Prospective screening of family members with moyamoya disease patients.

BACKGROUND: Genetic factors play an important role in the pathogenesis of moyamoya disease (MMD). Previous studies concentrated on familial MMD patients. In this study, we focused on family members of sporadic MMD patients, and aimed to gain a clearer understanding of the role that genetic factors p...

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Main Authors: Cong Han, Hui Feng, Yi-Qin Han, Wei-Wei Liu, Zheng-Shan Zhang, Wei-Zhong Yang, Lian Duan
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3929504?pdf=render
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spelling doaj-b09e8c1351e34635852352e448f85d462020-11-25T01:27:33ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0192e8876510.1371/journal.pone.0088765Prospective screening of family members with moyamoya disease patients.Cong HanHui FengYi-Qin HanWei-Wei LiuZheng-Shan ZhangWei-Zhong YangLian DuanBACKGROUND: Genetic factors play an important role in the pathogenesis of moyamoya disease (MMD). Previous studies concentrated on familial MMD patients. In this study, we focused on family members of sporadic MMD patients, and aimed to gain a clearer understanding of the role that genetic factors play in MMD. METHODS: The immediate family members of MMD patients were initially screened by transcranial Doppler sonography (TCD) and positive cases were verified by magnetic resonance angiography (MRA). RESULTS: From July 2011 to March 2013, there were 527 MMD patients managed in our hospital, including 38 familial MMD cases. In this study, 285 immediate family members of 245 sporadic MMD patients were screened. Another 41 cases of familial MMD cases were identified, which included 21 family members and 20 corresponding sporadic MMD patients who had family members confirmed positive with MMD. As a result, the proportion of familial MMD patients increased from 7% (38/527) to 15% (79/527) in this period. For the main segments of the circle of Willis, Kappa values between TCD and MRA for the anterior cerebral arteries, middle cerebral arteries and posterior cerebral arteries were 0.91, 0.72, and 0.47, respectively. Familial cases confirmed by our screening showed a significantly higher percentage of asymptomatic patients (57%) compared with 9% from the control group who had a clear family history before. CONCLUSIONS: Familial MMD patients may account for a higher percentage among all cases than previously thought. Some family members of MMD patients may also have MMD, but not have any obvious symptoms. Routine screening should be implemented for all family members of MMD patients to improve the detection rate for this part of the patient base. TCD has a high diagnostic agreement with MRA for MMD. TCD may be the preferred choice for screening because it is inexpensive and safe.http://europepmc.org/articles/PMC3929504?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Cong Han
Hui Feng
Yi-Qin Han
Wei-Wei Liu
Zheng-Shan Zhang
Wei-Zhong Yang
Lian Duan
spellingShingle Cong Han
Hui Feng
Yi-Qin Han
Wei-Wei Liu
Zheng-Shan Zhang
Wei-Zhong Yang
Lian Duan
Prospective screening of family members with moyamoya disease patients.
PLoS ONE
author_facet Cong Han
Hui Feng
Yi-Qin Han
Wei-Wei Liu
Zheng-Shan Zhang
Wei-Zhong Yang
Lian Duan
author_sort Cong Han
title Prospective screening of family members with moyamoya disease patients.
title_short Prospective screening of family members with moyamoya disease patients.
title_full Prospective screening of family members with moyamoya disease patients.
title_fullStr Prospective screening of family members with moyamoya disease patients.
title_full_unstemmed Prospective screening of family members with moyamoya disease patients.
title_sort prospective screening of family members with moyamoya disease patients.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description BACKGROUND: Genetic factors play an important role in the pathogenesis of moyamoya disease (MMD). Previous studies concentrated on familial MMD patients. In this study, we focused on family members of sporadic MMD patients, and aimed to gain a clearer understanding of the role that genetic factors play in MMD. METHODS: The immediate family members of MMD patients were initially screened by transcranial Doppler sonography (TCD) and positive cases were verified by magnetic resonance angiography (MRA). RESULTS: From July 2011 to March 2013, there were 527 MMD patients managed in our hospital, including 38 familial MMD cases. In this study, 285 immediate family members of 245 sporadic MMD patients were screened. Another 41 cases of familial MMD cases were identified, which included 21 family members and 20 corresponding sporadic MMD patients who had family members confirmed positive with MMD. As a result, the proportion of familial MMD patients increased from 7% (38/527) to 15% (79/527) in this period. For the main segments of the circle of Willis, Kappa values between TCD and MRA for the anterior cerebral arteries, middle cerebral arteries and posterior cerebral arteries were 0.91, 0.72, and 0.47, respectively. Familial cases confirmed by our screening showed a significantly higher percentage of asymptomatic patients (57%) compared with 9% from the control group who had a clear family history before. CONCLUSIONS: Familial MMD patients may account for a higher percentage among all cases than previously thought. Some family members of MMD patients may also have MMD, but not have any obvious symptoms. Routine screening should be implemented for all family members of MMD patients to improve the detection rate for this part of the patient base. TCD has a high diagnostic agreement with MRA for MMD. TCD may be the preferred choice for screening because it is inexpensive and safe.
url http://europepmc.org/articles/PMC3929504?pdf=render
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