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      Gene–Environment Interaction in Major Depression: Focus on Experience-Dependent Biological Systems

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          Abstract

          Major depressive disorder (MDD) is a multifactorial and polygenic disorder, where multiple and partially overlapping sets of susceptibility genes interact each other and with the environment, predisposing individuals to the development of the illness. Thus, MDD results from a complex interplay of vulnerability genes and environmental factors that act cumulatively throughout individual’s lifetime. Among these environmental factors, stressful life experiences, especially those occurring early in life, have been suggested to exert a crucial impact on brain development, leading to permanent functional changes that may contribute to lifelong risk for mental health outcomes. In this review, we will discuss how genetic variants (polymorphisms, SNPs) within genes operating in neurobiological systems that mediate stress response and synaptic plasticity, can impact, by themselves, the vulnerability risk for MDD; we will also consider how this MDD risk can be further modulated when gene × environment interaction is taken into account. Finally, we will discuss the role of epigenetic mechanisms, and in particular of DNA methylation and miRNAs expression changes, in mediating the effect of the stress on the vulnerability risk to develop MDD. Taken together, we aim to underlie the role of genetic and epigenetic processes involved in stress- and neuroplasticity-related biological systems on the development of MDD after exposure to early life stress, thereby building the basis for future research and clinical interventions.

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          Most cited references119

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          Origins and Mechanisms of miRNAs and siRNAs.

          Over the last decade, approximately 20-30 nucleotide RNA molecules have emerged as critical regulators in the expression and function of eukaryotic genomes. Two primary categories of these small RNAs--short interfering RNAs (siRNAs) and microRNAs (miRNAs)--act in both somatic and germline lineages in a broad range of eukaryotic species to regulate endogenous genes and to defend the genome from invasive nucleic acids. Recent advances have revealed unexpected diversity in their biogenesis pathways and the regulatory mechanisms that they access. Our understanding of siRNA- and miRNA-based regulation has direct implications for fundamental biology as well as disease etiology and treatment.
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            Gene silencing by microRNAs: contributions of translational repression and mRNA decay.

            Despite their widespread roles as regulators of gene expression, important questions remain about target regulation by microRNAs. Animal microRNAs were originally thought to repress target translation, with little or no influence on mRNA abundance, whereas the reverse was thought to be true in plants. Now, however, it is clear that microRNAs can induce mRNA degradation in animals and, conversely, translational repression in plants. Recent studies have made important advances in elucidating the relative contributions of these two different modes of target regulation by microRNAs. They have also shed light on the specific mechanisms of target silencing, which, although it differs fundamentally between plants and animals, shares some common features between the two kingdoms.
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              Adverse childhood experiences and the risk of depressive disorders in adulthood.

              Research examining the association between childhood abuse and depressive disorders has frequently assessed abuse categorically, thus not permitting discernment of the cumulative impact of multiple types of abuse. As previous research has documented that adverse childhood experiences (ACEs) are highly interrelated, we examined the association between the number of such experiences (ACE score) and the risk of depressive disorders. Retrospective cohort study of 9460 adult health maintenance organization members in a primary care clinic in San Diego, CA who completed a survey addressing a variety of health-related concerns, which included standardized assessments of lifetime and recent depressive disorders, childhood abuse and household dysfunction. Lifetime prevalence of depressive disorders was 23%. Childhood emotional abuse increased risk for lifetime depressive disorders, with adjusted odds ratios (ORs) of 2.7 [95% confidence interval (CI), 2.3-3.2] in women and 2.5 (95% CI, 1.9-3.2) in men. We found a strong, dose-response relationship between the ACE score and the probability of lifetime and recent depressive disorders (P<0.0001). This relationship was attenuated slightly when a history of growing up with a mentally ill household member was included in the model, but remained significant (P<0.001). The number of ACEs has a graded relationship to both lifetime and recent depressive disorders. These results suggest that exposure to ACEs is associated with increased risk of depressive disorders up to decades after their occurrence. Early recognition of childhood abuse and appropriate intervention may thus play an important role in the prevention of depressive disorders throughout the life span.
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                Author and article information

                Contributors
                URI : http://frontiersin.org/people/u/202815
                URI : http://frontiersin.org/people/u/95091
                URI : http://frontiersin.org/people/u/222250
                URI : http://frontiersin.org/people/u/181031
                URI : http://frontiersin.org/people/u/201670
                URI : http://frontiersin.org/people/u/14856
                URI : http://frontiersin.org/people/u/155218
                URI : http://frontiersin.org/people/u/96224
                Journal
                Front Psychiatry
                Front Psychiatry
                Front. Psychiatry
                Frontiers in Psychiatry
                Frontiers Media S.A.
                1664-0640
                08 May 2015
                2015
                : 6
                : 68
                Affiliations
                [1] 1IRCCS Fatebenefratelli San Giovanni di Dio , Brescia, Italy
                [2] 2Faculty of Psychology, eCampus University , Novedrate, Como, Italy
                [3] 3Department of Psychiatry and Neuroscience Program, McLean Hospital, Harvard Medical School , Belmont, MA, USA
                [4] 4Stress, Psychiatry and Immunology Laboratory, Department of Psychological Medicine, Institute of Psychiatry, King’s College London , London, UK
                [5] 5Department of Pharmacological and Biomolecular Sciences, University of Milan , Milan, Italy
                Author notes

                Edited by: Bruno Etain, University Paris East, France

                Reviewed by: Vaibhav A. Diwadkar, Wayne State University School of Medicine, USA; Bernhard J. Mitterauer, Volitronics-Institute for Basic Research Psychopathology and Brain Philosophy, Austria

                *Correspondence: Annamaria Cattaneo, Stress, Psychiatry and Immunology Laboratory, Department of Psychological Medicine, Institute of Psychiatry, King’s College London, Coldharbour Lane, London SE5 9NU, UK, annamaria.cattaneo@ 123456kcl.ac.uk ; acattaneo@ 123456fatebenefratelli.it

                Specialty section: This article was submitted to Schizophrenia, a section of the journal Frontiers in Psychiatry

                Article
                10.3389/fpsyt.2015.00068
                4424810
                26005424
                a4101ad9-4814-478b-9d2b-7f2c1af75224
                Copyright © 2015 Lopizzo, Bocchio Chiavetto, Cattane, Plazzotta, Tarazi, Pariante, Riva and Cattaneo.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 29 December 2014
                : 21 April 2015
                Page count
                Figures: 0, Tables: 2, Equations: 0, References: 153, Pages: 12, Words: 11060
                Funding
                Funded by: Medical Research Council (UK)
                Award ID: MR/J002739/1
                Funded by: Psychiatry Research Trust, UK
                Award ID: McGregor 97
                Funded by: Commission of European Communities Seventh Framework Programme
                Award ID: 22963
                Funded by: National Institute for Health Research Biomedical Research Centre in Mental Health at South London
                Funded by: Maudsley NHS Foundation Trust and King’s College London
                Funded by: Italian Ministry of Health
                Funded by: Italian Ministry of University and Research
                Award ID: PRIN 20107MSMA4
                Funded by: Fondazione CARIPLO
                Award ID: 2012-0503
                Funded by: European Union/ERANET
                Funded by: Cariplo Foundation
                Award ID: 2009-2701
                Funded by: Italian Ministry of Health
                Categories
                Psychiatry
                Review

                Clinical Psychology & Psychiatry
                vulnerability genes,stressful life events,dna methylation,mirnas,depression

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