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Association of BDNF Val66Met Polymorphism and Brain BDNF Levels with Major Depression and Suicide

BACKGROUND: Brain-derived neurotrophic factor is implicated in the pathophysiology of major depressive disorder and suicide. Both are partly caused by early life adversity, which reduces brain-derived neurotrophic factor protein levels. This study examines the association of brain-derived neurotroph...

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Autores principales: Youssef, Mariam M, Underwood, Mark D, Huang, Yung-Yu, Hsiung, Shu-chi, Liu, Yan, Simpson, Norman R, Bakalian, Mihran J, Rosoklija, Gorazd B, Dwork, Andrew J, Arango, Victoria, Mann, J John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6007393/
https://www.ncbi.nlm.nih.gov/pubmed/29432620
http://dx.doi.org/10.1093/ijnp/pyy008
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author Youssef, Mariam M
Underwood, Mark D
Huang, Yung-Yu
Hsiung, Shu-chi
Liu, Yan
Simpson, Norman R
Bakalian, Mihran J
Rosoklija, Gorazd B
Dwork, Andrew J
Arango, Victoria
Mann, J John
author_facet Youssef, Mariam M
Underwood, Mark D
Huang, Yung-Yu
Hsiung, Shu-chi
Liu, Yan
Simpson, Norman R
Bakalian, Mihran J
Rosoklija, Gorazd B
Dwork, Andrew J
Arango, Victoria
Mann, J John
author_sort Youssef, Mariam M
collection PubMed
description BACKGROUND: Brain-derived neurotrophic factor is implicated in the pathophysiology of major depressive disorder and suicide. Both are partly caused by early life adversity, which reduces brain-derived neurotrophic factor protein levels. This study examines the association of brain-derived neurotrophic factor Val66Met polymorphism and brain brain-derived neurotrophic factor levels with depression and suicide. We hypothesized that both major depressive disorder and early life adversity would be associated with the Met allele and lower brain brain-derived neurotrophic factor levels. Such an association would be consistent with low brain-derived neurotrophic factor mediating the effect of early life adversity on adulthood suicide and major depressive disorder. METHODS: Brain-derived neurotrophic factor Val66Met polymorphism was genotyped in postmortem brains of 37 suicide decedents and 53 nonsuicides. Additionally, brain-derived neurotrophic factor protein levels were determined by Western blot in dorsolateral prefrontal cortex (Brodmann area 9), anterior cingulate cortex (Brodmann area 24), caudal brainstem, and rostral brainstem. The relationships between these measures and major depressive disorder, death by suicide, and reported early life adversity were examined. RESULTS: Subjects with the Met allele had an increased risk for depression. Depressed patients also have lower brain-derived neurotrophic factor levels in anterior cingulate cortex and caudal brainstem compared with nondepressed subjects. No effect of history of suicide death or early life adversity was observed with genotype, but lower brain-derived neurotrophic factor levels in the anterior cingulate cortex were found in subjects who had been exposed to early life adversity and/or died by suicide compared with nonsuicide decedents and no reported early life adversity. CONCLUSIONS: This study provides further evidence implicating low brain brain-derived neurotrophic factor and the brain-derived neurotrophic factor Met allele in major depression risk. Future studies should seek to determine how altered brain-derived neurotrophic factor expression contributes to depression and suicide.
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spelling pubmed-60073932019-02-08 Association of BDNF Val66Met Polymorphism and Brain BDNF Levels with Major Depression and Suicide Youssef, Mariam M Underwood, Mark D Huang, Yung-Yu Hsiung, Shu-chi Liu, Yan Simpson, Norman R Bakalian, Mihran J Rosoklija, Gorazd B Dwork, Andrew J Arango, Victoria Mann, J John Int J Neuropsychopharmacol Regular Research Articles BACKGROUND: Brain-derived neurotrophic factor is implicated in the pathophysiology of major depressive disorder and suicide. Both are partly caused by early life adversity, which reduces brain-derived neurotrophic factor protein levels. This study examines the association of brain-derived neurotrophic factor Val66Met polymorphism and brain brain-derived neurotrophic factor levels with depression and suicide. We hypothesized that both major depressive disorder and early life adversity would be associated with the Met allele and lower brain brain-derived neurotrophic factor levels. Such an association would be consistent with low brain-derived neurotrophic factor mediating the effect of early life adversity on adulthood suicide and major depressive disorder. METHODS: Brain-derived neurotrophic factor Val66Met polymorphism was genotyped in postmortem brains of 37 suicide decedents and 53 nonsuicides. Additionally, brain-derived neurotrophic factor protein levels were determined by Western blot in dorsolateral prefrontal cortex (Brodmann area 9), anterior cingulate cortex (Brodmann area 24), caudal brainstem, and rostral brainstem. The relationships between these measures and major depressive disorder, death by suicide, and reported early life adversity were examined. RESULTS: Subjects with the Met allele had an increased risk for depression. Depressed patients also have lower brain-derived neurotrophic factor levels in anterior cingulate cortex and caudal brainstem compared with nondepressed subjects. No effect of history of suicide death or early life adversity was observed with genotype, but lower brain-derived neurotrophic factor levels in the anterior cingulate cortex were found in subjects who had been exposed to early life adversity and/or died by suicide compared with nonsuicide decedents and no reported early life adversity. CONCLUSIONS: This study provides further evidence implicating low brain brain-derived neurotrophic factor and the brain-derived neurotrophic factor Met allele in major depression risk. Future studies should seek to determine how altered brain-derived neurotrophic factor expression contributes to depression and suicide. Oxford University Press 2018-02-08 /pmc/articles/PMC6007393/ /pubmed/29432620 http://dx.doi.org/10.1093/ijnp/pyy008 Text en Published by Oxford University Press on behalf of CINP 2018. This work is written by (a) US Government employee(s) and is in the public domain in the US. http://www.nationalarchives.gov.uk/doc/open-government-licence/version/2/ This Open Access article contains public sector information licensed under the Open Government Licence v2.0 (http://www.nationalarchives.gov.uk/doc/open-government-licence/version/2/).
spellingShingle Regular Research Articles
Youssef, Mariam M
Underwood, Mark D
Huang, Yung-Yu
Hsiung, Shu-chi
Liu, Yan
Simpson, Norman R
Bakalian, Mihran J
Rosoklija, Gorazd B
Dwork, Andrew J
Arango, Victoria
Mann, J John
Association of BDNF Val66Met Polymorphism and Brain BDNF Levels with Major Depression and Suicide
title Association of BDNF Val66Met Polymorphism and Brain BDNF Levels with Major Depression and Suicide
title_full Association of BDNF Val66Met Polymorphism and Brain BDNF Levels with Major Depression and Suicide
title_fullStr Association of BDNF Val66Met Polymorphism and Brain BDNF Levels with Major Depression and Suicide
title_full_unstemmed Association of BDNF Val66Met Polymorphism and Brain BDNF Levels with Major Depression and Suicide
title_short Association of BDNF Val66Met Polymorphism and Brain BDNF Levels with Major Depression and Suicide
title_sort association of bdnf val66met polymorphism and brain bdnf levels with major depression and suicide
topic Regular Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6007393/
https://www.ncbi.nlm.nih.gov/pubmed/29432620
http://dx.doi.org/10.1093/ijnp/pyy008
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