率。此外,预测性生物标志物的应用有助于针对个别患者的具体情况制定个性化治疗计划,优化治疗结果并改善预后。基于高通量数据的生物信息学技术为全面了解缺血性脑卒中的生物学特性和发现有效的预测靶点提供了重要的基础。在这项研究中,我们评估了从基因表达Omnibus (GEO)数据库中检索的缺血性脑卒中患者的基因表达数据,进行了差异表达分析和功能分析。通过加权基因共表达网络分析(WGCNA),我们表征了与缺血性卒中相关的基因模块。为了筛选候选核心基因,我们使用了三种机器学习算法,包括最小绝对收缩和选择算子(LASSO)、随机森林(RF)和支持向量机递归特征消除(SVM-RFE),最终确定了5个候选核心基因:MBOAT2、CKAP4、FAF1、cle4d和VIM。后续验证使用外部数据集执行。此外,利用CIBERSORT方法绘制缺血性卒中的免疫浸润景观,研究候选核心基因与免疫细胞在缺血性卒中发病机制中的关系,以及与核心基因相关的关键通路。最后,通过广义线性模型(GLM)、极端梯度增强(XGBoost)、RF和SVM-RFE四种机器学习算法进一步识别关键基因VIM并进行初步验证。本研究有助于加深我们对缺血性脑卒中生物标志物的认识,为缺血性脑卒中的预测和诊断提供参考。
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来源期刊
Journal of Molecular Neuroscience
Journal of Molecular Neuroscience 医学-神经科学
CiteScore
6.60
自引率
3.20%
发文量
142
审稿时长
1 months
期刊介绍: The Journal of Molecular Neuroscience is committed to the rapid publication of original findings that increase our understanding of the molecular structure, function, and development of the nervous system. The criteria for acceptance of manuscripts will be scientific excellence, originality, and relevance to the field of molecular neuroscience. Manuscripts with clinical relevance are especially encouraged since the journal seeks to provide a means for accelerating the progression of basic research findings toward clinical utilization. All experiments described in the Journal of Molecular Neuroscience that involve the use of animal or human subjects must have been approved by the appropriate institutional review committee and conform to accepted ethical standards.
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