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韩国人群烟雾病型脑血管疾病的全基因组研究。

A genome-wide study of moyamoya-type cerebrovascular disease in the korean population.

作者信息

Joo Sung-Pil, Kim Tae Sun, Lee Il-Kwon, Kim Joon-Tae, Park Man-Seok, Cho Ki-Hyun

机构信息

Department of Neurosurgery, Chonnam National University Hospital & Medical School, Gwangju, Korea.

出版信息

J Korean Neurosurg Soc. 2011 Dec;50(6):486-91. doi: 10.3340/jkns.2011.50.6.486. Epub 2011 Dec 31.

Abstract

OBJECTIVE

Structural genetic variation, including copy-number variation (CNV), constitutes a substantial fraction of total genetic variability, and the importance of structural variants in modulating susceptibility is increasingly being recognized. CNV can change biological function and contribute to pathophysiological conditions of human disease. Its relationship with common, complex human disease in particular is not fully understood. Here, we searched the human genome to identify copy number variants that predispose to moya-moya type cerebrovascular disease.

METHODS

We retrospectively analyzed patients who had unilateral or bilateral steno-occlusive lesions at the cerebral artery from March, 2007, to September, 2009. For the 20 subjects, including patients with moyamoya type pathologies and three normal healthy controls, we divided the subjects into 4 groups : typical moyamoya (n=6), unilateral moyamoya (n=9), progression unilateral to typical moyamoya (n=2) and non-moyamoya (n=3). Fragmented DNA was hybridized on Human610Quad v1.0 DNA analysis BeadChips (Illumina). Data analysis was performed with GenomeStudio v2009.1, Genotyping 1.1.9, cnvPartition_v2.3.4 software. Overall call rates were more than 99.8%.

RESULTS

In total, 1258 CNVs were identified across the whole genome. The average number of CNV was 45.55 per subject (CNV region was 45.4). The gain/loss of CNV was 52/249, having 4.7 fold higher frequencies in loss calls. The total CNV size was 904,657,868, and average size was 993,038. The largest portion of CNVs (613 calls) were 1M-10M in length. Interestingly, significant association between unilateral moyamoya disease (MMD) and progression of unilateral to typical moyamoya was observed.

CONCLUSION

Significant association between unilateral MMD and progression of unilateral to typical moyamoya was observed. The finding was confirmed again with clustering analysis. These data demonstrate that certain CNV associate with moyamoya-type cerebrovascular disease.

摘要

目的

结构基因变异,包括拷贝数变异(CNV),构成了总遗传变异的很大一部分,并且结构变异在调节易感性方面的重要性日益得到认可。CNV可改变生物学功能并导致人类疾病的病理生理状况。其与常见的复杂人类疾病的关系,尤其是尚未完全了解。在此,我们搜索人类基因组以鉴定易患烟雾病型脑血管疾病的拷贝数变异。

方法

我们回顾性分析了2007年3月至2009年9月期间在脑动脉有单侧或双侧狭窄闭塞性病变的患者。对于这20名受试者,包括烟雾病型病变患者和三名正常健康对照,我们将受试者分为4组:典型烟雾病(n = 6)、单侧烟雾病(n = 9)、从单侧进展为典型烟雾病(n = 2)和非烟雾病(n = 3)。将片段化的DNA与Human610Quad v1.0 DNA分析微珠芯片(Illumina)杂交。使用GenomeStudio v2009.1、基因分型1.1.9、cnvPartition_v2.3.4软件进行数据分析。总体检出率超过99.8%。

结果

在整个基因组中总共鉴定出1258个CNV。每个受试者的CNV平均数量为45.55(CNV区域为45.4)。CNV的增加/减少为52/249,缺失检出频率高4.7倍。CNV的总大小为904,657,868,平均大小为993,038。最大部分的CNV(613个检出)长度为1M - 10M。有趣的是,观察到单侧烟雾病(MMD)与从单侧进展为典型烟雾病之间存在显著关联。

结论

观察到单侧MMD与从单侧进展为典型烟雾病之间存在显著关联。通过聚类分析再次证实了这一发现。这些数据表明某些CNV与烟雾病型脑血管疾病相关。

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本文引用的文献

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Autosomal dominant moyamoya disease maps to chromosome 17q25.3.常染色体显性遗传性烟雾病定位于17号染色体长臂25.3区。
Neurology. 2008 Jun 10;70(24 Pt 2):2357-63. doi: 10.1212/01.wnl.0000291012.49986.f9. Epub 2008 May 7.
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Progression of unilateral moyamoya disease: A clinical series.单侧烟雾病的进展:临床系列研究
Cerebrovasc Dis. 2006;22(2-3):109-15. doi: 10.1159/000093238. Epub 2006 May 9.

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