Clinical course of asymptomatic adult moyamoya disease

Kyung-Il Jo1, Je Young Yeon, Seung-Chyul Hong

  • 1Department of Neurosurgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

Abstract

Insights

Asymptomatic moyamoya disease (MMD) in adults is not stable, with some patients experiencing transient ischemic attacks. However, stroke rates were low, suggesting antiplatelet therapy and risk factor control are appropriate initial treatments.

Area of Science:

  • Neurology
  • Vascular Neurology
  • Neuroimaging

Background:

  • Increasing prevalence of asymptomatic moyamoya disease (MMD) due to regular check-ups.
  • Unclear definition and clinical features of asymptomatic MMD hinder management guidelines.
  • Need to define and clarify clinical characteristics of adult asymptomatic MMD.

Purpose of the Study:

  • To define asymptomatic moyamoya disease (MMD) in adults.
  • To clarify the clinical characteristics of asymptomatic MMD.
  • To evaluate the clinical course and identify prognostic factors.

Main Methods:

  • Retrospective cohort study of 40 adult MMD patients (1995-2010).
  • Defined asymptomatic MMD as no infarction or ischemia on MRI.
  • Evaluated demographic, radiological, and clinical findings; used log-rank, Pearson's, and Mann-Whitney U tests.

Main Results:

  • 19% and 22% showed decreased basal and acetazolamide stress brain perfusion, respectively.
  • Transient ischemic attack occurred in 3 non-surgically treated patients, linked to decreased vascular reserve and smoking.
  • Radiological progression occurred in 3 patients, related to hypertension; no strokes were reported.

Conclusions:

  • Asymptomatic MMD in adults is not a stable condition.
  • Low stroke rate (0%) observed, lower than previous reports.
  • Antiplatelet medication and risk factor control are suitable initial treatments for patients with normal cerebrovascular reserve.

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