Plasma proteomics uncovers divergent molecular signatures in ischemic stroke and intracerebral hemorrhage
Biomarker Research, 2025
Núñez-Jurado D., Fernández-Vega A., del Río C., Penalba A., Llucià-Carol L., Muiño-Acuña E., Ezcurra-Díaz G., Guasch-Jiménez M., Cullell N., Serrano-Heras G., Arias-Salazar L., Vives-Bauza C., Tur S., Urra X., Castellanos M., Krupinski J., Freijo-Guerrero M., Jiménez-Conde J., Fernández-Pérez I., Segura T., Marti-Fabregas J., Férnandez-Cadenas I., Montaner J.
| Disease area | Application area | Sample type | Products |
|---|---|---|---|
Neurology Neurovascular Diseases | Patient Stratification | Plasma |  Olink Explore 3072/384 |
Abstract
Background
Timely differentiation between ischemic stroke (IS) and intracerebral hemorrhage (ICH) is critical for guiding appropriate acute management strategies. While neuroimaging is the diagnostic gold standard, its accessibility is often limited in urgent clinical settings. Blood biomarkers offer a promising, scalable diagnostic alternative; however, no validated panel is yet available for distinguishing stroke subtypes during the hyperacute phase.
Methods
In a multicenter study, plasma samples were collected within 6 h of symptom onset. A total of 3,072 proteins were measured using Olink® proximity extension assays. We applied differential expression analysis, principal component analysis (PCA), partial least squares discriminant analysis (PLS-DA), and receiver operating characteristic (ROC) curve evaluation. To interpret the biological relevance of the findings, we conducted functional enrichment and protein–protein interaction (PPI) analyses.
Results
Among the 388 patients (344 IS, 44 ICH), 2,531 proteins were retained; 878 reached nominal significance ( p < 0.05), and 67 remained significant after multiple-testing correction (FDR-adjusted p < 0.05). Of these, 844 were overexpressed in ICH and 34 in IS. GFAP, a glial marker, emerged as the most discriminative biomarker for ICH versus IS (AUC = 0.887; sensitivity: 80%, specificity: 90%), followed by BCAN (AUC = 0.820), SNAP25 (AUC = 0.797), and SPOCK1 (AUC = 0.786). For IS, S100A12 (AUC = 0.677) and MNDA (AUC = 0.657) showed the best performance. Multivariate analyses confirmed the presence of distinct proteomic patterns, with enrichment revealing a significant overrepresentation of neurodevelopmental and synaptic pathways. In PPI networks, GFAP and LYN emerged as central hubs.
Conclusion
This study reveals a robust plasma proteomic signature distinguishing IS from ICH within hours of onset. These results lay the groundwork for scalable, blood-based diagnostics to guide early stroke management when imaging is delayed or unavailable.