Human Leukocyte Antigen in Patients With Moyamoya Disease

Author:

Aoyagi Masaru1,Ogami Kazuo1,Matsushima Yoshiharu1,Shikata Manabu1,Yamamoto Mari1,Yamamoto Kiyotaka1

Affiliation:

1. From the Department of Neurosurgery, Tokyo Medical and Dental University, Bunkyo-ku (M.A., Y.M.), and the Department of Cell Biology, Tokyo Metropolitan Institute of Gerontology, Itabashi-ku (M.A., K.O., M.S., M.Y., K.Y.), Tokyo, Japan.

Abstract

Background and Purpose Progressive stenosis or occlusion of bilateral internal carotid arteries by fibrocellular intimal thickening results in cerebral ischemia in moyamoya disease. In an attempt to elucidate the still-unknown etiologic factors in moyamoya disease, we assessed human leukocyte antigens in patients with this disease. Methods We investigated 32 unrelated Japanese patients with moyamoya disease for typing of human leukocyte antigen A, B, C, and DR/DQ and compared the results with those from 178 unrelated control subjects. Results We found a significant association of human leukocyte antigen B51 with moyamoya disease (corrected P <.05, χ 2 test). Although no significant associations were observed in DR/DQ typing, the frequency of the B51-DR4 combination was significantly higher in moyamoya patients than in control subjects ( P <.002, Fisher’s exact test). Conclusions These findings suggest that there may be a genetic predisposition for moyamoya disease and that host factors may play a role in the development of intimal thickening in early childhood.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Advanced and Specialized Nursing,Cardiology and Cardiovascular Medicine,Neurology (clinical)

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