Perspective
Neuropsychopharmacology (2004) 29, 641–648, advance online publication, 3 March 2004; doi:10.1038/sj.npp.1300397
Importance of Studying the Contributions of Early Adverse Experience to Neurobiological Findings in Depression
Christine Heim1, Paul M Plotsky1 and Charles B Nemeroff1
1Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, USA
Correspondence: Dr CB Nemeroff, Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, 1639 Pierce Drive, WMB, Suite 4000, Atlanta, GA 30322, USA. Tel: 404 727 8382; Fax: 404 727 3233; E-mail: cnemero@emory.edu
Received 14 July 2003; Revised 1 December 2003; Accepted 31 December 2003; Published online 3 March 2004.
Abstract
Almost four decades of intensive research have sought to elucidate the neurobiological bases of depression. Epidemiological studies have revealed that both genetic and environmental factors contribute to the risk for depression. Adverse early-life experiences influence neurobiological systems within genetic limits, leading to the neurobiological and behavioral manifestations of depression. We summarize the burgeoning evidence concerning a pre-eminent role of early adverse experience in the pathogenesis of depression. The available data suggest that (1) early adverse experience contributes to the pathophysiology of depression, (2) there are neurobiologically different subtypes of depression depending on the presence or absence of early adverse experience, likely having confounded previous research on the neurobiology of depression, and (3) early adverse experience likely influences treatment response in depression. Classification of depression based on developmental and neurobiological features will likely considerably improve future research in the field of depression, and might lead to optimized treatment strategies that directly target different neurobiological pathways to depression.
Keywords:
CRF, HPA axis, early life trauma, depression, anxiety
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