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在中国东部肌萎缩侧索硬化症患者中,ATXN2基因中的中等长度聚谷氨酰胺可能是一个风险因素。

Intermediate-length polyglutamine in ATXN2 is a possible risk factor among Eastern Chinese patients with amyotrophic lateral sclerosis.

作者信息

Lu Hai-Peng, Gan Shi-Rui, Chen Sheng, Li Hong-Fu, Liu Zhi-Jun, Ni Wang, Wang Ning, Wu Zhi-Ying

机构信息

Department of Neurology and Institute of Neurology, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China; Department of Neurology and Institute of Neurology, First Affiliated Hospital, Fujian Medical University, Fuzhou, China; Department of Neurology, Jinhua Hospital, Zhejiang University, Jinhua, China.

Department of Neurology and Institute of Neurology, First Affiliated Hospital, Fujian Medical University, Fuzhou, China.

出版信息

Neurobiol Aging. 2015 Mar;36(3):1603.e11-4. doi: 10.1016/j.neurobiolaging.2014.10.015. Epub 2014 Oct 16.

Abstract

An effective treatment for amyotrophic lateral sclerosis (ALS) has not yet been found because the pathogenesis of this fatal disease is not well understood. A number of previous studies demonstrated that intermediate-length polyglutamine repeats within the ataxin-2 gene (ATXN2) might be a risk factor among patients with ALS in Western countries. Here, we aim to determine whether this sequence is a risk factor in Eastern Chinese ALS patients. Therefore, 379 unrelated sporadic ALS patients, 15 unrelated familial ALS patients, and 900 neurologically normal controls were studied. The ATXN2 CAG repeats were amplified using polymerase chain reaction. The products were separated on an 8% polyacrylamide gel and confirmed using Sanger sequencing. The results were evaluated using SPSS 17.0. We found that ATXN2 intermediate-length polyglutamine expansions greater than 24 and 27 repeats were associated with sporadic ALS. Our finding supports the hypothesis that ATXN2 plays an important role in the pathogenesis of ALS.

摘要

由于这种致命疾病的发病机制尚未完全明确,所以尚未找到治疗肌萎缩侧索硬化症(ALS)的有效方法。此前的多项研究表明,ataxin-2基因(ATXN2)内的中等长度聚谷氨酰胺重复序列可能是西方国家ALS患者的一个风险因素。在此,我们旨在确定该序列在中国东部ALS患者中是否为风险因素。因此,我们研究了379例无亲缘关系的散发性ALS患者、15例无亲缘关系的家族性ALS患者以及900例神经系统正常的对照者。采用聚合酶链反应扩增ATXN2 CAG重复序列。产物在8%聚丙烯酰胺凝胶上进行分离,并用桑格测序法进行确认。结果使用SPSS 17.0进行评估。我们发现,ATXN2中等长度聚谷氨酰胺重复序列大于24次和27次与散发性ALS相关。我们的发现支持了ATXN2在ALS发病机制中起重要作用这一假说。

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