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Updated: Aug 8, 2026

Pre-Chiasmatic, Single Injection of Autologous Blood to Induce Experimental Subarachnoid Hemorrhage in a Rat Model
Published on: June 18, 2021
Axonal damage and outcome in subarachnoid haemorrhage
1Department of Neuroimmunology, Institute of Neurology, The National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK. a.petzold@ion.ucl.ac.uk
Axonal degeneration, indicated by elevated neurofilament heavy chain (NfH) levels in cerebrospinal fluid, is common in subarachnoid hemorrhage (SAH) patients and linked to poor outcomes.
Area of Science:
- Neuroscience
- Neurology
- Biomarker Research
Background:
- Subarachnoid hemorrhage (SAH) may involve underestimated axonal degeneration.
- Preliminary evidence suggests axonal damage is a significant pathological feature in SAH.
Purpose of the Study:
- To investigate the presence and significance of axonal degeneration in patients with aneurysmal SAH.
- To correlate levels of a specific biomarker for axonal damage with patient outcomes.
Main Methods:
- A longitudinal study of 17 aneurysmal SAH patients.
- Daily cerebrospinal fluid (CSF) collection for up to 14 days.
- Quantification of neurofilament heavy chain (NfH(SMI35)) using ELISA; Glasgow Outcome Score (GOS) assessed at 3 months.
Main Results:
- Pathologically high NfH levels were found in 52.7% of SAH patient CSF samples, versus 5% in a reference population.
- All patients with poor outcomes (GOS 1-3) showed increased NfH, compared to 8% with good outcomes (GOS 4-5).
- Increased NfH levels correlated with injury severity (WFNS, GCS) and inversely with GOS, becoming significant around 7 days post-hemorrhage.
Conclusions:
- Patients with SAH experience secondary axonal degeneration.
- This axonal degeneration may negatively impact patient outcomes.
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