The effect of allopurinol on the cerebral vasculature of patients with subcortical stroke; a randomized trial

Dawson, J., Quinn, T.J., Harrow, C., Lees, K.R. and Walters, M. (2009) The effect of allopurinol on the cerebral vasculature of patients with subcortical stroke; a randomized trial. British Journal of Clinical Pharmacology, 68(5), pp. 662-668. (doi:10.1111/j.1365-2125.2009.03497.x)

Full text not currently available from Enlighten.

Abstract

AIMS: New preventative strategies for stroke are required. One promising strategy is uric acid reduction and xanthine oxidase inhibition with allopurinol. We sought to investigate whether allopurinol improves cerebrovascular reactivity (CVR) following subcortical stroke. METHODS: We performed a randomized, double-blind, controlled study to investigate the effect of a 3-month course of 300 mg allopurinol once daily vs. placebo on CVR in individuals with recent (within 6 months) subcortical stroke. Participants were randomized on a 1 : 1 basis. CVR was defined as the percentage change in middle cerebral artery flow velocity following an intravenous injection of 15 mg kg−1 of acetazolamide. Our primary end-point was the CVR difference between baseline and 3 months. Secondary end-points included measures of peripheral vascular reactivity and blood markers of inflammation and endothelial activation. RESULTS: We enrolled 50 participants; 45 completed the protocol. Baseline serum urate was 0.35 mmol l−1 (SD 0.1) and 0.34 mmol l−1 (SD 0.1) in the allopurinol and placebo groups, respectively. There were no serious adverse events related to treatment. CVR did not change following treatment with allopurinol [median CVR change 0.89% after allopurinol (n= 20) and −0.68% after placebo (n= 25); 95% confidence interval for estimated difference in medians −13.4, 25.5, P= 0.64]. Urate was significantly lowered by allopurinol but no change in other secondary end-points was seen. CONCLUSION: Xanthine oxidase inhibition with allopurinol has previously been shown to improve cerebrovascular function, but no benefit was seen in this study. It may therefore be that previous encouraging findings will not translate into important clinical benefits.

Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Lees, Professor Kennedy and Quinn, Dr Terence and Dawson, Professor Jesse and Walters, Professor Matthew
Authors: Dawson, J., Quinn, T.J., Harrow, C., Lees, K.R., and Walters, M.
College/School:College of Medical Veterinary and Life Sciences > Institute of Cardiovascular and Medical Sciences
Journal Name:British Journal of Clinical Pharmacology
ISSN:0306-5251
Published Online:21 July 2009
Related URLs:

University Staff: Request a correction | Enlighten Editors: Update this record