C1QC, VSIG4, and CFD as Potential Peripheral Blood Biomarkers in Atrial Fibrillation-Related Cardioembolic Stroke
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Estimating Bilateral Atrial Function by Cardiovascular Magnetic Resonance Feature Tracking in Patients with Paroxysmal Atrial Fibrillation
Published on: July 20, 2022
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.
Abstract:
Atrial fibrillation (AF) is a major risk factor for ischemic stroke. We aimed to identify novel potential biomarkers with diagnostic value in patients with atrial fibrillation-related cardioembolic stroke (AF-CE).Publicly available gene expression profiles related to AF, cardioembolic stroke (CE), and large artery atherosclerosis (LAA) were downloaded from the Gene Expression Omnibus (GEO). Differentially expressed genes (DEGs) were identified and then functionally annotated. The support vector machine recursive feature elimination (SVM-RFE) and least absolute shrinkage and selection operator (LASSO) regression analysis were conducted to identify potential diagnostic AF-CE biomarkers. Furthermore, the results were validated by using external data sets, and discriminability was measured by the area under the ROC curve (AUC). In order to verify the predictive results, the blood samples of 13 healthy controls, 20 patients with CE, and 20 patients with LAA stroke were acquired for RT-qPCR, and the correlation between biomarkers and clinical features was further explored. Lastly, a nomogram and the companion website were developed to predict the CE-risk rate. Three feature genes (C1QC, VSIG4, and CFD) were selected and validated in the training and the external datasets. The qRT-PCR evaluation showed that the levels of blood biomarkers (C1QC, VSIG4, and CFD) in patients with AF-CE can be used to differentiate patients with AF-CE from normal controls (P < 0.05) and can effectively discriminate AF-CE from LAA stroke (P < 0.05). Immune cell infiltration analysis revealed that three feature genes were correlated with immune system such as neutrophils. Clinical impact curve, calibration curves, ROC, and DCAs of the nomogram indicate that the nomogram had good performance. Our findings showed that C1QC, VSIG4, and CFD can potentially serve as diagnostic blood biomarkers of AF-CE; novel nomogram and the companion website can help clinicians to identify high-risk individuals, thus helping to guide treatment decisions for stroke patients.
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