Inflammatory and Epigenetic Pathways for Perinatal Depression. (May 2016)

• Record Type: Journal Article
• Authors: Garfield, Lindsey; Mathews, Herbert L.; Janusek, Linda Witek
• Is Part Of: Biological research for nursing. Volume 18:Number 3(2016:May)
• Page Start: 331
• Page End: 343
• Publication Date: 2016-05
• Subjects: perinatal depression -- inflammation -- oxytocin -- epigenetics -- childhood adversity; Clinical biochemistry -- Periodicals; Physiology, Pathological -- Periodicals; Nursing -- Periodicals; Nursing -- Research -- Periodicals; 610.73
• DOI: 10.1177/1099800415614892
• Languages: English
• ISSNs: 1099-8004

Abstract

Depression during the perinatal period is common and can have adverse consequences for women and their children. Yet, the biobehavioral mechanisms underlying perinatal depression are not known. Adverse early life experiences increase the risk for adult depression. One potential mechanism by which this increased risk occurs is epigenetic embedding of inflammatory pathways. The purpose of this article is to propose a conceptual model that explicates the linkage between early life adversity and the risk for maternal depression. The model posits that early life adversity embeds a proinflammatory epigenetic signature (altered DNA methylation) that predisposes vulnerable women to depression during pregnancy and the postpartum period. As proposed, women with a history of early life adversity are more likely to exhibit higher levels of proinflammatory cytokines and lower levels of oxytocin in response to the demands of pregnancy and new motherhood, both of which are associated with the risk for perinatal depression. The model is designed to guide investigations into the biobehavioral basis for perinatal depression, with emphasis upon the impact of early life adversity. Testing this model will provide a better understanding of maternal depressive risk and improve identification of vulnerable women who would benefit from targeted interventions that can reduce the impact of perinatal depression on maternal–infant health.