Key result
Smoking was associated with a significantly lower incidence of clopidogrel resistance compared to non-smokers (12.9% vs 25.9%, p=0.033) in patients with non-cardiogenic ischemic stroke.
Why the study?
Does smoking improve responsiveness to clopidogrel in non-cardiogenic ischemic stroke patients?
Observational (n=209)
No
Does smoking improve responsiveness to clopidogrel in non-cardiogenic ischemic stroke patients?
Smoking is associated with enhanced clopidogrel responsiveness and a lower incidence of clopidogrel resistance in patients with non-cardiogenic ischemic stroke.
No change to clopidogrel use or smoking cessation advice; leaves open causal mechanisms in non-cardiogenic stroke.
OBJECTIVE: Clopidogrel is used to prevent the recurrence of non-cardiogenic ischemic stroke, but individual responsiveness to the drug varies. Moreover, it is known that smoking, which is a risk factor for ischemic stroke, affects the drug's pharmacokinetics. The objective of the present study was to investigate a possible relationship between smoking and responsiveness to clopidogrel in non-cardiogenic ischemic stroke patients. METHODS: The study involved 209 non-cardiogenic ischemic stroke patients who were administered oral clopidogrel at a dosage of 75 mg/day for at least 1 week. Platelet aggregation in response to adenosine diphosphate (20 μM) was measured in each patient using the VerifyNow P2Y12 Assay. Platelet aggregation and the incidence of resistance to clopidogrel were compared between a smokers group (70 patients) and a non-smokers group (139 patients). Clopidogrel resistance was defined as a P2Y12 Reaction Units (PRU) value >230 and/or % inhibition <20%. RESULTS: The mean PRU was 128.3±85.5 in the smokers group and 167.7±86.6 in the non-smokers group (p=0.002). The incidence of PRU >230 was 12.9% (9 patients) in the smokers group and 25.9% (36 patients) in the non-smokers group (p=0.033). The mean % inhibition was 48.6±30.7% in the smokers group and 36.9±27.6% in the non-smokers group (p=0.009). The incidence of patients with % inhibition <20% was 24.3% (17 patients) in the smokers group and 34.5% (48 patients) in the non-smokers group (p=0.155). CONCLUSION: The incidence of clopidogrel resistance was lower in the non-cardiogenic ischemic stroke patients who were smokers, thus indicating that these patients' responsiveness to this drug may be enhanced.
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Maruyama et al. (2014) conducted an observational in Non-cardiogenic ischemic stroke (n=209). Smoking vs. Non-smokers was evaluated on Incidence of clopidogrel resistance (defined as PRU > 230) (p=0.033). Smoking was associated with a significantly lower incidence of clopidogrel resistance compared to non-smokers (12.9% vs 25.9%, p=0.033) in patients with non-cardiogenic ischemic stroke.
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