Department of Neurology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Republic of Korea.
Neuromuscul Disord. 2012 May;22(5):394-400. doi: 10.1016/j.nmd.2011.11.006. Epub 2012 Jan 20.
Precise topographic localization, predominance in males mostly of Asian origin, and existence of some familial cases suggest a genetic background for monomelic amyotrophy. To identify susceptibility genes for monomelic amyotrophy, we performed whole-exome sequencing of four unrelated patients with monomelic amyotrophy and detected a total of 45 novel nonsynonymous single-nucleotide polymorphisms as unique variants to monomelic amyotrophy compared to control exomes. Genetic association analysis showed significant association with monomelic amyotrophy in the Gly668Ser variant of the KIAA1377 gene (odds ratio=4.62, P-value=0.0040) and the Pro1794Leu variant of the C5orf42 gene (odds ratio=4.63, P-value=0.0040). Moreover, the combination of two variants increased the risk of monomelic amyotrophy (P=1.4×10(-5), OR=61.69, 95% confidence interval=9.62-394.94, in case of combination of two heterozygotes). These data suggest that KIAA1377 and C5orf42 synergistically play a role as susceptibility genes for monomelic amyotrophy.
精确的局部定位、主要发生在亚洲男性以及一些家族病例表明,先天性肌萎缩症存在遗传背景。为了确定先天性肌萎缩症的易感基因,我们对 4 名先天性肌萎缩症患者进行了全外显子组测序,与对照外显子组相比,共检测到 45 种独特的非同义单核苷酸多态性,这些多态性是先天性肌萎缩症所特有的。遗传关联分析显示,KIAA1377 基因的 Gly668Ser 变异体(优势比=4.62,P 值=0.0040)和 C5orf42 基因的 Pro1794Leu 变异体与先天性肌萎缩症显著相关(优势比=4.63,P 值=0.0040)。此外,两种变异体的组合增加了先天性肌萎缩症的风险(P=1.4×10(-5),OR=61.69,95%置信区间=9.62-394.94,在两种杂合子的情况下)。这些数据表明,KIAA1377 和 C5orf42 协同作用,作为先天性肌萎缩症的易感基因。