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Association between systemic inflammation biomarkers and outcomes in patients with aneurysmal subarachnoid hemorrhage
Maria Della Giovampaola1,2, Andrea Vieno1,3, Adeline Higuet4
1Department of Intensive Care, Hôpital Universitaire de Bruxelles (HUB), Université Libre de Bruxelles (ULB), Brussels, Belgium.
Aneurysmal subarachnoid hemorrhage (aSAH) is a devastating condition that is associated with cerebral and systemic inflammation. C-reactive protein (CRP) and neutrophil-to-lymphocyte ratio (NLr) are easily available biomarkers of systemic inflammation. Therefore, we aimed to assess the impact of elevated CRP and NLr on aSAH outcomes. This retrospective, single-center study included adult patients admitted with aSAH to the intensive care unit (ICU) from January 2007 to December 2023. We recorded serum CRP and NLr levels during the first 7 days of ICU stay. An unfavorable neurological outcome at 3 months was defined as a Glasgow Outcome Scale (GOS) score of 1-3. A total of 547 patients were included in the study; 250 (45.7%) experienced unfavorable outcomes (UOs), and 140 (25.6%) developed delayed cerebral ischemia (DCI). Patients with unfavorable outcomes had higher levels of CRP from days 2 to 7 after SAH (p = 0.001) and higher NLr (p = 0.06) than those with favorable outcomes (FOs). In a multivariate logistic regression model, the highest CRP value (OR: 1.003, 95% CI: 1.001-1.005) and the highest NLr value (OR: 1.025; 95% CI: 1.001-1.050) in the first 7 days after SAH were independently associated with the occurrence of unfavorable outcomes. The highest NLr value was also associated with the development of DCI (sHR: 1.02, 95% CI: 1.01-1.03). In conclusion, high CRP and NLr values have a significant prognostic role in aSAH patients, reinforcing the importance of inflammation as a potential mechanism of secondary brain injury.
Aneurysmal subarachnoid hemorrhage (aSAH) is a devastating condition that is associated with cerebral and systemic inflammation. C-reactive protein (CRP) and neutrophil-to-lymphocyte ratio (NLr) are easily available biomarkers of systemic inflammation. Therefore, we aimed to assess the impact of elevated CRP and NLr on aSAH outcomes. This retrospective, single-center study included adult patients admitted with aSAH to the intensive care unit (ICU) from January 2007 to December 2023. We recorded serum CRP and NLr levels during the first 7 days of ICU stay. An unfavorable neurological outcome at 3 months was defined as a Glasgow Outcome Scale (GOS) score of 1-3. A total of 547 patients were included in the study; 250 (45.7%) experienced unfavorable outcomes (UOs), and 140 (25.6%) developed delayed cerebral ischemia (DCI). Patients with unfavorable outcomes had higher levels of CRP from days 2 to 7 after SAH (p = 0.001) and higher NLr (p = 0.06) than those with favorable outcomes (FOs). In a multivariate logistic regression model, the highest CRP value (OR: 1.003, 95% CI: 1.001-1.005) and the highest NLr value (OR: 1.025; 95% CI: 1.001-1.050) in the first 7 days after SAH were independently associated with the occurrence of unfavorable outcomes. The highest NLr value was also associated with the development of DCI (sHR: 1.02, 95% CI: 1.01-1.03). In conclusion, high CRP and NLr values have a significant prognostic role in aSAH patients, reinforcing the importance of inflammation as a potential mechanism of secondary brain injury.

