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A Longitudinal Study of BDNF Promoter Methylation and Depression in Breast Cancer
OBJECTIVE: Brain-derived neurotrophic factor (BDNF) is investigated in depression related to medical disorders and its secretion is influenced by epigenetic factors. We investigated the association between BDNF promoter methylation and depression following mastectomy for breast cancer. METHODS: In t...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Korean Neuropsychiatric Association
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620310/ https://www.ncbi.nlm.nih.gov/pubmed/26508964 http://dx.doi.org/10.4306/pi.2015.12.4.523 |
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author | Kang, Hee-Ju Kim, Jae-Min Kim, Seon-Young Kim, Sung-Wan Shin, Il-Seon Kim, Hye-Ran Park, Min-Ho Shin, Myung-Geun Yoon, Jung-Han Yoon, Jin-Sang |
author_facet | Kang, Hee-Ju Kim, Jae-Min Kim, Seon-Young Kim, Sung-Wan Shin, Il-Seon Kim, Hye-Ran Park, Min-Ho Shin, Myung-Geun Yoon, Jung-Han Yoon, Jin-Sang |
author_sort | Kang, Hee-Ju |
collection | PubMed |
description | OBJECTIVE: Brain-derived neurotrophic factor (BDNF) is investigated in depression related to medical disorders and its secretion is influenced by epigenetic factors. We investigated the association between BDNF promoter methylation and depression following mastectomy for breast cancer. METHODS: In total, 309 patients with breast cancer were evaluated 1 week after mastectomy, and 244 (79%) were followed up 1 year later. Depression was diagnosed (major or minor depressive disorder) according to DSM-IV criteria and depression severity was estimated by Montgomery-Asberg Depression Rating Scale (MADRS). We assessed BDNF promoter methylation using leukocyte DNA. The effects of BDNF methylation on depression diagnosis and severity were investigated using multivariate logistic and linear regression models, respectively. The two-way interaction between BDNF methylation and the val66met polymorphism on depression was also evaluated using multivariate logistic regression models. RESULTS: Higher BDNF methylation was independently associated with depression diagnosis and with more severe symptoms at both 1 week and 1 year after mastectomy. No significant methylation-genotype interactions were found. CONCLUSION: A role for BDNF in depression related to breast cancer was supported. Indeed, the association between depression and BDNF methylation may be useful for identifying patients who are at high risk for depression and for suggesting directions for promising drug research. |
format | Online Article Text |
id | pubmed-4620310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Korean Neuropsychiatric Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-46203102015-10-27 A Longitudinal Study of BDNF Promoter Methylation and Depression in Breast Cancer Kang, Hee-Ju Kim, Jae-Min Kim, Seon-Young Kim, Sung-Wan Shin, Il-Seon Kim, Hye-Ran Park, Min-Ho Shin, Myung-Geun Yoon, Jung-Han Yoon, Jin-Sang Psychiatry Investig Original Article OBJECTIVE: Brain-derived neurotrophic factor (BDNF) is investigated in depression related to medical disorders and its secretion is influenced by epigenetic factors. We investigated the association between BDNF promoter methylation and depression following mastectomy for breast cancer. METHODS: In total, 309 patients with breast cancer were evaluated 1 week after mastectomy, and 244 (79%) were followed up 1 year later. Depression was diagnosed (major or minor depressive disorder) according to DSM-IV criteria and depression severity was estimated by Montgomery-Asberg Depression Rating Scale (MADRS). We assessed BDNF promoter methylation using leukocyte DNA. The effects of BDNF methylation on depression diagnosis and severity were investigated using multivariate logistic and linear regression models, respectively. The two-way interaction between BDNF methylation and the val66met polymorphism on depression was also evaluated using multivariate logistic regression models. RESULTS: Higher BDNF methylation was independently associated with depression diagnosis and with more severe symptoms at both 1 week and 1 year after mastectomy. No significant methylation-genotype interactions were found. CONCLUSION: A role for BDNF in depression related to breast cancer was supported. Indeed, the association between depression and BDNF methylation may be useful for identifying patients who are at high risk for depression and for suggesting directions for promising drug research. Korean Neuropsychiatric Association 2015-10 2015-09-30 /pmc/articles/PMC4620310/ /pubmed/26508964 http://dx.doi.org/10.4306/pi.2015.12.4.523 Text en Copyright © 2015 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 Kang, Hee-Ju Kim, Jae-Min Kim, Seon-Young Kim, Sung-Wan Shin, Il-Seon Kim, Hye-Ran Park, Min-Ho Shin, Myung-Geun Yoon, Jung-Han Yoon, Jin-Sang A Longitudinal Study of BDNF Promoter Methylation and Depression in Breast Cancer |
title | A Longitudinal Study of BDNF Promoter Methylation and Depression in Breast Cancer |
title_full | A Longitudinal Study of BDNF Promoter Methylation and Depression in Breast Cancer |
title_fullStr | A Longitudinal Study of BDNF Promoter Methylation and Depression in Breast Cancer |
title_full_unstemmed | A Longitudinal Study of BDNF Promoter Methylation and Depression in Breast Cancer |
title_short | A Longitudinal Study of BDNF Promoter Methylation and Depression in Breast Cancer |
title_sort | longitudinal study of bdnf promoter methylation and depression in breast cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620310/ https://www.ncbi.nlm.nih.gov/pubmed/26508964 http://dx.doi.org/10.4306/pi.2015.12.4.523 |
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