Ikeuchi T, Takano H, Koide R, Horikawa Y, Honma Y, Onishi Y, Igarashi S, Tanaka H, Nakao N, Sahashi K, Tsukagoshi H, Inoue K, Takahashi H, Tsuji S
Department of Neurology, Brain Research Institute, Niigata University, Japan.
Ann Neurol. 1997 Dec;42(6):879-84. doi: 10.1002/ana.410420609.
Autosomal dominant spinocerebellar ataxias (SCAs) are clinically and genetically a heterogeneous group of neurodegenerative disorders. Recently, mild CAG repeat expansion in the alpha1A voltage-dependent calcium channel gene has been found to be associated with a type of autosomal dominant SCA (SCA6). We analyzed 98 Japanese families with autosomal dominant SCAs, for whom CAG repeat expansions of the SCA1, SCA2, Machado-Joseph disease/SCA3, and dentatorubral-pallidoluysian atrophy genes were excluded, and 5 apparently sporadic cases of cortical cerebellar atrophy. The diagnosis of SCA6 was confirmed in 30 families (31%) comprising 47 affected individuals and 1 sporadic case. The size of expanded CAG repeats ranged from 21 to 26 repeat units and was found to be correlated inversely with age at onset. We identified 2 SCA6 patients homozygous for expanded CAG repeats, whose ages at onset were earlier than the 95% lower confidence level, suggesting the presence of a gene dosage effect of expanded CAG repeat. Ataxia is the most common initial symptom found in 45 of the 48 patients. Patients with a prolonged disease course showed other accompanying clinical features including dystonic postures, involuntary movements, and abnormalities in tendon reflexes.
常染色体显性遗传性脊髓小脑共济失调(SCAs)在临床和遗传学上是一组异质性神经退行性疾病。最近,已发现α1A电压依赖性钙通道基因中轻度的CAG重复序列扩增与一种常染色体显性遗传性SCA(SCA6)相关。我们分析了98个常染色体显性遗传性SCAs的日裔家族,这些家族排除了SCA1、SCA2、马查多-约瑟夫病/SCA3和齿状核红核苍白球路易体萎缩基因的CAG重复序列扩增情况,以及5例明显散发的皮质小脑萎缩病例。在30个家族(31%)中确诊为SCA6,包括47例受累个体和1例散发病例。扩增的CAG重复序列大小范围为21至26个重复单位,且发现与发病年龄呈负相关。我们鉴定出2例CAG重复序列扩增纯合的SCA6患者,其发病年龄早于95%的低置信水平,提示存在扩增的CAG重复序列的基因剂量效应。共济失调是48例患者中45例最常见的初始症状。病程较长的患者表现出其他伴随的临床特征,包括肌张力障碍姿势、不自主运动和腱反射异常。