ABSTRACT NUMBER: ESOC2026YS268 PROGNOSTIC VALUES OF BIOMARKERS OF INFLAMMATION, STRESS AND DAMAGE-ASSOCIATED DANGER SIGNALLING IN ACUTE ISCHEMIC STROKE: INSIGHTS FROM THE CRESCENDO CONSORTIUM

Abstract Background and aims Patients with ischemic stroke face a high risk of poor outcome and mortality, driven by inflammatory, stress, and tissue-damage mechanisms. Within the European CiRculating mEdiators of Stroke reCurrence anD aetiOlogies (CRESCENDO) consortium, we assessed early serum biomarkers representing inflammation (IL1β, IL6, CRP), stress (copeptin), and damage-associated signalling (HMGB1) as predictors of 3month functional outcome and mortality. Methods Harmonized prospective cohorts from Germany, Spain and Switzerland included 4,854 ischemic stroke patients with serum obtained within 24h of onset. IL1β, IL6, CRP, copeptin, and HMGB1 levels were quantified. Prognostic value for unfavorable outcome (mRS 3–6) and mortality at 3months was evaluated by the change in area under the curve (ΔAUC) between clinical model (NIHSS, age, sex, EssenStrokeRiskScore) and biomarker-augmented models. Results At 3months, 1,603 patients had unfavorable outcomes and 384 had died. For unfavorable outcome, IL-6 showed superior additive value (ΔAUC = 1.2%, 95% CI 0.7–1.7%), followed by copeptin (ΔAUC = 1.0%, 95% CI 0.5–1.5%) and CRP (ΔAUC = 0.6%, 95% CI 0.2–1.0%); the combination of HMGB1, copeptin, and IL6 yielded a ΔAUC = 1.8% (95% CI 1.1–2.4%). For mortality, IL6 performed best (ΔAUC = 3.1%, 95% CI 1.6–4.5%), followed by copeptin (ΔAUC = 2.6%, 95% CI 1.2–4.0%) and CRP (ΔAUC = 2.3%, 95% CI 0.8–3.7%). Combining HMGB1, copeptin and IL6 achieved a ΔAUC = 4.5% (95% CI 2.8–6.2%). Early serum IL6, copeptin, and CRP demonstrated additional prognostic yield for 3month functional outcome and mortality after ischemic stroke, with synergistic performance in combination. Conflict of interest “Johannes Teller: : nothing to disclose”, “Johanna Ernst: : nothing to disclose”, “Alejandro Fernández-Vega: : nothing to disclose”, “Johannes Frenger:: nothing to disclose”, “Hui Jeong Jung:: nothing to disclose”, “Catherine Jutzeler,:: nothing to disclose” “Ralf Lichtinghagen:: nothing to disclose”, “Gerrit M. Grosse:: nothing to disclose”, “Joan Montaner:: nothing to disclose”, “Mira Katan:: nothing to disclose”, on behalf of the CRESCENDO investigators (“Markus Arnold:: nothing to disclose”, “Marcel Arnold:: nothing to disclose”, “Carlo Cereda:: nothing to disclose”, “Carmen Del Río Mercado:: nothing to disclose”, “Gian Marco De Marchis:: nothing to disclose”, “Alejandro Gonzalez:: nothing to disclose”, “Timo Kahles:: nothing to disclose”, “Georg Kägi:: nothing to disclose”, “Francisco Moniche:: nothing to disclose”, “Soledad Perez-Sanchez:: nothing to disclose”, “Ramona Schuppner: nothing to disclose”, “Katharina Spanaus: nothing to disclose”, “Hans Worthmann: nothing to disclose”, “Karin Weissenborn: nothing to disclose”)

Authors

Institutions

Publication Details

Journal
European Stroke Journal
Published
2026-05-01
DOI
https://doi.org/10.1093/esj/aakag023.163
Primary Topic
Neuroinflammation and Neurodegeneration Mechanisms
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

ABSTRACT NUMBER: ESOC2026YS268 PROGNOSTIC VALUES OF BIOMARKERS OF INFLAMMATION, STRESS AND DAMAGE-ASSOCIATED DANGER SIGNALLING IN ACUTE ISCHEMIC STROKE: INSIGHTS FROM THE CRESCENDO CONSORTIUM

Gerrit M. Große, Ralf Lichtinghagen, Joan Montaner, Alejandro Fernández-Vega et al.
European Stroke Journal
Neuroinflammation and Neurodegeneration Mechanisms
article

