DNA methylation at the neonatal state and at the time of diagnosis. Preliminary support for an association with the estrogen receptor 1, gamma-aminobutyric acid B receptor 1, and myelin oligodendrocyte glycoprotein in female adolescent patients with OCD

Obsessive-compulsive disorder (OCD) is a neuropsychiatric disorder. Non-genetic factors and their interaction with genes have attracted increasing attention. Epigenetics is regarded an important interface between environmental signals and activation/repression of genomic responses. Epigenetic mechan...

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Main Authors: Judith Becker Nissen, Christine Søholm Hansen, Anna eStarnawska, Manuel eMattheisen, Anders Dupont Børglum, Henriette Nørmølle Buttenschøn, Mads eHollegaard
Format: Article
Language:English
Published: Frontiers Media S.A. 2016-03-01
Series:Frontiers in Psychiatry
Subjects:
OCD
Online Access:http://journal.frontiersin.org/Journal/10.3389/fpsyt.2016.00035/full
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spelling doaj-7b37ccc7f4324bbabc6b5b470c3e568b2020-11-24T23:48:55ZengFrontiers Media S.A.Frontiers in Psychiatry1664-06402016-03-01710.3389/fpsyt.2016.00035169166DNA methylation at the neonatal state and at the time of diagnosis. Preliminary support for an association with the estrogen receptor 1, gamma-aminobutyric acid B receptor 1, and myelin oligodendrocyte glycoprotein in female adolescent patients with OCDJudith Becker Nissen0Christine Søholm Hansen1Anna eStarnawska2Manuel eMattheisen3Manuel eMattheisen4Manuel eMattheisen5Anders Dupont Børglum6Anders Dupont Børglum7Anders Dupont Børglum8Henriette Nørmølle Buttenschøn9Henriette Nørmølle Buttenschøn10Mads eHollegaard11Aarhus University Hospital, Center of Child and Adolescent Psychiatry, BUC, RisskovDepartment of Congenital Diseases, Neonatal Genetics, Statens Serum InstitutDepartment of Biomedicine, Aarhus UniversityDepartment of Biomedicine, Aarhus UniversityThe Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCHCentre for Integrative Sequencing, iSEQDepartment of Biomedicine, Aarhus UniversityThe Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCHCentre for Integrative Sequencing, iSEQThe Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH6Translational Neuropsychiatry Unit (TNU), Institute for Clinical Medicine, Aarhus UniversityDepartment of Congenital Diseases, Neonatal Genetics, Statens Serum InstitutObsessive-compulsive disorder (OCD) is a neuropsychiatric disorder. Non-genetic factors and their interaction with genes have attracted increasing attention. Epigenetics is regarded an important interface between environmental signals and activation/repression of genomic responses. Epigenetic mechanisms have not previously been examined in OCD in children and adolescents.The aim of the present study was to examine the DNA methylation profile of selected genes in blood spots from neonates later diagnosed with OCD and in the same children/adolescents at the time of diagnosis compared with age- and sex matched controls. Furthermore, we wanted to characterize the association of the differential methylation profiles with the severity of OCD and treatment outcome.Dried and new blood spot samples were obtained from 21 female children/adolescents with verified OCD and 12 female controls. The differential methylation was analyzed using a linear model and the correlation with the severity of OCD and treatment outcome was analyzed using the Pearson correlation. We evaluated selected Illumina Infinium HumanMethylation450 BeadChip probes within and up to 100,000 bp up- and downstream of 14 genes previously associated with OCD (SLC1A1, SLC25A12, GABBR1, GAD1, DLGAP1, MOG, BDNF, OLIG2, NTRK2 and 3, ESR1, SL6A4, TPH2 and COMT).The study found no significantly differential methylation. However, preliminary support for a difference was found for the gamma-aminobutyric acid (GABA) B receptor 1 (cg10234998, cg17099072) in blood samples at birth and for the estrogen receptor 1 (ESR1) (cg10939667), the myelin oligodendrocyte glycoprotein (MOG) (cg16650906), and the brain-derived neurotrophic factor (BDNF) (cg14080521) in blood samples at the time of diagnosis.Preliminary support for an association was observed between the methylation profiles of GABBR1 and MOG and baseline severity, treatment effect, and responder status; and between the methylation profile of ESR1 and baseline severity. To our knowledge, this is the first study to examine the DNA methylation profiles in OCD. The study points towards possible differences in the methylation profiles and suggests a correlation with the severity of OCD. However, the results warrant further studies in larger sample sets.http://journal.frontiersin.org/Journal/10.3389/fpsyt.2016.00035/fullepigeneticsChildrenObsessive Compulsive DisorderadolescentsOCDMyelin oligodendrocyte glycoprotein (MOG)
collection DOAJ
language English
format Article
sources DOAJ
author Judith Becker Nissen
Christine Søholm Hansen
Anna eStarnawska
Manuel eMattheisen
Manuel eMattheisen
Manuel eMattheisen
Anders Dupont Børglum
Anders Dupont Børglum
Anders Dupont Børglum
Henriette Nørmølle Buttenschøn
Henriette Nørmølle Buttenschøn
Mads eHollegaard
