Cargando…

Genotype-dependent associations between serotonin transporter gene (SLC6A4) DNA methylation and late-life depression

BACKGROUND: Disrupted serotonergic signaling is often a feature of depression and the role of the serotonin transporter gene (SLC6A4), responsible for serotonin re-uptake, has received much attention in this regard. Most studies have focused on the polymorphic 5-HTTLPR upstream repeat, or DNA methyl...

Descripción completa

Detalles Bibliográficos
Autores principales: Lam, Dilys, Ancelin, Marie-Laure, Ritchie, Karen, Freak-Poli, Rosanne, Saffery, Richard, Ryan, Joanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6122720/
https://www.ncbi.nlm.nih.gov/pubmed/30180828
http://dx.doi.org/10.1186/s12888-018-1850-4
_version_ 1783352711101546496
author Lam, Dilys
Ancelin, Marie-Laure
Ritchie, Karen
Freak-Poli, Rosanne
Saffery, Richard
Ryan, Joanne
author_facet Lam, Dilys
Ancelin, Marie-Laure
Ritchie, Karen
Freak-Poli, Rosanne
Saffery, Richard
Ryan, Joanne
author_sort Lam, Dilys
collection PubMed
description BACKGROUND: Disrupted serotonergic signaling is often a feature of depression and the role of the serotonin transporter gene (SLC6A4), responsible for serotonin re-uptake, has received much attention in this regard. Most studies have focused on the polymorphic 5-HTTLPR upstream repeat, or DNA methylation at the promoter CpG island. Few studies have explored the influence of genetic variation across the gene on DNA methylation, and their combined association with depression risk. The aim of this study was to determine whether genetic variation in the SLC6A4 gene influences promoter DNA methylation, and whether these are associated with depression status. METHOD: The ESPRIT study involves a community-based population of older individuals (> 65 years of age). Major depressive disorder (MDD) was diagnosed according to DSM-IV (American Psychiatric Association, 1994) criteria, and severe depressive symptoms assessed by the Centre for Epidemiological Studies Depression (CES-D) Scale. Sequenom MassARRAY was used to measure SLC6A4 methylation status (n = 302). RESULTS: Nominally significant associations were observed between SLC6A4 genetic variants (5-HTTLPR, rs140700, rs4251417, rs6354, rs25528, rs25531) and DNA methylation at several CpG sites. In multivariate regression, DNA methylation was associated with depression status, but only in the presence of specific genotypes. In individuals homozygous for the short 5-HTTLPR and 5-HTTLPR/r25531 alleles, lower methylation at two CpGs was associated with depression (β = − 0.44 to β = − 0.31; p = 0.001 to p = 0.038). CONCLUSION: We present evidence for genotype-dependent associations between SLC6A4 methylation and depression. Genetic variants may also play a role in influencing promoter methylation levels and its association with depression. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12888-018-1850-4) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6122720
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-61227202018-09-10 Genotype-dependent associations between serotonin transporter gene (SLC6A4) DNA methylation and late-life depression Lam, Dilys Ancelin, Marie-Laure Ritchie, Karen Freak-Poli, Rosanne Saffery, Richard Ryan, Joanne BMC Psychiatry Research Article BACKGROUND: Disrupted serotonergic signaling is often a feature of depression and the role of the serotonin transporter gene (SLC6A4), responsible for serotonin re-uptake, has received much attention in this regard. Most studies have focused on the polymorphic 5-HTTLPR upstream repeat, or DNA methylation at the promoter CpG island. Few studies have explored the influence of genetic variation across the gene on DNA methylation, and their combined association with depression risk. The aim of this study was to determine whether genetic variation in the SLC6A4 gene influences promoter DNA methylation, and whether these are associated with depression status. METHOD: The ESPRIT study involves a community-based population of older individuals (> 65 years of age). Major depressive disorder (MDD) was diagnosed according to DSM-IV (American Psychiatric Association, 1994) criteria, and severe depressive symptoms assessed by the Centre for Epidemiological Studies Depression (CES-D) Scale. Sequenom MassARRAY was used to measure SLC6A4 methylation status (n = 302). RESULTS: Nominally significant associations were observed between SLC6A4 genetic variants (5-HTTLPR, rs140700, rs4251417, rs6354, rs25528, rs25531) and DNA methylation at several CpG sites. In multivariate regression, DNA methylation was associated with depression status, but only in the presence of specific genotypes. In individuals homozygous for the short 5-HTTLPR and 5-HTTLPR/r25531 alleles, lower methylation at two CpGs was associated with depression (β = − 0.44 to β = − 0.31; p = 0.001 to p = 0.038). CONCLUSION: We present evidence for genotype-dependent associations between SLC6A4 methylation and depression. Genetic variants may also play a role in influencing promoter methylation levels and its association with depression. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12888-018-1850-4) contains supplementary material, which is available to authorized users. BioMed Central 2018-09-04 /pmc/articles/PMC6122720/ /pubmed/30180828 http://dx.doi.org/10.1186/s12888-018-1850-4 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Lam, Dilys
Ancelin, Marie-Laure
Ritchie, Karen
Freak-Poli, Rosanne
Saffery, Richard
Ryan, Joanne
Genotype-dependent associations between serotonin transporter gene (SLC6A4) DNA methylation and late-life depression
title Genotype-dependent associations between serotonin transporter gene (SLC6A4) DNA methylation and late-life depression
title_full Genotype-dependent associations between serotonin transporter gene (SLC6A4) DNA methylation and late-life depression
title_fullStr Genotype-dependent associations between serotonin transporter gene (SLC6A4) DNA methylation and late-life depression
title_full_unstemmed Genotype-dependent associations between serotonin transporter gene (SLC6A4) DNA methylation and late-life depression
title_short Genotype-dependent associations between serotonin transporter gene (SLC6A4) DNA methylation and late-life depression
title_sort genotype-dependent associations between serotonin transporter gene (slc6a4) dna methylation and late-life depression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6122720/
https://www.ncbi.nlm.nih.gov/pubmed/30180828
http://dx.doi.org/10.1186/s12888-018-1850-4
work_keys_str_mv AT lamdilys genotypedependentassociationsbetweenserotonintransportergeneslc6a4dnamethylationandlatelifedepression
AT ancelinmarielaure genotypedependentassociationsbetweenserotonintransportergeneslc6a4dnamethylationandlatelifedepression
AT ritchiekaren genotypedependentassociationsbetweenserotonintransportergeneslc6a4dnamethylationandlatelifedepression
AT freakpolirosanne genotypedependentassociationsbetweenserotonintransportergeneslc6a4dnamethylationandlatelifedepression
AT safferyrichard genotypedependentassociationsbetweenserotonintransportergeneslc6a4dnamethylationandlatelifedepression
AT ryanjoanne genotypedependentassociationsbetweenserotonintransportergeneslc6a4dnamethylationandlatelifedepression