Catechol-O-Methyltransferase Genetic Variant Associated with the Risk of Alzheimer's Disease in a Brazilian Population

被引:7
|
作者
Pereira, Patricia Araujo [1 ]
Romano-Silva, Marco Aurelio [1 ]
Camargos Bicalho, Maria Aparecida [2 ]
de Moraes, Edgar Nunes [1 ,2 ]
Malloy-Diniz, Leandro [1 ,2 ]
Garcia Santos Pimenta, Guilherme Jose [1 ]
Mello, Marina Pena [1 ]
Reis Sguizzato Bozzi, Isadora Cristine [1 ]
de Marco, Luiz Armando [1 ]
Nicolato, Rodrigo [1 ]
Miranda, Debora Marques [1 ]
机构
[1] Univ Fed Minas Gerais, Fac Med, INCT Med Mol, BR-30130100 Belo Horizonte, MG, Brazil
[2] Univ Fed Minas Gerais, Hosp Clin, Ctr Jenny Faria Assistencia Saude Idoso & Mulher, BR-30130100 Belo Horizonte, MG, Brazil
关键词
Catechol-O-methyltransferase; Single-nucleotide polymorphism; Alzheimer's disease; Behavioral and psychological symptoms of dementia; POLYMORPHISM; PSYCHOSIS; COMT; DEMENTIA; SYMPTOMS; SCHIZOPHRENIA; AGGRESSION; PREDICTORS; HAPLOTYPES; PHENOTYPE;
D O I
10.1159/000341578
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The aim of the present study was to examine the association between polymorphism in the catechol-O-methyltransferase (COMT) gene and Alzheimer's disease (AD) in a Brazilian population. The case-control method was used to study the association between AD and genetic variants of COMT. Six tag single-nucleotide polymorphisms (SNPs) in the COMT gene were genotyped by RT-PCR. Our findings showed that the 6 tag SNPs analyzed in this study were not associated with AD at the allele and genotype levels in comparison with the control group. No statistical difference was found between groups with and without behavioral and psychological symptoms of dementia (BPSD). Our results do not support the hypothesis that the polymorphisms of the COMT gene may be associated with susceptibility to AD with and without BPSD. Copyright (C) 2012 S. Karger AG, Basel
引用
收藏
页码:90 / 95
页数:6
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