C1QC, VSIG4, and CFD as Potential Peripheral Blood Biomarkers in Atrial Fibrillation-Related Cardioembolic Stroke

Qian Ding1, Juan Xing2, Fanghui Bai2

  • 1Henan Provincial Engineering Laboratory of Insects Bio-Reactor, Nanyang Normal University, Nanyang, China.

Insights

Researchers identified C1QC, VSIG4, and CFD as potential blood biomarkers for atrial fibrillation-related cardioembolic stroke (AF-CE). A new nomogram and website aid in identifying high-risk individuals for stroke, guiding treatment decisions.

Area of Science:

  • Biomarkers and Stroke Research
  • Genomics and Bioinformatics
  • Cardiovascular Disease Epidemiology

Background:

  • Atrial fibrillation (AF) is a significant risk factor for ischemic stroke.
  • Identifying specific biomarkers for atrial fibrillation-related cardioembolic stroke (AF-CE) is crucial for early diagnosis and management.
  • Current diagnostic methods may lack specificity for differentiating stroke subtypes.

Purpose of the Study:

  • To identify novel diagnostic biomarkers for atrial fibrillation-related cardioembolic stroke (AF-CE).
  • To develop a predictive model for assessing CE risk in patients.
  • To validate the diagnostic and prognostic capabilities of identified biomarkers.

Main Methods:

  • Utilized Gene Expression Omnibus (GEO) datasets for differential gene expression analysis.
  • Applied machine learning algorithms (SVM-RFE, LASSO) to identify candidate biomarkers.
  • Validated biomarker performance using external datasets and RT-qPCR on patient blood samples.
  • Developed a nomogram and companion website for clinical risk prediction.

Main Results:

  • Three key genes (C1QC, VSIG4, CFD) were identified as potential diagnostic biomarkers for AF-CE.
  • RT-qPCR confirmed the differential expression of C1QC, VSIG4, and CFD in AF-CE patients compared to controls and LAA stroke patients.
  • The developed nomogram demonstrated good predictive performance, validated by ROC and DCA analyses.
  • Immune cell infiltration analysis indicated a correlation between these biomarkers and the immune system, particularly neutrophils.

Conclusions:

  • C1QC, VSIG4, and CFD show promise as novel blood biomarkers for diagnosing AF-CE.
  • The developed nomogram and website offer a valuable tool for clinicians to identify high-risk individuals and guide stroke management.
  • These findings contribute to improved diagnostic strategies and personalized treatment approaches for stroke patients.

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