Consensus machine learning identifies cell death gene signature for carotid artery stenosis diagnosis

Carotid artery stenosis (CAS) is a major contributor to ischemic stroke, and molecular tools for its early detection remain limited. To address this need, we integrated one in-house RNA-seq cohort with eight public datasets comprising 696 samples, together with proteomic profiling, RT-qPCR, single-cell sequencing, and FYCO1 silencing experiments. From 1,258 curated cell death-related genes, candidates were filtered by logistic regression across cohorts, and ten machine learning algorithms were combined into 105 model configurations to derive a consensus diagnostic classifier. Fourteen genes showed consistent associations with CAS, and the machine learning-derived diagnostic signature (MLDS), consisting of IRF1, FYCO1, and FDFT1, demonstrated the highest cross-cohort performance. FYCO1 downregulation was validated in plaques and blood and supported by single-cell analysis, while functional assays indicated impaired autophagic flux and heightened inflammatory signaling. These findings highlight MLDS as a robust molecular tool that may enhance the precision diagnosis of CAS.

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Publication Details

Journal
iScience
Published
2025-12-13
DOI
https://doi.org/10.1016/j.isci.2025.114397
Primary Topic
Single-cell and spatial transcriptomics
Type
article
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article

Consensus machine learning identifies cell death gene signature for carotid artery stenosis diagnosis

iScience
Single-cell and spatial transcriptomics
article

Consensus machine learning identifies cell death gene signature for carotid artery stenosis diagnosis

article en

Abstract

Carotid artery stenosis (CAS) is a major contributor to ischemic stroke, and molecular tools for its early detection remain limited. To address this need, we integrated one in-house RNA-seq cohort with eight public datasets comprising 696 samples, together with proteomic profiling, RT-qPCR, single-cell sequencing, and FYCO1 silencing experiments. From 1,258 curated cell death-related genes, candidates were filtered by logistic regression across cohorts, and ten machine learning algorithms were combined into 105 model configurations to derive a consensus diagnostic classifier. Fourteen genes showed consistent associations with CAS, and the machine learning-derived diagnostic signature (MLDS), consisting of IRF1, FYCO1, and FDFT1, demonstrated the highest cross-cohort performance. FYCO1 downregulation was validated in plaques and blood and supported by single-cell analysis, while functional assays indicated impaired autophagic flux and heightened inflammatory signaling. These findings highlight MLDS as a robust molecular tool that may enhance the precision diagnosis of CAS.

iScienceVol. 29(2)
Central South University (CN), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Second Xiangya Hospital of Central South University (CN), First Affiliated Hospital of Zhengzhou University (CN), Fu Wai Hospital (CN)
Good health and well-being
Openalex Percentile: Top 38%
Single-cell and spatial transcriptomics
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