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Genetic Role of BDNF Val66Met and 5-HTTLPR Polymorphisms on Depressive Disorder

OBJECTIVE: We investigated possible association between depressive disorders and BDNF Val66Met and 5-HTTLPR. Brain derived neurotrophic factor (BDNF) gene and serotonin transporter (SLC6A4) gene are promising candidate genes for depressive disorders. It has been suggested that BDNF promotes the surv...

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Autores principales: Lee, Kyu Young, Jeong, Seong Hoon, Kim, Se Hyun, Ahn, Yong Min, Kim, Yong Sik, Jung, Hee Yeon, Bang, Yang Weon, Joo, Eun-Jeong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Neuropsychiatric Association 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4023095/
https://www.ncbi.nlm.nih.gov/pubmed/24843376
http://dx.doi.org/10.4306/pi.2014.11.2.192
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author Lee, Kyu Young
Jeong, Seong Hoon
Kim, Se Hyun
Ahn, Yong Min
Kim, Yong Sik
Jung, Hee Yeon
Bang, Yang Weon
Joo, Eun-Jeong
author_facet Lee, Kyu Young
Jeong, Seong Hoon
Kim, Se Hyun
Ahn, Yong Min
Kim, Yong Sik
Jung, Hee Yeon
Bang, Yang Weon
Joo, Eun-Jeong
author_sort Lee, Kyu Young
collection PubMed
description OBJECTIVE: We investigated possible association between depressive disorders and BDNF Val66Met and 5-HTTLPR. Brain derived neurotrophic factor (BDNF) gene and serotonin transporter (SLC6A4) gene are promising candidate genes for depressive disorders. It has been suggested that BDNF promotes the survival and differentiation of serotonergic neurons and that serotonergic transmission exerts powerful control over BDNF gene expression. METHODS: Final analyses were performed on 186 patients with depressive disorders and 1032 controls. Val66Met polymorphism of BDNF gene and 5-HTTLPR polymorphism of serotonin transporter gene were genotyped and allele and genotypic associations on the diagnosis of depression and age at onset of depression were analyzed. RESULTS: The 5-HTTLPR was positively associated with depressive affected status in the total sample and in females (p=0.038 for allelewise, p=0.015 for genotype-wise associations), but, not in males. The BDNF Val66Met showed no association with depression. BDNF Val66Met and 5-HTTLPR alone were not associated with age at onset of depression. Additional analysis on the interaction between BDNF Val66Met and 5-HTTLPR found a significant association with age at onset of depression in the entire patient group. This association was also found in the female but not in the male patient group. None of the positive results survived Bonferroni correction for multiple testing. CONCLUSION: This result suggested that BDNF Val66Met and 5-HTTLPR may contribute to depressive disorders in a complex way and that the genetic effect could differ by gender. Further studies with large number of patients will be necessary.
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spelling pubmed-40230952014-05-19 Genetic Role of BDNF Val66Met and 5-HTTLPR Polymorphisms on Depressive Disorder Lee, Kyu Young Jeong, Seong Hoon Kim, Se Hyun Ahn, Yong Min Kim, Yong Sik Jung, Hee Yeon Bang, Yang Weon Joo, Eun-Jeong Psychiatry Investig Original Article OBJECTIVE: We investigated possible association between depressive disorders and BDNF Val66Met and 5-HTTLPR. Brain derived neurotrophic factor (BDNF) gene and serotonin transporter (SLC6A4) gene are promising candidate genes for depressive disorders. It has been suggested that BDNF promotes the survival and differentiation of serotonergic neurons and that serotonergic transmission exerts powerful control over BDNF gene expression. METHODS: Final analyses were performed on 186 patients with depressive disorders and 1032 controls. Val66Met polymorphism of BDNF gene and 5-HTTLPR polymorphism of serotonin transporter gene were genotyped and allele and genotypic associations on the diagnosis of depression and age at onset of depression were analyzed. RESULTS: The 5-HTTLPR was positively associated with depressive affected status in the total sample and in females (p=0.038 for allelewise, p=0.015 for genotype-wise associations), but, not in males. The BDNF Val66Met showed no association with depression. BDNF Val66Met and 5-HTTLPR alone were not associated with age at onset of depression. Additional analysis on the interaction between BDNF Val66Met and 5-HTTLPR found a significant association with age at onset of depression in the entire patient group. This association was also found in the female but not in the male patient group. None of the positive results survived Bonferroni correction for multiple testing. CONCLUSION: This result suggested that BDNF Val66Met and 5-HTTLPR may contribute to depressive disorders in a complex way and that the genetic effect could differ by gender. Further studies with large number of patients will be necessary. Korean Neuropsychiatric Association 2014-04 2014-04-11 /pmc/articles/PMC4023095/ /pubmed/24843376 http://dx.doi.org/10.4306/pi.2014.11.2.192 Text en Copyright © 2014 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, Kyu Young
Jeong, Seong Hoon
Kim, Se Hyun
Ahn, Yong Min
Kim, Yong Sik
Jung, Hee Yeon
Bang, Yang Weon
Joo, Eun-Jeong
Genetic Role of BDNF Val66Met and 5-HTTLPR Polymorphisms on Depressive Disorder
title Genetic Role of BDNF Val66Met and 5-HTTLPR Polymorphisms on Depressive Disorder
title_full Genetic Role of BDNF Val66Met and 5-HTTLPR Polymorphisms on Depressive Disorder
title_fullStr Genetic Role of BDNF Val66Met and 5-HTTLPR Polymorphisms on Depressive Disorder
title_full_unstemmed Genetic Role of BDNF Val66Met and 5-HTTLPR Polymorphisms on Depressive Disorder
title_short Genetic Role of BDNF Val66Met and 5-HTTLPR Polymorphisms on Depressive Disorder
title_sort genetic role of bdnf val66met and 5-httlpr polymorphisms on depressive disorder
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4023095/
https://www.ncbi.nlm.nih.gov/pubmed/24843376
http://dx.doi.org/10.4306/pi.2014.11.2.192
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