SLAMF1 as a Risk Biomarker for Nontraumatic SAH: Evidence From a Multiomics Study

Our combined analytical approach identified SLAMF1 as a protein associated with increased SAH risk. SLAMF1, a receptor involved in modulating innate and adaptive immune responses, has been implicated in inflammatory and autoimmune diseases. SLAMF1 and related proteins represent promising biomarkers for SAH risk, potentially enhancing risk stratification, guiding preventive strategies, and informing future therapeutic development. Further research is necessary to explore its mechanistic role in SAH development.

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Publication Details

Journal
Stroke
Published
2025-11-12
DOI
https://doi.org/10.1161/strokeaha.125.052604
Primary Topic
Immune Cell Function and Interaction
Type
article
Field-Weighted Citation Impact
0.00
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article

SLAMF1 as a Risk Biomarker for Nontraumatic SAH: Evidence From a Multiomics Study

Lauren Hachmann Sansing, Murat Günel, Cyprien A. Rivier, Andrew B. Koo et al.
Stroke
Immune Cell Function and Interaction
article

SLAMF1 as a Risk Biomarker for Nontraumatic SAH: Evidence From a Multiomics Study

Lauren Hachmann Sansing, Murat Günel, Cyprien A. Rivier, Andrew B. Koo, Guido J. Falcone, Kevin Navin Sheth, Daniela Renedo, Santiago Clocchiatti‐Tuozzo, Ryan Hebert, Nanthiya Sujijantarat, Shufan Huo, Julián Acosta, Charles Matouk
article en

Abstract

Our combined analytical approach identified SLAMF1 as a protein associated with increased SAH risk. SLAMF1, a receptor involved in modulating innate and adaptive immune responses, has been implicated in inflammatory and autoimmune diseases. SLAMF1 and related proteins represent promising biomarkers for SAH risk, potentially enhancing risk stratification, guiding preventive strategies, and informing future therapeutic development. Further research is necessary to explore its mechanistic role in SAH development.

StrokeVol. 57(2)
Harvard University (US), Yale University (US), Anna Needs Neuroblastoma Answers (US), Norwegian Womens Public Health Association (NO)
Openalex Percentile: Top 64%
Immune Cell Function and Interaction
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