Epigenetic mechanisms and stress coping in mood disorders

Introduction Experimental data from both clinical and preclinical studies have unequivocally shown positive correlations between stress and depression, stress, depression and epigenetic changes. Objectives The aim of this research is to analyze clinical trials on coping mechanisms and their intera...

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Main Authors: L. Hogea, A.M. Ulucean, L. Nussbaum
Format: Article
Language:English
Published: Cambridge University Press 2022-06-01
Series:European Psychiatry
Subjects:
Online Access:https://www.cambridge.org/core/product/identifier/S0924933822005508/type/journal_article
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author L. Hogea
A.M. Ulucean
L. Nussbaum
author_facet L. Hogea
A.M. Ulucean
L. Nussbaum
author_sort L. Hogea
collection DOAJ
description Introduction Experimental data from both clinical and preclinical studies have unequivocally shown positive correlations between stress and depression, stress, depression and epigenetic changes. Objectives The aim of this research is to analyze clinical trials on coping mechanisms and their interaction with epigenetic mechanisms in patients with mood disorders. Generally, we studied the interaction between these two mechanisms and its effects on the onset, recurrence and progression of these disorders. Methods 109 articles were analyzed, of which 37 were considered relevant. 72 studies were excluded based on titles and abstracts. Regarding the coping mechanisms, 10 longitudinal and cross-sectional studies were selected. Longitudinal studies are defined here by a follow-up period longer than 6 months. Results There is a consistent association in the literature between the degree of methylation of the NR3C1 gene, stress and affectivity disorders. The analyzed studies showed that methylation of the NR3C1 gene is associated with both stress and mood disorders. FKBP5 influences glucocorticoid receptor sensitivity and stress response. SLC6A4 gene methylation has been systematically associated with stress and affectivity disorders. Higher BDNF methylation has also been found in people who report high levels of stress at work. The data collected suggest that SKA2 methylation may serve as a biomarker for certain features of depression, such as suicidal ideation, and is not directly involved in the etiology of mood disorders. Conclusions The results suggest that environmental stress and adversity in early childhood may change biological systems through epigenetic mechanisms and have long-term consequences, increasing the risk for unfavorable prognosis of mood disorders. Disclosure No significant relationships.
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spelling doaj.art-5570ccb6c0f4482295a2d5705e17e6882023-11-17T05:09:19ZengCambridge University PressEuropean Psychiatry0924-93381778-35852022-06-0165S211S21110.1192/j.eurpsy.2022.550Epigenetic mechanisms and stress coping in mood disordersL. Hogea0A.M. Ulucean1L. Nussbaum2“Victor Babes” University of Medicine and Pharmacy, Department Of Neurosciences, Timisoara, Romania“Victor Babes” University of Medicine and Pharmacy, Department Of Neurosciences, Timisoara, Romania“Victor Babes” University of Medicine and Pharmacy, Department Of Neurosciences, Timisoara, Romania Introduction Experimental data from both clinical and preclinical studies have unequivocally shown positive correlations between stress and depression, stress, depression and epigenetic changes. Objectives The aim of this research is to analyze clinical trials on coping mechanisms and their interaction with epigenetic mechanisms in patients with mood disorders. Generally, we studied the interaction between these two mechanisms and its effects on the onset, recurrence and progression of these disorders. Methods 109 articles were analyzed, of which 37 were considered relevant. 72 studies were excluded based on titles and abstracts. Regarding the coping mechanisms, 10 longitudinal and cross-sectional studies were selected. Longitudinal studies are defined here by a follow-up period longer than 6 months. Results There is a consistent association in the literature between the degree of methylation of the NR3C1 gene, stress and affectivity disorders. The analyzed studies showed that methylation of the NR3C1 gene is associated with both stress and mood disorders. FKBP5 influences glucocorticoid receptor sensitivity and stress response. SLC6A4 gene methylation has been systematically associated with stress and affectivity disorders. Higher BDNF methylation has also been found in people who report high levels of stress at work. The data collected suggest that SKA2 methylation may serve as a biomarker for certain features of depression, such as suicidal ideation, and is not directly involved in the etiology of mood disorders. Conclusions The results suggest that environmental stress and adversity in early childhood may change biological systems through epigenetic mechanisms and have long-term consequences, increasing the risk for unfavorable prognosis of mood disorders. Disclosure No significant relationships. https://www.cambridge.org/core/product/identifier/S0924933822005508/type/journal_articlemood disordersstresscopingepigenetic
spellingShingle L. Hogea
A.M. Ulucean
L. Nussbaum
Epigenetic mechanisms and stress coping in mood disorders
European Psychiatry
mood disorders
stress
coping
epigenetic
title Epigenetic mechanisms and stress coping in mood disorders
title_full Epigenetic mechanisms and stress coping in mood disorders
title_fullStr Epigenetic mechanisms and stress coping in mood disorders
title_full_unstemmed Epigenetic mechanisms and stress coping in mood disorders
title_short Epigenetic mechanisms and stress coping in mood disorders
title_sort epigenetic mechanisms and stress coping in mood disorders
topic mood disorders
stress
coping
epigenetic
url https://www.cambridge.org/core/product/identifier/S0924933822005508/type/journal_article
work_keys_str_mv AT lhogea epigeneticmechanismsandstresscopinginmooddisorders
AT amulucean epigeneticmechanismsandstresscopinginmooddisorders
AT lnussbaum epigeneticmechanismsandstresscopinginmooddisorders