Key result
Adding endostatin, TNF-R1, and IL-6 to clinical predictors improves long-term mortality discrimination after ischemic stroke.
Why the study?
Stroke is a major cause of disability and death globally, and predicting mortality remains a crucial challenge.
Do blood biomarkers (endostatin, TNF-R1, IL-6) measured during acute ischemic stroke predict long-term mortality?
Cohort (n=941)
Do blood biomarkers (endostatin, TNF-R1, IL-6) measured during acute ischemic stroke predict long-term mortality?
Effect estimate: IDI 0.022 (95% CI 0.007-0.048)
p-value: p=< 0.001
Circulating levels of endostatin, TNF-R1, and IL-6 measured at admission can improve the prediction of long-term mortality after ischemic stroke when added to standard clinical variables.
Biomarker panel modestly improved post-stroke mortality discrimination; hypothesis-generating and requires prospective validation before clinical use.
Stroke is a major cause of disability and death globally, and prediction of mortality represents a crucial challenge. We aimed to identify blood biomarkers measured during acute ischemic stroke that could predict long-term mortality. Nine hundred and forty-one ischemic stroke patients were prospectively recruited in the Stroke-Chip study. Post-stroke mortality was evaluated during a median 4.8-year follow-up. A 14-biomarker panel was analyzed by immunoassays in blood samples obtained at hospital admission. Biomarkers were normalized and standardized using Z-scores. Multiple Cox regression models were used to identify clinical variables and biomarkers independently associated with long-term mortality and mortality due to stroke. In the multivariate analysis, the independent predictors of long-term mortality were age, female sex, hypertension, glycemia, and baseline National Institutes of Health Stroke Scale (NIHSS) score. Independent blood biomarkers predictive of long-term mortality were endostatin > quartile 2, tumor necrosis factor receptor-1 (TNF-R1) > quartile 2, and interleukin (IL)-6 > quartile 2. The risk of mortality when these three biomarkers were combined increased up to 69%. The addition of the biomarkers to clinical predictors improved the discrimination (integrative discriminative improvement (IDI) 0.022 (0.007–0.048), p < 0.001). Moreover, endostatin > quartile 3 was an independent predictor of mortality due to stroke. Altogether, endostatin, TNF-R1, and IL-6 circulating levels may aid in long-term mortality prediction after stroke.
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Ramiro et al. (2021) conducted a cohort in Acute ischemic stroke (n=941). Blood biomarkers (endostatin, TNF-R1, IL-6) vs. Clinical predictors alone was evaluated on Long-term mortality (IDI 0.022, 95% CI 0.007-0.048, p=< 0.001). Combining endostatin, TNF-R1, and IL-6 with clinical predictors improved discrimination for long-term mortality after ischemic stroke (IDI 0.022; 95% CI 0.007-0.048; p<0.001).
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