Related Experiment Video
Updated: Jul 12, 2025

Double Direct Injection of Blood into the Cisterna Magna as a Model of Subarachnoid Hemorrhage
Published on: August 30, 2020
Cerebrospinal Fluid and Serum Biomarker Insights in Aneurysmal Subarachnoid Haemorrhage: Navigating the Brain-Heart
Małgorzata Burzyńska1, Agnieszka Uryga2, Rafał Załuski3
1Clinical Department of Anaesthesiology and Intensive Care, Wroclaw Medical University, 50-367 Wroclaw, Poland.
Insights
Severe cardiac dysfunction after aneurysmal subarachnoid hemorrhage (aSAH) is linked to brain and cardiac biomarkers. These markers, including S100B, NSE, and tau protein, may help predict cardiac complications and patient outcomes.
Area of Science:
- Neuroscience
- Cardiology
- Biomarkers
Background:
- Severe cardiac dysfunction is a known complication of aneurysmal subarachnoid hemorrhage (aSAH), but its underlying pathophysiological mechanisms remain unclear.
- Understanding the brain-heart relationship is crucial for managing aSAH patients.
- This study investigates brain-specific and cardiac-specific biomarkers, alongside cerebral autoregulation and autonomic nervous system parameters.
Purpose of the Study:
- To explore the association between brain and cardiac biomarkers in aSAH patients.
- To identify potential predictors of severe cardiac complications following aSAH.
- To investigate the relationship between cerebral autoregulation, autonomic function, and cardiac outcomes in aSAH.
Main Methods:
- Analysis of cerebrospinal fluid (CSF) and serum biomarkers (S100B, NSE, tau protein, GFAP, BNP, troponin I) in 15 aSAH patients.
- Assessment of cerebral autoregulation and heart rate variability (HRV LF/HF ratio).
- Correlation analysis to determine relationships between biomarkers and clinical parameters.
Main Results:
- Significant correlations were found between CSF S100B and BNP, CSF NSE and troponin I/BNP, and CSF tau protein and BNP.
- Patients with severe cardiac complications had higher serum tau protein levels on day 1.
- Elevated serum NSE correlated with impaired cerebral autoregulation, and HRV LF/HF ratio correlated with GFAP and S100B.
Conclusions:
- Brain and cardiac biomarkers show potential for early detection of cardiac complications in aSAH.
- Biomarker profiles may aid clinicians in assessing prognosis and guiding patient management.
- Further research is warranted to validate these findings in larger cohorts.
Abstract:
The pathophysiological mechanisms underlying severe cardiac dysfunction after aneurysmal subarachnoid haemorrhage (aSAH) remain poorly understood. In the present study, we focused on two categories of contributing factors describing the brain-heart relationship. The first group includes brain-specific cerebrospinal fluid (CSF) and serum biomarkers, as well as cardiac-specific biomarkers. The secondary category encompasses parameters associated with cerebral autoregulation and the autonomic nervous system. A group of 15 aSAH patients were included in the analysis. Severe cardiac complications were diagnosed in seven (47%) of patients. In the whole population, a significant correlation was observed between CSF S100 calcium-binding protein B (S100B) and brain natriuretic peptide (BNP) (rS = 0.62; p = 0.040). Additionally, we identified a significant correlation between CSF neuron-specific enolase (NSE) with cardiac troponin I (rS = 0.57; p = 0.025) and BNP (rS = 0.66; p = 0.029), as well as between CSF tau protein and BNP (rS = 0.78; p = 0.039). Patients experiencing severe cardiac complications exhibited notably higher levels of serum tau protein at day 1 (0.21 ± 0.23 [ng/mL]) compared to those without severe cardiac complications (0.03 ± 0.04 [ng/mL]); p = 0.009. Impaired cerebral autoregulation was noted in patients both with and without severe cardiac complications. Elevated serum NSE at day 1 was related to impaired cerebral autoregulation (rS = 0.90; p = 0.037). On the first day, a substantial, reciprocal correlation between heart rate variability low-to-high frequency ratio (HRV LF/HF) and both GFAP (rS = -0.83; p = 0.004) and S100B (rS = -0.83; p = 0.004) was observed. Cardiac and brain-specific biomarkers hold the potential to assist clinicians in providing timely insights into cardiac complications, and therefore they contribute to the prognosis of outcomes.
More Related Videos
Related Concept Videos
Blood Studies for Cardiovascular System II: CRP, Hcy, and Cardiac Natriuretic Peptide Markers
These markers indicate stress or strain on the heart muscle:
Natriuretic Peptides (BNP)
Cardiac myocytes produce these hormones in response to ventricular stretching...
Blood Studies for Cardiovascular System I: Cardiac Biomarkers
The essential diagnostic tools for detecting myocardial necrosis and monitoring individuals suspected of having acute coronary syndrome (ACS) include:
Troponins
Troponins, particularly cardiac troponins I and T, are the most precise and sensitive markers of myocardial injury. They are detectable within 4-6 hours of myocardial injury and remain...
Cerebrospinal Fluid
CSF Production
CSF is produced mainly in the choroid plexus, a network of capillaries and ependymal cells located within the ventricular system of the brain....

