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Cited 8 time in webofscience Cited 7 time in scopus
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Determinants of Basal Collaterals in Moyamoya Disease: Clinical and Genetic Factors

Authors
Chung, JW[Chung, Jong-Won]Kim, SJ[Kim, Suk Jae]Bang, OY[Bang, Oh Young]Kim, KH[Kim, Kun Ha]Ki, CS[Ki, Chang-Seok]Jeon, P[Jeon, Pyeong]Yeon, JY[Yeon, Je Young]Kim, JS[Kim, Jong-Soo]Hong, SC[Hong, Seung Chyul]Shin, HJ[Shin, Hyung Jin]
Issue Date
2016
Publisher
KARGER
Keywords
Genetics; Intracranial stenosis; Collaterals; Moyamoya; Stroke
Citation
EUROPEAN NEUROLOGY, v.75, no.3-4, pp.178 - 185
Indexed
SCIE
SCOPUS
Journal Title
EUROPEAN NEUROLOGY
Volume
75
Number
3-4
Start Page
178
End Page
185
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/41725
DOI
10.1159/000445348
ISSN
0014-3022
Abstract
Background/Aims: To enable the diagnosis of moyamoya disease (MMD), detection of distal internal carotid artery stenosis and hazy network of basal collaterals (BCs) are required. This study aimed at evaluating the factors that could determine the degree of BCs in patients with angiographically confirmed MMD. Methods: We analyzed 146 consecutive patients with MMD (age 26.2 +/- 19.6, range 1-75). The degree of BCs (%) was measured based on conventional angiography. Factors associated with the degree of BCs, including clinico-radiological and genetic factors (p.Arg4810Lys variant), were analyzed. Results:The degree of BCs varied among MMD patients and significantly decreased with an increase in the age of diagnosis of MMD (coefficient -1.55; p < 0.001). Although the degree of BC development depends on the MMD stage (Suzuki stage), it is less prominent in adult-onset (>18 years) MMD compared to childhood MMD. The presence of p.Arg4810Lys variant, types of MMD (bilateral vs. uni-lateral) and stroke (ischemic, hemorrhagic, or asymptomatic), shrinkage (outer diameter) of intracranial vessels, external carotid collateral status, and cortical neovascularization were not associated with the degree of BCs. Conclusion: Although prominent BCs are required for diagnosis of MMD, BCs are decreased with aging, suggesting that angiogenic capacity is altered in adult onset MMD compared to childhood MMD. (C) 2016 S. Karger AG, Basel
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