Literature DB >> 31683097

Investigation of MORC1 DNA methylation as biomarker of early life stress and depressive symptoms.

Mara Thomas1, Andressa Coope2, Carolin Falkenberg3, Boadie W Dunlop4, Darina Czamara5, Nadine Provencal2, W Edward Craighead4, Helen S Mayberg6, Charles B Nemeroff7, Elisabeth B Binder5, Vanessa Nieratschker3.   

Abstract

Early life stress (ELS) is associated with an increased risk of depression and this association may be mediated by epigenetic mechanisms. A previous epigenome-wide DNA methylation (DNAm) study investigating human newborns and two animal models of ELS suggested that the epigenetic regulator MORC1 is differentially methylated following ELS. The ELS-induced DNAm alterations were long-lasting in the animal models. However, whether this finding is also transferable to humans experiencing ELS in childhood was not investigated. Further, MORC1 may provide a link between ELS and adult depression, as MORC1 DNAm and genetic variants were found to be associated with depressive symptoms in humans. In the present study, we investigated the validity of MORC1 DNAm as a biomarker of ELS in humans and its role in linking ELS to depression later in life by studying childhood maltreatment. We analyzed whole blood MORC1 DNAm in an adult cohort (N = 151) that was characterized for both the presence of depressive symptoms and childhood maltreatment. Further, we investigated the association between MORC1 DNAm, depressive symptoms and childhood maltreatment in two additional cohorts (N = 299, N = 310). Overall, our data do not indicate an association of MORC1 DNAm with childhood maltreatment. An association of MORC1 DNAm with depressive symptoms was present in all cohorts, but was inconsistent in the specific CpG sites associated and the direction of effect (Tuebingen cohort: standardized β = 0.16, unstandardized β = 0.01, 95% CI [-0.0004, -0.0179], p = 0.061, PReDICT cohort: standardized β = -0.12, unstandardized β = -0.01, 95% CI [-0.0258, -0.0003], p = 0.045), Grady cohort: standardized β = 0.16, unstandardized β = 0.008, 95% CI [0.0019, 0.0143], p = 0.01). Our study thus suggests that peripheral MORC1 DNAm cannot serve as biomarker of childhood maltreatment in adults, but does provide further indication for the association of MORC1 DNAm with depressive symptoms.
Copyright © 2019 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Childhood trauma; DNA methylation; Depression; Early life stress; Epigenetics

Year:  2019        PMID: 31683097      PMCID: PMC6866669          DOI: 10.1016/j.jpsychires.2019.10.019

Source DB:  PubMed          Journal:  J Psychiatr Res        ISSN: 0022-3956            Impact factor:   4.791


  4 in total

1.  Maternal separation in rats induces neurobiological and behavioral changes on the maternal side.

Authors:  Ibrahim Bölükbas; Annakarina Mundorf; Nadja Freund
Journal:  Sci Rep       Date:  2020-12-31       Impact factor: 4.379

Review 2.  A systematic review of childhood maltreatment and DNA methylation: candidate gene and epigenome-wide approaches.

Authors:  Stephanie H Parade; Lindsay Huffhines; Nicole R Nugent; Audrey R Tyrka; Teresa E Daniels; Laura R Stroud
Journal:  Transl Psychiatry       Date:  2021-02-19       Impact factor: 6.222

3.  Metabolomics Based on Peripheral Blood Mononuclear Cells to Dissect the Mechanisms of Chaigui Granules for Treating Depression.

Authors:  Dehua Huang; Liwen Wang; Yanfei Wu; Xuemei Qin; Guanhua Du; Yuzhi Zhou
Journal:  ACS Omega       Date:  2022-03-07

4.  Morc1 as a potential new target gene in mood regulation: when and where to find in the brain.

Authors:  Annakarina Mundorf; Jennifer Koch; Nadja Kubitza; Selina C Wagner; Michaela Schmidt; Peter Gass; Nadja Freund
Journal:  Exp Brain Res       Date:  2021-07-30       Impact factor: 1.972

  4 in total

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