Literature DB >> 33618928

Genetic epidemiology of familial ALS in Brazil.

João Pedro Nunes Gonçalves1, Tauana Bernardes Leoni1, Melina Pazian Martins1, Thiago Mazzo Peluzzo1, Mario Emílio T Dourado2, Jonas Alex M Saute3, Anna Paula Paranhos Miranda Covaleski4, Acary Souza Bulle de Oliveira5, Rinaldo Claudino6, Wilson Marques7, Anamarli Nucci1, Marcondes C França8.   

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.
Copyright © 2021 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Amyotrophic lateral sclerosis; Genetics; VAPB; Whole exome sequencing

Mesh:

Substances:

Year:  2021        PMID: 33618928     DOI: 10.1016/j.neurobiolaging.2021.01.007

Source DB:  PubMed          Journal:  Neurobiol Aging        ISSN: 0197-4580            Impact factor:   4.673


  3 in total

Review 1.  VAP Proteins - From Organelle Tethers to Pathogenic Host Interactors and Their Role in Neuronal Disease.

Authors:  Suzan Kors; Joseph L Costello; Michael Schrader
Journal:  Front Cell Dev Biol       Date:  2022-06-08

2.  Phenotype of VCP Mutations in Chinese Amyotrophic Lateral Sclerosis Patients.

Authors:  Shu-Yan Feng; Han Lin; Chun-Hui Che; Hua-Pin Huang; Chang-Yun Liu; Zhang-Yu Zou
Journal:  Front Neurol       Date:  2022-02-07       Impact factor: 4.003

3.  ANXA11 mutations are associated with amyotrophic lateral sclerosis-frontotemporal dementia.

Authors:  Yu Wang; Xiaohui Duan; Xiao Zhou; Renbin Wang; Xiangfei Zhang; Zhenhua Cao; Xiaoxia Wang; Zhi Zhou; Yu Sun; Dantao Peng
Journal:  Front Neurol       Date:  2022-09-26       Impact factor: 4.086

  3 in total

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