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Effect of cilostazol on cerebral arteries in secondary prevention of ischemic stroke
Jian-Jun Guo1, En Xu, Qing-Yuan Lin
1Department of Neurology, the 2nd Affiliated Hospital of Guangzhou Medical College, Guangzhou, China.
Insights
Cilostazol shows comparable effectiveness to aspirin in preventing cerebral artery issues after ischemic stroke. It also demonstrated fewer bleeding side effects and improved blood flow, suggesting it is a safer alternative.
Area of Science:
- Neuroscience
- Cardiovascular Medicine
- Pharmacology
Background:
- Secondary prevention of ischemic stroke is crucial for reducing recurrence and improving patient outcomes.
- Cerebral artery condition and cerebrovascular blood flow are key indicators of stroke risk.
- Aspirin is a standard treatment, but alternative agents are being investigated for enhanced efficacy and safety.
Purpose of the Study:
- To compare the effects of cilostazol versus aspirin on cerebral arteries and cerebrovascular blood flow.
- To evaluate the efficacy and safety of cilostazol in secondary prevention of ischemic stroke.
Main Methods:
- Sixty-eight patients with recent ischemic stroke were randomized into cilostazol or aspirin groups.
- Cerebrovascular condition was assessed using magnetic resonance angiography (MRA) and transcranial Doppler ultrasonography (TCD).
- Assessments were conducted at baseline and after 12 months of medication.
Main Results:
- Cilostazol group had fewer bleeding events (0 vs. 5 in aspirin group, P<0.05).
- Cilostazol significantly increased systolic peak flow velocity in cerebral arteries (42.9% vs. 27.5% for aspirin, P=0.04).
- Both drugs showed comparable effects on preventing the aggravation of cerebral arteries, with cilostazol demonstrating a trend towards less aggravation via TCD.
Conclusions:
- Cilostazol is as effective as aspirin in preventing cerebral artery aggravation in secondary stroke prevention.
- Cilostazol presents a safer profile with significantly lower bleeding frequency.
- The improvement in cerebral blood flow velocity with cilostazol may enhance perfusion in ischemic areas.
Objective:
To compare the effects of cilostazol on cerebral arteries and cerebrovascular blood flow in secondary prevention of ischemic stroke, with those of aspirin.
Methods:
Sixty-eight patients who had ischemic stroke during the recent 1-6 months were recruited and randomized into cilostazol or aspirin group. Cerebrovascular condition was assessed by magnetic resonance angiography (MRA) and transcranial doppler ultrasonography (TCD) at the beginning of the study and after 12-month medication.
Results:
During the clinical follow-up, ischemic stroke recurred in 2 patients in cilostazol group, while in aspirin group, one case of ischemic stroke recurrence and one case of acute myocardial infarction were found. MRA revealed that in aspirin group, the percentages of patients experiencing aggravation and attenuation of cerebrovascular condition were 3.3% and 6.7%, respectively, while in aspirin group, they were 3.3% and 10%, respectively. Moreover, TCD revealed that 26.9% of the patients in aspirin group and 14.3% of the patients in cilostazol group experienced aggravation of cerebrovascular condition. However, the systolic peak flow velocity of the previously abnormal arteries increased by 42.9% after 12-month medication of cilostazol, which was significantly higher than that after aspirin medication (27.5%) (P = 0.04). Furthermore, as a major side effect of antiplatelet therapy, the frequency of bleeding was much less in cilostazol group (0 case in cilostazol group vs 5 in aspirin, P< 0.05).
Conclusion:
Cilostazol is as effective as aspirin in preventing the aggravation of cerebral arteries in secondary prevention of ischemic stroke. Besides, it is more safe. Cilostazol can increase the systolic peak flow velocity of cerebral arteries, which may improve the blood supply of focal ischemia.
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