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Association between the BDNF Val66Met Polymorphism and Chronicity of Depression

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 subjec...

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Autores principales: Lee, Yujin, Lim, Shinn Won, Kim, Soo Yeon, Chung, Jae Won, Kim, Jinwoo, Myung, Woojae, Song, Jihae, Kim, Seonwoo, Carroll, Bernard J, Kim, Doh Kwan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Neuropsychiatric Association 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3590431/
https://www.ncbi.nlm.nih.gov/pubmed/23482723
http://dx.doi.org/10.4306/pi.2013.10.1.56
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author Lee, Yujin
Lim, Shinn Won
Kim, Soo Yeon
Chung, Jae Won
Kim, Jinwoo
Myung, Woojae
Song, Jihae
Kim, Seonwoo
Carroll, Bernard J
Kim, Doh Kwan
author_facet Lee, Yujin
Lim, Shinn Won
Kim, Soo Yeon
Chung, Jae Won
Kim, Jinwoo
Myung, Woojae
Song, Jihae
Kim, Seonwoo
Carroll, Bernard J
Kim, Doh Kwan
author_sort Lee, Yujin
collection PubMed
description 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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spelling pubmed-35904312013-03-12 Association between the BDNF Val66Met Polymorphism and Chronicity of Depression Lee, Yujin Lim, Shinn Won Kim, Soo Yeon Chung, Jae Won Kim, Jinwoo Myung, Woojae Song, Jihae Kim, Seonwoo Carroll, Bernard J Kim, Doh Kwan Psychiatry Investig Original Article 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. Korean Neuropsychiatric Association 2013-03 2013-01-24 /pmc/articles/PMC3590431/ /pubmed/23482723 http://dx.doi.org/10.4306/pi.2013.10.1.56 Text en Copyright © 2013 Korean Neuropsychiatric Association http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Yujin
Lim, Shinn Won
Kim, Soo Yeon
Chung, Jae Won
Kim, Jinwoo
Myung, Woojae
Song, Jihae
Kim, Seonwoo
Carroll, Bernard J
Kim, Doh Kwan
Association between the BDNF Val66Met Polymorphism and Chronicity of Depression
title Association between the BDNF Val66Met Polymorphism and Chronicity of Depression
title_full Association between the BDNF Val66Met Polymorphism and Chronicity of Depression
title_fullStr Association between the BDNF Val66Met Polymorphism and Chronicity of Depression
title_full_unstemmed Association between the BDNF Val66Met Polymorphism and Chronicity of Depression
title_short Association between the BDNF Val66Met Polymorphism and Chronicity of Depression
title_sort association between the bdnf val66met polymorphism and chronicity of depression
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3590431/
https://www.ncbi.nlm.nih.gov/pubmed/23482723
http://dx.doi.org/10.4306/pi.2013.10.1.56
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