Elevated serum S100B levels in the acute phase of ischemic stroke were independently associated with increased mortality risk, and a combined measure of S100B, high-sensitivity C-reactive protein, and platelet count may further improve risk stratification.
Key Findings
Results
Higher baseline serum S100B levels were associated with increased risk of death after ischemic stroke.
Each SD increase in log-transformed serum S100B was associated with a 38% greater risk of death
A spline regression model showed a linear relationship between serum S100B and death risk (Plinearity=0.006)
92 (2.8%) patients died during the 3-month follow-up period
Results
Significant joint effects were observed between S100B and high-sensitivity C-reactive protein (hs-CRP) in association with death after ischemic stroke.
The joint effect of elevated S100B and elevated hs-CRP was associated with increased mortality risk
The highest risk of death was observed among patients with elevations in all three biomarkers (S100B, hs-CRP, and platelet count)
These joint effects were statistically significant as reported in multivariable-adjusted models
Results
Significant joint effects were observed between S100B and platelet count in association with death after ischemic stroke.
Elevated platelet count combined with elevated S100B was associated with increased mortality risk
The combination of all three biomarkers (S100B, hs-CRP, and platelet count) identified the highest-risk patients
Results were derived from multivariable-adjusted Cox proportional hazards regression models
Methods
The study population consisted of 3249 patients with acute ischemic stroke enrolled in a prospective multicenter cohort across China.
Data were derived from 26 hospitals across China
Serum S100B concentrations were measured at baseline (acute phase)
Patients were followed up for 3 months after ischemic stroke
Study outcomes included death, major disability, and vascular events
The trial was registered at ClinicalTrials.gov (NCT01840072)
Results
Elevated serum S100B levels were independently associated with increased mortality risk after adjustment for potential confounders.
Multivariable-adjusted Cox proportional hazards regression models and logistic regression models were applied
Hazard ratios (HRs) or odds ratios (ORs) and their 95% CIs were estimated
S100B has been linked to blood-brain barrier disruption and neuroinflammation
The association with death was independent, suggesting S100B provides prognostic information beyond existing clinical variables
Conclusions
A combined measure of S100B, hs-CRP, and platelet count may improve risk stratification after ischemic stroke.
The three biomarkers together captured joint inflammatory and thrombotic pathophysiological pathways
The highest death risk was observed in patients with simultaneous elevations in all three biomarkers
S100B reflects blood-brain barrier disruption and neuroinflammation, hs-CRP reflects systemic inflammation, and platelet count reflects thrombotic activity
Authors suggest a single combined biomarker measure could further improve prognostic accuracy
What This Means
This research suggests that measuring a brain-injury protein called S100B in the blood shortly after an ischemic stroke (a stroke caused by a blocked blood vessel) can help predict which patients are at greatest risk of dying within three months. Among 3,249 stroke patients followed across 26 hospitals in China, those with the highest blood levels of S100B at hospital admission were about twice as likely to die within three months compared to those with the lowest levels, and this relationship was consistent across the full range of S100B values.
This research also suggests that combining S100B with two other commonly measured blood markers — high-sensitivity C-reactive protein (hs-CRP, a marker of body-wide inflammation) and platelet count (related to blood clotting) — provides even better information about a patient's risk. Patients who had high levels of all three markers at the same time faced the greatest risk of death, pointing to a possible interplay between brain injury, inflammation, and clotting processes in determining stroke outcomes.
These findings matter because identifying high-risk stroke patients early could allow clinicians to tailor monitoring and treatment more precisely. S100B is already measurable with standard laboratory equipment, and combining it with hs-CRP and platelet count — tests routinely done in many hospital settings — could offer a practical, low-cost tool for improving stroke prognosis without requiring additional specialized testing.
Yang P, Sun L, Jia Y, Zhu Z, Wang A, Zhang Y, et al.. (2026). Serum S100B and Its Interplay With hs-CRP and Platelet Count in Association With Adverse Outcomes After Ischemic Stroke.. Journal of the American Heart Association. https://doi.org/10.1161/JAHA.125.048160