dc.contributorhttps://orcid.org/0000-0002-9462-2294
dc.creatorDourado Junior, Mário Emílio Teixeira
dc.creatorAndrade, Helen Maia Tavares de
dc.creatorCintra, Vívian Pedigone; et al.
dc.date2023-07-27T19:28:06Z
dc.date2023-07-27T19:28:06Z
dc.date2018
dc.date.accessioned2023-09-04T14:10:40Z
dc.date.available2023-09-04T14:10:40Z
dc.identifierANDRADE, Helen Maia Tavares de; CINTRA, Vívian Pedigone; ALBUQUERQUE, Milena de; PICCININ, Camila Callegari; BONADIA, Luciana Cardoso; COUTEIRO, Rafael Esteves Duarte; OLIVEIRA, Daniel Sabino de; CLAUDINO, Rinaldo; GONÇALVES, Marcos Vinicius Magno; DOURADO JUNIOR, Mario Emilio Teixeira. Intermediate-length CAG repeat in ATXN2 is associated with increased risk for amyotrophic lateral sclerosis in Brazilian patients. Neurobiology Of Aging, [S.L.], v. 69, p. 29215-29218, set. 2018. Elsevier BV. http://dx.doi.org/10.1016/j.neurobiolaging.2018.04.020. Disponível em: https://www.sciencedirect.com/science/article/pii/S0197458018301544?via%3Dihub. Acesso em: 19 jul. 2023.
dc.identifierhttps://repositorio.ufrn.br/handle/123456789/54237
dc.identifierhttps://doi.org/10.1016/j.neurobiolaging.2018.04.020
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/8604033
dc.descriptionIntermediate-length cytosine-adenine-guanine nucleotide repeat expansions in the ATXN2 gene (which encodes for the protein Ataxin-2) have been linked to increased risk for amyotrophic lateral sclerosis (ALS) in different populations. There is no such study in the Brazilian population, which has a mixed ethnic background. We have thus selected 459 patients with ALS (372 Sporadic ALS and 87 Familial ALS) and 468 control subjects from 6 Brazilian centers to investigate this point. We performed polymerase chain reaction to determine the length of the ATXN2 alleles. Polymerase chain reaction products were resolved using capillary electrophoresis on ABI 3500 × l capillary sequencer. We found that ATXN2 intermediate-length expansions (larger than 26 repeats) were associated with an increased risk for ALS (odds ratio = 2.56, 95% confidence interval: 1.29–5.08, p = 0.005). Phenotype in patients with and without ATXN2 expansions was similar. Our findings support the hypothesis that ATXN2 plays an important role in the pathogenesis of ALS also in the Brazilian population.
dc.languageen
dc.publisherElsevier
dc.subjectALS
dc.subjectATXN2 gene
dc.subjectbrazilian patients
dc.subjectrisk factor
dc.titleIntermediate-length CAG repeat in ATXN2 is associated with increased risk for amyotrophic lateral sclerosis in Brazilian patients
dc.typearticle


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