Key result
Cilostazol is associated with middle cerebral artery stenosis improvement in ~26% of patients at 12 months.
Why the study?
The effectiveness of cilostazol on intracranial arterial stenosis and its impact on cerebral blood flow were evaluated using MRA and SPECT.
Cohort (n=20)
No
Cilostazol may improve select MCA stenoses and perfusion; hypothesis-generating and requires randomized confirmation before practice change.
BACKGROUND: To evaluate the effectiveness of cilostazol in patients with intracranial arterial stenosis, we used magnetic resonance angiography (MRA). The drug's effect on the cerebral blood flow (CBF) was examined by single photon emission computed tomography (SPECT). METHODS: In this retrospective study, we evaluated the clinical outcomes of 20 patients with stenosis in the M1 segment of the middle cerebral artery (MCA) who had suffered ischemic stroke within 12 weeks or manifested asymptomatic stenosis exceeding 50%. All patients received cilostazol (100 mg twice daily). MRA and SPECT (at rest and after acetazolamide challenge) studies were performed before and 6 and 12 months after the start of cilostazol treatment. RESULTS: In 5 patients the stenotic lesion showed improvement on MRA. Mean stenosis before cilostazol therapy was 71.7 ± 4.9%, which improved to 39.0 ± 3.2% at 6 months and to 27.2 ± 2.8% at 12 months. SPECT study showed that CBF was improved in 3 patients; in one there was improvement at rest and the other 2 manifested improvement upon acetazolamide challenge. CONCLUSIONS: Cilostazol had a remodeling effect on stenotic lesions due to arteriosclerotic changes and improved CBF in some patients.
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Kai et al. (2011) conducted a cohort in Intracranial arterial stenosis (M1 segment of middle cerebral artery) (n=20). Cilostazol was evaluated on Improvement in M1 segment stenosis to less than 50% at 12 months. Cilostazol treatment for 12 months improved M1 segment middle cerebral artery stenosis in 26.3% (5 of 19) of patients, with concurrent improvements in cerebral blood flow observed in responders.
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