Evidence map›Paper›PMID 39477876›Full record

ArticleMolecular neurobiology2025

Serum EpCAM or PECAM Levels and Risk of Ischemic Stroke: A Two-Sample Mendelian Randomization Study.

Gao Yikun, Li Yilin, Li Yina, Wang Jin, Cai Qiang, Gu Lijuan

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Article in Molecular neurobiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Gao Yikun *Central Laboratory, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
Li Yilin *Central Laboratory, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
Li YinaCentral Laboratory, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
Wang JinCentral Laboratory, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
Cai Qiang *Department of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, 430060, China. caiqno@whu.edu.cn.
Gu Lijuan *Central Laboratory, Renmin Hospital of Wuhan University, Wuhan, 430060, China. gulijuan@whu.edu.cn.

Funding

National Natural Science Foundation of China 82271370National Natural Science Foundation of China 82271518
6 · The paper itself

Abstract

Elevated serum Epithelial cell adhesion molecule (EpCAM) or Platelet endothelial cell adhesion molecule (PECAM) are associated with ischemic stroke (IS), but the causality remains unclear. A two-sample Mendelian randomization (MR) study was performed to examine the causal effect of serum EpCAM or PECAM levels on the risk of IS subtypes.The study utilized GWAS datasets from European and African American populations to identify SNPs associated with serum EpCAM and PECAM levels as instrumental variables. These were then used in MR analyses for IS subtypes, employing multiple methods including IVW, weighted median, MR-Egger, and maximum likelihood. Sensitivity analyses were conducted to validate the results. No significant causal association was observed for EpCAM levels with any of three IS subtypes. Main IVW MR analysis indicated that serum PECAM levels were negatively related to the incidence of large artery stroke (LAS), small vessel stroke (SVS), and cardioembolic stroke (CES), especially CES. Sensitivity analyses confirmed the robustness of these results. Our study reveals a negative correlation between genetically predicted PECAM levels and ischemic stroke risk, particularly for cardioembolic stroke, suggesting PECAM's potential as a biomarker for risk stratification. While no clear causal relationship was found for EpCAM, these findings have significant implications for stroke prevention and treatment strategies. Further research is needed to validate these results and explore their clinical applications, potentially leading to more personalized approaches in stroke management.

Indexed as

Epithelial Cell Adhesion MoleculeIschemic StrokeMendelian Randomization AnalysisPlatelet Endothelial Cell Adhesion Molecule-1Genetic Predisposition to DiseaseGenome-Wide Association StudyHumansPolymorphism, Single NucleotideRisk FactorsEPCAM protein, humanEpithelial Cell Adhesion MoleculePECAM1 protein, humanPlatelet Endothelial Cell Adhesion Molecule-1Epithelial Cell Adhesion MoleculeGenome-Wide Association StudyIschemic StrokeMendelian RandomizationPlatelet Endothelial Cell Adhesion Molecule

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.