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Association between the BDNF Val66Met Polymorphism and Chronicity of Depression
Article em En | WPRIM | ID: wpr-17597
Biblioteca responsável: WPRO
ABSTRACT
OBJECTIVE: Both clinical and biological factors influence the course of depressive disorders. This study tested for associations between the brain-derived neurotrophic factor (BDNF) gene at the Val66Met locus and the course of major depressive disorder (MDD). METHODS: Three hundred ten Korean subjects (209 patients, 101 controls) were genotyped for rs6265 at nucleotide 196 (G/A), which produces an amino acid substitution at codon 66 (Val66Met) of the gene for BDNF. Course of illness was evaluated both by chronicity of current episode (episode duration >24 months) and by the lifetime history of recurrences. RESULTS: Patients with the Met/Met BDNF genotype had a significantly higher rate of chronic depression than all others. There was a significant dose effect of the Met allele on chronicity. Compared with the Val/Val genotype, the relative risk of chronicity was 1.67 for the Val/Met genotype, and 2.58 for the Met/Met genotype. Lifetime history of recurrent episodes was not related to BDNF genotypes but was significantly associated with younger age of onset and with a history of depression in first degree relatives. CONCLUSION: BDNF genotyping may be informative for anticipating chronicity in major depression.
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Texto completo: 1 Base de dados: WPRIM Assunto principal: Códon / Fatores Biológicos / Idade de Início / Fator Neurotrófico Derivado do Encéfalo / Substituição de Aminoácidos / Depressão / Transtorno Depressivo Maior / Transtorno Depressivo / Alelos / Genótipo Tipo de estudo: Etiology_studies Limite: Humans Idioma: En Revista: Psychiatry Investigation Ano de publicação: 2013 Tipo de documento: Article
Texto completo: 1 Base de dados: WPRIM Assunto principal: Códon / Fatores Biológicos / Idade de Início / Fator Neurotrófico Derivado do Encéfalo / Substituição de Aminoácidos / Depressão / Transtorno Depressivo Maior / Transtorno Depressivo / Alelos / Genótipo Tipo de estudo: Etiology_studies Limite: Humans Idioma: En Revista: Psychiatry Investigation Ano de publicação: 2013 Tipo de documento: Article