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May 02, 2023; 100 (18) Research Article

Characteristics and Clinical Implication of White Matter Lesions in Patients With Adult Moyamoya Disease

View ORCID ProfileWookjin Yang, Keun-Hwa Jung, Dong-Wan Kang, Eung-Joon Lee, View ORCID ProfileHan-Yeong Jeong, Matthew Chung, Youngjoon Kim, Jiyeon Ha, Jeong-Min Kim, Seung-Hoon Lee
First published March 6, 2023, DOI: https://doi.org/10.1212/WNL.0000000000207130
Wookjin Yang
From the Department of Neurology, Seoul National University Hospital, Korea.
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Keun-Hwa Jung
From the Department of Neurology, Seoul National University Hospital, Korea.
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Dong-Wan Kang
From the Department of Neurology, Seoul National University Hospital, Korea.
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Eung-Joon Lee
From the Department of Neurology, Seoul National University Hospital, Korea.
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Han-Yeong Jeong
From the Department of Neurology, Seoul National University Hospital, Korea.
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Matthew Chung
From the Department of Neurology, Seoul National University Hospital, Korea.
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Youngjoon Kim
From the Department of Neurology, Seoul National University Hospital, Korea.
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Jiyeon Ha
From the Department of Neurology, Seoul National University Hospital, Korea.
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Jeong-Min Kim
From the Department of Neurology, Seoul National University Hospital, Korea.
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Seung-Hoon Lee
From the Department of Neurology, Seoul National University Hospital, Korea.
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Characteristics and Clinical Implication of White Matter Lesions in Patients With Adult Moyamoya Disease
Wookjin Yang, Keun-Hwa Jung, Dong-Wan Kang, Eung-Joon Lee, Han-Yeong Jeong, Matthew Chung, Youngjoon Kim, Jiyeon Ha, Jeong-Min Kim, Seung-Hoon Lee
Neurology May 2023, 100 (18) e1912-e1921; DOI: 10.1212/WNL.0000000000207130

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Abstract

Background and Objectives White matter hyperintensities (WMHs) are reportedly increased in moyamoya disease (MMD); however, their clinical importance is not well-established owing to their pathophysiologic heterogeneity by distribution. This study aimed to evaluate the burden and pattern of WMHs and its clinical implications in the MMD trajectory.

Methods Adult patients with MMD without significant structural lesions were 1:1 propensity score-matched with healthy controls for sex and vascular risk factors. The total, periventricular, and subcortical WMH volumes were segmented and quantified fully automatically. WMH volumes were detrended by age and compared between the 2 groups. MMD severity based on Suzuki stage and future ischemic events were assessed for their association with WMH volumes.

Results A total of 161 pairs of patients with MMD and controls were analyzed. MMD significantly correlated with increased total WMH volume (B [standard error], 0.126 [0.030]; p < 0.001), periventricular WMH volume (0.114 [0.027]; p < 0.001), and periventricular-to-subcortical ratio (0.090 [0.034]; p = 0.009). In the MMD subgroup (n = 187), advanced MMD had an independent association with the total WMH volume (0.120 [0.035]; p < 0.001), periventricular WMH volume (0.110 [0.031]; p < 0.001), and periventricular-to-subcortical ratio (0.139 [0.038]; p < 0.001). Periventricular WMH volume (adjusted hazard ratio [95% confidence interval], 5.12 [1.26–20.79]) and periventricular-to-subcortical ratio (3.80 [1.51–9.56]) were associated with future ischemic events in patients with medically followed up MMD. However, no demonstrable association was found between subcortical WMH volume and MMD, MMD severity, or future ischemic events.

Discussion Periventricular WMHs, but not subcortical WMHs, may represent the main pathophysiology of MMD. Periventricular WMHs may be used as a marker for ischemic vulnerability in patients with MMD.

Glossary

FSPGR=
fast spoiled gradient echo;
MMD=
moyamoya disease;
MPRAGE=
magnetization prepared rapid gradient echo;
TFE=
turbo field echo;
TIA=
transient ischemic attack;
WMH=
White matter hyperintensities

Footnotes

  • Go to Neurology.org/N for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.

  • Submitted and externally peer reviewed. The handling editor was Editor-in-Chief José Merino, MD, MPhil, FAAN.

  • Received September 5, 2022.
  • Accepted in final form January 17, 2023.
  • © 2023 American Academy of Neurology
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