Stroke. 2006 Jun;37(6):1427-31. Epub
2006 Apr 27.
Bushnell CD, Griffin J, Newby LK, Goldstein LB, Mahaffey
KW, Graffagnino CA, Harrington RA, White HD, Simes RJ, Califf
RM, Topol EJ, Easton JD.
Center for Cerebrovascular Disease, Duke University Medical
Center, Durham, NC 27710, USA.
BACKGROUND AND PURPOSE: Although statins reduce
the risk of stroke in patients with coronary heart disease, possible
differing effects of statins on stroke outcomes based on sex remain
uncertain. We investigated the relationships between statin use
and sex-specific stroke incidence, severity, and mortality.
METHODS: Data from 3 trials of oral glycoprotein
IIb/IIIa inhibitors (first and second Sibrafiban versus aspirin
to Yield Maximum Protection from ischemic Heart events postacute
cOroNary sYndromes [SYMPHONY] and Blockade of the glycoprotein
IIb/IIIa Receptor to Avoid Vascular Occlusion [BRAVO]) were pooled
and stroke outcomes compared among 8191 baseline statin users
versus 14,752 nonusers. Time-to-event data were modeled with proportional
hazards regression. Stroke severity was assessed retrospectively
with the Canadian Neurological Scale (CNS) based on records with
scoreable neurological examinations.
RESULTS: A total of 217 subjects had strokes
(0.95%). Statin users had a lower risk of stroke in unadjusted
(hazard ratio [HR], 0.69; 95% CI, 0.51 to 0.92) and risk-adjusted
models (HR, 0.72; 95% CI, 0.53 to 0.97). There was no difference
in stroke mortality with statin use (P=0.8). CNS scores could
be assigned to 106 of the subjects, with no difference in severity
among statin users and nonusers (median CNS=10.5 in users versus
CNS=9.75 in nonusers; P=0.14). Women had more severe strokes than
men (median CNS=10.5 in men versus 9.5 in women; Poisson regression
P=0.035). Women had more severe strokes after adjustment for statin
use (P=0.03) and the combination of statin use, atrial fibrillation,
and age (P=0.03).
CONCLUSIONS: In patients included in these clinical
trials of oral glycoprotein IIb/IIIa inhibitors, statin use is
associated with a reduced risk of stroke but not severity or mortality.
Women had more severe strokes than men, a difference that was
not explained by baseline characteristics or statin use.
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