Plasticity of the epigenome during early-life stress

• Published in: Seminars in cell & developmental biology 2018-05, Vol.77, p.115-132
• Main Authors: Burns, S. Barnett, Szyszkowicz, J. Kasia, Luheshi, Giamal N., Lutz, Pierre-Eric, Turecki, Gustavo
• Format: Article
• Language: English
• Subjects: Age Factors; Animals; Brain-Derived Neurotrophic Factor - metabolism; Differential susceptibility; Disease Models, Animal; DNA Methylation - genetics; Early life adversity; Epigenesis, Genetic - genetics; Epigenetics; gamma-Aminobutyric Acid - metabolism; Glutamic Acid - metabolism; HPA axis; Humans; Hypothalamo-Hypophyseal System - physiology; Life Sciences; Mental Disorders - etiology; Mental Disorders - genetics; Mice; Pituitary-Adrenal System - physiology; Protein Processing, Post-Translational - genetics; Psychopathology; Rats; Resilience; Resilience, Psychological; RNA, Untranslated - genetics; Serotonin - metabolism; Signal Transduction - physiology; Stress, Psychological - genetics; Stress, Psychological - psychology
• ISSN: 1084-9521; 1096-3634
• DOI: 10.1016/j.semcdb.2017.09.033

Early life adversity remains a significant risk factor for the development of a host of negative behavioural and pathological outcomes in adulthood long after the stressor is over. Recent evidence indicates that these lasting effects of ELS may occur via alterations in the epigenetic landscape. Here, we review the main findings of the effects of early life adversity on DNA methylation, histone post-translational modification, and non-coding RNAs in the context of psychiatric disease in animal models and human cohorts. We specifically explore how early life adversity alters epigenetic patterns in both a global manner, and in specific candidate genes that play a role in relevant systems such as the hypothalamic-pituitary-adrenal axis, as well as neurotransmitter and neuroendocrine signalling. We also discuss how individual factors, such as genetics, sex, and age, as well as the type, and timing of early life adversity, can create differential susceptibility and significantly moderate outcomes. Although challenges remain in deciphering the complexity of how the early environment interacts with individual factors to determine epigenetic patterns, as well as how to translate these mechanistic findings into clinically relevant populations, the reviewed literature sheds light on the potential of the field to identify effective interventions for vulnerable individuals.