OBJECTIVE: TO assess the relative antiaggregatory ability of aspirin o
n platelets of smoking and nonsmoking healthy volunteers. DESIGN: Pros
pective, randomized, crossover study. SETTING: Tertiary-care teaching
institution. SUBJECTS: Eighteen healthy smoking and nonsmoking male vo
lunteers. INTERVENTIONS: Each subject received aspirin 325 mg or ticlo
pidine 250 mg bid as an active control for 7 days in a crossover manne
r separated by a 1-month washout period. Whole blood platelet aggregat
ion was measured on four occasions, twice at baseline and once after e
ach drug treatment. OUTCOME MEASUREMENT: Whole blood ex vivo platelet
aggregation in terms of impedance (Omega) and adenosine triphosphate (
ATP) release (nmol), as assessed using Lumi-aggregometry. RESULTS: Asp
irin was associated with significantly less ATP release in both smoker
s (p = 0.01) and nonsmokers (p = 0.003). No significant differences in
platelet aggregation were found between smokers and nonsmokers at bas
eline or with any treatment phases. Sixty-seven percent and 17% of vol
unteers receiving ticlopidine and aspirin, respectively, reported adve
rse effects. CONCLUSIONS: Twice-daily administration of aspirin for 7
days to healthy volunteers was well tolerated and also reduced platele
t aggregation significantly regardless of smoking status.