ABSTRACT NUMBER: ESOC2026YS268 PROGNOSTIC VALUES OF BIOMARKERS OF INFLAMMATION, STRESS AND DAMAGE-ASSOCIATED DANGER SIGNALLING IN ACUTE ISCHEMIC STROKE: INSIGHTS FROM THE CRESCENDO CONSORTIUM

Gerrit M. Große, Ralf Lichtinghagen, Joan Montaner, Alejandro Fernández-Vega, Johannes Teller, Mira Katan, Hui Jeong Jung, Catherine Jutzeler, Johanna Ernst, Frenger Johannes
article en

Abstract

Abstract Background and aims Patients with ischemic stroke face a high risk of poor outcome and mortality, driven by inflammatory, stress, and tissue-damage mechanisms. Within the European CiRculating mEdiators of Stroke reCurrence anD aetiOlogies (CRESCENDO) consortium, we assessed early serum biomarkers representing inflammation (IL1β, IL6, CRP), stress (copeptin), and damage-associated signalling (HMGB1) as predictors of 3month functional outcome and mortality. Methods Harmonized prospective cohorts from Germany, Spain and Switzerland included 4,854 ischemic stroke patients with serum obtained within 24h of onset. IL1β, IL6, CRP, copeptin, and HMGB1 levels were quantified. Prognostic value for unfavorable outcome (mRS 3–6) and mortality at 3months was evaluated by the change in area under the curve (ΔAUC) between clinical model (NIHSS, age, sex, EssenStrokeRiskScore) and biomarker-augmented models. Results At 3months, 1,603 patients had unfavorable outcomes and 384 had died. For unfavorable outcome, IL-6 showed superior additive value (ΔAUC = 1.2%, 95% CI 0.7–1.7%), followed by copeptin (ΔAUC = 1.0%, 95% CI 0.5–1.5%) and CRP (ΔAUC = 0.6%, 95% CI 0.2–1.0%); the combination of HMGB1, copeptin, and IL6 yielded a ΔAUC = 1.8% (95% CI 1.1–2.4%). For mortality, IL6 performed best (ΔAUC = 3.1%, 95% CI 1.6–4.5%), followed by copeptin (ΔAUC = 2.6%, 95% CI 1.2–4.0%) and CRP (ΔAUC = 2.3%, 95% CI 0.8–3.7%). Combining HMGB1, copeptin and IL6 achieved a ΔAUC = 4.5% (95% CI 2.8–6.2%). Early serum IL6, copeptin, and CRP demonstrated additional prognostic yield for 3month functional outcome and mortality after ischemic stroke, with synergistic performance in combination. Conflict of interest “Johannes Teller: : nothing to disclose”, “Johanna Ernst: : nothing to disclose”, “Alejandro Fernández-Vega: : nothing to disclose”, “Johannes Frenger:: nothing to disclose”, “Hui Jeong Jung:: nothing to disclose”, “Catherine Jutzeler,:: nothing to disclose” “Ralf Lichtinghagen:: nothing to disclose”, “Gerrit M. Grosse:: nothing to disclose”, “Joan Montaner:: nothing to disclose”, “Mira Katan:: nothing to disclose”, on behalf of the CRESCENDO investigators (“Markus Arnold:: nothing to disclose”, “Marcel Arnold:: nothing to disclose”, “Carlo Cereda:: nothing to disclose”, “Carmen Del Río Mercado:: nothing to disclose”, “Gian Marco De Marchis:: nothing to disclose”, “Alejandro Gonzalez:: nothing to disclose”, “Timo Kahles:: nothing to disclose”, “Georg Kägi:: nothing to disclose”, “Francisco Moniche:: nothing to disclose”, “Soledad Perez-Sanchez:: nothing to disclose”, “Ramona Schuppner: nothing to disclose”, “Katharina Spanaus: nothing to disclose”, “Hans Worthmann: nothing to disclose”, “Karin Weissenborn: nothing to disclose”)

European Stroke JournalVol. 11(Supplement_1)
Medizinische Hochschule Hannover (DE), ETH Zurich (CH), Hospital Base (CL), Instituto de Biomedicina de Sevilla (ES)
Good health and well-being
Openalex Percentile: Top 9%
Neuroinflammation and Neurodegeneration Mechanisms
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.