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Association of the Brain-derived Neurotrophic Factor Gene and Clinical Features of Bipolar Disorder in Korea
OBJECTIVE: Brain-derived neurotrophic factor (BDNF) plays an important role in cell survival, differentiation, and cell death as well as in neural plasticity. Recent studies have suggested that BDNF is involved in the pathogenesis of bipolar disorder. The aim of this study was to investigate the ass...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean College of Neuropsychopharmacology
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569161/ https://www.ncbi.nlm.nih.gov/pubmed/23430274 http://dx.doi.org/10.9758/cpn.2012.10.3.163 |
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author | Min, Hye Ji Cho, Hyun-Sang Kim, Se Joo Seok, Jeong-Ho Lee, Eun Jon, Duk-In |
author_facet | Min, Hye Ji Cho, Hyun-Sang Kim, Se Joo Seok, Jeong-Ho Lee, Eun Jon, Duk-In |
author_sort | Min, Hye Ji |
collection | PubMed |
description | OBJECTIVE: Brain-derived neurotrophic factor (BDNF) plays an important role in cell survival, differentiation, and cell death as well as in neural plasticity. Recent studies have suggested that BDNF is involved in the pathogenesis of bipolar disorder. The aim of this study was to investigate the association of the genetic variations of the BDNF gene with bipolar disorder in Korea. We also studied the possible association of these genetic variants with clinical features. METHODS: The allelic and genotypic distributions of Val66Met polymorphism of the BDNF gene were analyzed using a polymerase chain reaction-based method in 184 bipolar patients and 214 controls. Analysis was performed to investigate an association of the Val66Met polymorphism of the BDNF gene and the clinical features in bipolar patients. RESULTS: No significant difference was found between bipolar patients and controls in the genotype and allele frequencies for the investigated BDNF polymorphism. However, the age of onset of bipolar disorder among the Val/Val (25.57), Val/Met (30.42) and Met/Met (32.45) genotype groups were significantly different (p=0.037). CONCLUSION: This study suggests that Val66Met polymorphisms are unlikely to contribution to the genetic predisposition to bipolar disorder as a whole. But Val66Met polymorphism may be associated with age of onset of the disorder, further studies designed to investigate the relationship in a larger population may be warranted. |
format | Online Article Text |
id | pubmed-3569161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Korean College of Neuropsychopharmacology |
record_format | MEDLINE/PubMed |
spelling | pubmed-35691612013-02-21 Association of the Brain-derived Neurotrophic Factor Gene and Clinical Features of Bipolar Disorder in Korea Min, Hye Ji Cho, Hyun-Sang Kim, Se Joo Seok, Jeong-Ho Lee, Eun Jon, Duk-In Clin Psychopharmacol Neurosci Original Article OBJECTIVE: Brain-derived neurotrophic factor (BDNF) plays an important role in cell survival, differentiation, and cell death as well as in neural plasticity. Recent studies have suggested that BDNF is involved in the pathogenesis of bipolar disorder. The aim of this study was to investigate the association of the genetic variations of the BDNF gene with bipolar disorder in Korea. We also studied the possible association of these genetic variants with clinical features. METHODS: The allelic and genotypic distributions of Val66Met polymorphism of the BDNF gene were analyzed using a polymerase chain reaction-based method in 184 bipolar patients and 214 controls. Analysis was performed to investigate an association of the Val66Met polymorphism of the BDNF gene and the clinical features in bipolar patients. RESULTS: No significant difference was found between bipolar patients and controls in the genotype and allele frequencies for the investigated BDNF polymorphism. However, the age of onset of bipolar disorder among the Val/Val (25.57), Val/Met (30.42) and Met/Met (32.45) genotype groups were significantly different (p=0.037). CONCLUSION: This study suggests that Val66Met polymorphisms are unlikely to contribution to the genetic predisposition to bipolar disorder as a whole. But Val66Met polymorphism may be associated with age of onset of the disorder, further studies designed to investigate the relationship in a larger population may be warranted. Korean College of Neuropsychopharmacology 2012-12 2012-12-20 /pmc/articles/PMC3569161/ /pubmed/23430274 http://dx.doi.org/10.9758/cpn.2012.10.3.163 Text en Copyright© 2012, Korean College of Neuropsychopharmacology 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 Min, Hye Ji Cho, Hyun-Sang Kim, Se Joo Seok, Jeong-Ho Lee, Eun Jon, Duk-In Association of the Brain-derived Neurotrophic Factor Gene and Clinical Features of Bipolar Disorder in Korea |
title | Association of the Brain-derived Neurotrophic Factor Gene and Clinical Features of Bipolar Disorder in Korea |
title_full | Association of the Brain-derived Neurotrophic Factor Gene and Clinical Features of Bipolar Disorder in Korea |
title_fullStr | Association of the Brain-derived Neurotrophic Factor Gene and Clinical Features of Bipolar Disorder in Korea |
title_full_unstemmed | Association of the Brain-derived Neurotrophic Factor Gene and Clinical Features of Bipolar Disorder in Korea |
title_short | Association of the Brain-derived Neurotrophic Factor Gene and Clinical Features of Bipolar Disorder in Korea |
title_sort | association of the brain-derived neurotrophic factor gene and clinical features of bipolar disorder in korea |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569161/ https://www.ncbi.nlm.nih.gov/pubmed/23430274 http://dx.doi.org/10.9758/cpn.2012.10.3.163 |
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