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Switching off embolization from symptomatic carotid plaque using S-nitrosoglutathione
Zoltan Kaposzta1, John F Martin, Hugh S Markus
1Clinical Neuroscience, St George's Hospital Medical School, London, UK.
S-nitrosoglutathione (GSNO) significantly reduced embolic signals in patients with carotid stenosis, even when they were already on aspirin. This nitric oxide donor offers a promising new approach to prevent recurrent strokes.
Area of Science:
- Neurology
- Vascular Medicine
- Pharmacology
Background:
- Recurrent strokes remain a significant risk despite current antiplatelet therapies.
- Asymptomatic circulating emboli detected by transcranial Doppler ultrasound predict stroke risk in patients with carotid stenosis.
- S-nitrosoglutathione (GSNO), a nitric oxide donor with platelet specificity, was investigated for its anti-embolic potential.
Purpose of the Study:
- To evaluate the effectiveness of GSNO in reducing embolization in patients with symptomatic carotid stenosis.
- To assess the impact of GSNO on embolic signals in patients already treated with aspirin.
Main Methods:
- A double-blind, randomized study involving 20 patients with significant internal carotid artery stenosis.
- Patients received either GSNO or saline placebo for 90 minutes.
- Transcatheter Doppler ultrasound monitored embolic signals in the middle cerebral artery before and up to 24 hours after treatment.
Main Results:
- GSNO treatment led to a rapid and significant reduction in embolic signals: 84% at 0-3 hours, 95% at 6 hours, and 100% at 24 hours.
- These reductions were statistically significant compared to the placebo group (P<0.0001, P=0.003, P<0.0001).
- The mean number of embolic signals per hour before treatment was comparable between groups (6.9 in GSNO vs. 7.3 in placebo).
Conclusions:
- Embolization persists in patients with carotid stenosis despite aspirin therapy.
- GSNO demonstrated high efficacy in rapidly decreasing embolic signals in this high-risk patient group.
- Therapeutic effects of GSNO on embolization lasted for 24 hours, despite short administration and half-life.
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