Literature DB >> 22159055

The APOE ε2 allele increases the risk of earlier age at onset in Machado-Joseph disease.

Conceição Bettencourt1, Mafalda Raposo, Nadiya Kazachkova, Teresa Cymbron, Cristina Santos, Teresa Kay, João Vasconcelos, Patrícia Maciel, Karina C Donis, Maria Luiza Saraiva-Pereira, Laura B Jardim, Jorge Sequeiros, Manuela Lima.   

Abstract

OBJECTIVE: To investigate a modulating effect of the apolipoprotein E (APOE) polymorphism on age at onset of Machado-Joseph disease (MJD).
DESIGN: We collected blood samples from 192 patients with MJD and typed the APOE polymorphism. Patients The 192 patients with MJD included 59 from the Azores, 73 from mainland Portugal, and 60 from Brazil.
SETTING: Academic research center.
RESULTS: Cases with the ε2/ε3 genotype had an earlier onset compared with those with the ε3/ε3 or the ε3/ε4 genotype. In this series of patients, the presence of an APOE ε2 allele implies a decrease of nearly 5 years in the age at onset. When combining several other predictors in a general linear model, namely, the presence/absence of the APOE ε2 allele, with the size of the (CAG)(n) in expanded alleles, the model was significantly improved and the explanation of onset variance was raised from 59.8% to 66.5%. Furthermore, the presence of the ε2 allele was associated with an onset before age 39 years (odds ratio, 5.00; 95% CI, 1.18-21.14).
CONCLUSION: The polymorphism at the APOE gene plays a role as a genetic modifier of MJD phenotype.

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Year:  2011        PMID: 22159055     DOI: 10.1001/archneurol.2011.636

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  17 in total

1.  Sequence analysis of 5' regulatory regions of the Machado-Joseph disease gene (ATXN3).

Authors:  Conceição Bettencourt; Mafalda Raposo; Nadiya Kazachkova; Cristina Santos; Teresa Kay; João Vasconcelos; Patrícia Maciel; Karina C Donis; Maria Luiza Saraiva-Pereira; Laura B Jardim; Jorge Sequeiros; Jácome Bruges-Armas; Manuela Lima
Journal:  Cerebellum       Date:  2012-12       Impact factor: 3.847

2.  Promoter Variation and Expression Levels of Inflammatory Genes IL1A, IL1B, IL6 and TNF in Blood of Spinocerebellar Ataxia Type 3 (SCA3) Patients.

Authors:  Mafalda Raposo; Conceição Bettencourt; Amanda Ramos; Nadiya Kazachkova; João Vasconcelos; Teresa Kay; Jácome Bruges-Armas; Manuela Lima
Journal:  Neuromolecular Med       Date:  2016-05-31       Impact factor: 3.843

3.  Transcript diversity of Machado-Joseph disease gene (ATXN3) is not directly determined by SNPs in exonic or flanking intronic regions.

Authors:  Conceição Bettencourt; Mafalda Raposo; Raquel Ros; Rafael Montiel; Jácome Bruges-Armas; Manuela Lima
Journal:  J Mol Neurosci       Date:  2012-06-16       Impact factor: 3.444

4.  High Serum GFAP Levels in SCA3/MJD May Not Correlate with Disease Progression.

Authors:  Yuting Shi; Chunrong Wang; Fengzhen Huang; Zhao Chen; Zhanfang Sun; Junling Wang; Beisha Tang; Tetsuo Ashizawa; Thomas Klockgether; Hong Jiang
Journal:  Cerebellum       Date:  2015-12       Impact factor: 3.847

5.  Genetic Variation in ATXN3 (Ataxin-3) 3'UTR: Insights into the Downstream Regulatory Elements of the Causative Gene of Machado-Joseph Disease/Spinocerebellar Ataxia Type 3.

Authors:  Ana Rosa Vieira Melo; Mafalda Raposo; Marta Ventura; Sandra Martins; Sara Pavão; Isabel Alonso; Conceição Bettencourt; Manuela Lima
Journal:  Cerebellum       Date:  2022-01-16       Impact factor: 3.847

6.  Variants in RBP4 and AR genes modulate age at onset in familial amyloid polyneuropathy (FAP ATTRV30M).

Authors:  Diana Santos; Teresa Coelho; Miguel Alves-Ferreira; Jorge Sequeiros; Denisa Mendonça; Isabel Alonso; Carolina Lemos; Alda Sousa
Journal:  Eur J Hum Genet       Date:  2015-08-19       Impact factor: 4.246

7.  Spinocerebellar ataxia type 3 in Israel: phenotype and genotype of a Jew Yemenite subpopulation.

Authors:  Roy Zaltzman; Reuven Sharony; Colin Klein; Carlos R Gordon
Journal:  J Neurol       Date:  2016-08-08       Impact factor: 4.849

8.  Spinocerebellar ataxias in Brazil--frequencies and modulating effects of related genes.

Authors:  Raphael Machado de Castilhos; Gabriel Vasata Furtado; Tailise Conte Gheno; Paola Schaeffer; Aline Russo; Orlando Barsottini; José Luiz Pedroso; Diego Z Salarini; Fernando Regla Vargas; Maria Angélica de Faria Domingues de Lima; Clécio Godeiro; Luiz Carlos Santana-da-Silva; Maria Betânia Pereira Toralles; Silvana Santos; Hélio van der Linden; Hector Yuri Wanderley; Paula Frassineti Vanconcelos de Medeiros; Eliana Ternes Pereira; Erlane Ribeiro; Maria Luiza Saraiva-Pereira; Laura Bannach Jardim
Journal:  Cerebellum       Date:  2014-02       Impact factor: 3.847

9.  Analysis of the GGGGCC Repeat Expansions of the C9orf72 Gene in SCA3/MJD Patients from China.

Authors:  Chunrong Wang; Zhao Chen; Fang Yang; Bin Jiao; Huirong Peng; Yuting Shi; Yaqin Wang; Fengzhen Huang; Junling Wang; Lu Shen; Kun Xia; Beisha Tang; Tetsuo Ashizawa; Hong Jiang
Journal:  PLoS One       Date:  2015-06-17       Impact factor: 3.240

10.  Two novel SNPs in ATXN3 3' UTR may decrease age at onset of SCA3/MJD in Chinese patients.

Authors:  Zhe Long; Zhao Chen; Chunrong Wang; Fengzhen Huang; Huirong Peng; Xuan Hou; Dongxue Ding; Wei Ye; Junling Wang; Qian Pan; Jiada Li; Kun Xia; Beisha Tang; Tetsuo Ashizawa; Hong Jiang
Journal:  PLoS One       Date:  2015-02-17       Impact factor: 3.240

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