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巴西家族性肌萎缩侧索硬化症的遗传流行病学。

Genetic epidemiology of familial ALS in Brazil.

机构信息

Departments of Neurology and Medical Genetics, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, SP, BRAZIL.

Department of Integrative Medicine, Federal University of Rio Grande do Norte, Natal, Brazil.

出版信息

Neurobiol Aging. 2021 Jun;102:227.e1-227.e4. doi: 10.1016/j.neurobiolaging.2021.01.007. Epub 2021 Jan 22.

Abstract

Many genes associated with familial forms of the amyotrophic lateral sclerosis (fALS) have been identified in European and North American cohorts. However, little is known about the genetic bases of fALS in Latin America and Brazil, in particular. To address this question, we recruited 107 patients with fALS from 93 unrelated families from Southeastern, Southern, and Northeastern regions of the country. A 3-step diagnostic approach was used: 1) Triplet repeat primed polymerase chain reaction to search for C9orf72 expansions, then 2) fragment digestion to search for the c.166 C>T VAPB variant, and finally, 3) whole exome sequencing for those who tested negative. We identified the genetic cause for fALS in 70% of the families. VAPB and C9orf72 were the most frequent genes (30% and 22%, respectively), followed by SOD1, TARDBP, ANXA11, and FUS. Five novel variants in known ALS genes were found, including the SOD1 Val120Leu and ANXA11 Asp40Tyr, which were seen in 2 unrelated families each. In conclusion, VAPB and then C9orf72 are the genes most commonly related to fALS in Brazil.

摘要

许多与肌萎缩侧索硬化症(fALS)家族形式相关的基因已在欧洲和北美队列中被发现。然而,人们对拉丁美洲和巴西,特别是巴西的 fALS 的遗传基础知之甚少。为了解决这个问题,我们从该国东南部、南部和东北部地区的 93 个无关家庭中招募了 107 名 fALS 患者。采用了 3 步诊断方法:1)三核苷酸重复引物聚合酶链反应搜索 C9orf72 扩展,然后 2)片段消化搜索 c.166 C>T VAPB 变体,最后 3)对那些检测结果为阴性的人进行全外显子组测序。我们确定了 70%的家庭中 fALS 的遗传原因。VAPB 和 C9orf72 是最常见的基因(分别为 30%和 22%),其次是 SOD1、TARDBP、ANXA11 和 FUS。在已知的 ALS 基因中发现了 5 种新的变体,包括 SOD1 Val120Leu 和 ANXA11 Asp40Tyr,它们分别出现在 2 个无关家庭中。总之,VAPB 然后是 C9orf72 是与巴西 fALS 最相关的基因。

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