spellingShingle Judith Becker Nissen
Christine Søholm Hansen
Anna eStarnawska
Manuel eMattheisen
Manuel eMattheisen
Manuel eMattheisen
Anders Dupont Børglum
Anders Dupont Børglum
Anders Dupont Børglum
Henriette Nørmølle Buttenschøn
Henriette Nørmølle Buttenschøn
Mads eHollegaard
DNA methylation at the neonatal state and at the time of diagnosis. Preliminary support for an association with the estrogen receptor 1, gamma-aminobutyric acid B receptor 1, and myelin oligodendrocyte glycoprotein in female adolescent patients with OCD
Frontiers in Psychiatry
epigenetics
Children
Obsessive Compulsive Disorder
adolescents
OCD
Myelin oligodendrocyte glycoprotein (MOG)
author_facet Judith Becker Nissen
Christine Søholm Hansen
Anna eStarnawska
Manuel eMattheisen
Manuel eMattheisen
Manuel eMattheisen
Anders Dupont Børglum
Anders Dupont Børglum
Anders Dupont Børglum
Henriette Nørmølle Buttenschøn
Henriette Nørmølle Buttenschøn
Mads eHollegaard
author_sort Judith Becker Nissen
title DNA methylation at the neonatal state and at the time of diagnosis. Preliminary support for an association with the estrogen receptor 1, gamma-aminobutyric acid B receptor 1, and myelin oligodendrocyte glycoprotein in female adolescent patients with OCD
title_short DNA methylation at the neonatal state and at the time of diagnosis. Preliminary support for an association with the estrogen receptor 1, gamma-aminobutyric acid B receptor 1, and myelin oligodendrocyte glycoprotein in female adolescent patients with OCD
title_full DNA methylation at the neonatal state and at the time of diagnosis. Preliminary support for an association with the estrogen receptor 1, gamma-aminobutyric acid B receptor 1, and myelin oligodendrocyte glycoprotein in female adolescent patients with OCD
title_fullStr DNA methylation at the neonatal state and at the time of diagnosis. Preliminary support for an association with the estrogen receptor 1, gamma-aminobutyric acid B receptor 1, and myelin oligodendrocyte glycoprotein in female adolescent patients with OCD
title_full_unstemmed DNA methylation at the neonatal state and at the time of diagnosis. Preliminary support for an association with the estrogen receptor 1, gamma-aminobutyric acid B receptor 1, and myelin oligodendrocyte glycoprotein in female adolescent patients with OCD
title_sort dna methylation at the neonatal state and at the time of diagnosis. preliminary support for an association with the estrogen receptor 1, gamma-aminobutyric acid b receptor 1, and myelin oligodendrocyte glycoprotein in female adolescent patients with ocd
publisher Frontiers Media S.A.
series Frontiers in Psychiatry
issn 1664-0640
publishDate 2016-03-01
description Obsessive-compulsive disorder (OCD) is a neuropsychiatric disorder. Non-genetic factors and their interaction with genes have attracted increasing attention. Epigenetics is regarded an important interface between environmental signals and activation/repression of genomic responses. Epigenetic mechanisms have not previously been examined in OCD in children and adolescents.The aim of the present study was to examine the DNA methylation profile of selected genes in blood spots from neonates later diagnosed with OCD and in the same children/adolescents at the time of diagnosis compared with age- and sex matched controls. Furthermore, we wanted to characterize the association of the differential methylation profiles with the severity of OCD and treatment outcome.Dried and new blood spot samples were obtained from 21 female children/adolescents with verified OCD and 12 female controls. The differential methylation was analyzed using a linear model and the correlation with the severity of OCD and treatment outcome was analyzed using the Pearson correlation. We evaluated selected Illumina Infinium HumanMethylation450 BeadChip probes within and up to 100,000 bp up- and downstream of 14 genes previously associated with OCD (SLC1A1, SLC25A12, GABBR1, GAD1, DLGAP1, MOG, BDNF, OLIG2, NTRK2 and 3, ESR1, SL6A4, TPH2 and COMT).The study found no significantly differential methylation. However, preliminary support for a difference was found for the gamma-aminobutyric acid (GABA) B receptor 1 (cg10234998, cg17099072) in blood samples at birth and for the estrogen receptor 1 (ESR1) (cg10939667), the myelin oligodendrocyte glycoprotein (MOG) (cg16650906), and the brain-derived neurotrophic factor (BDNF) (cg14080521) in blood samples at the time of diagnosis.Preliminary support for an association was observed between the methylation profiles of GABBR1 and MOG and baseline severity, treatment effect, and responder status; and between the methylation profile of ESR1 and baseline severity. To our knowledge, this is the first study to examine the DNA methylation profiles in OCD. The study points towards possible differences in the methylation profiles and suggests a correlation with the severity of OCD. However, the results warrant further studies in larger sample sets.
topic epigenetics
Children
Obsessive Compulsive Disorder
adolescents
OCD
Myelin oligodendrocyte glycoprotein (MOG)
url http://journal.frontiersin.org/Journal/10.3389/fpsyt.2016.00035/full
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