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Issue 1071 coverPSYCHOBIOLOGY OF POSTTRAUMATIC STRESS DISORDER A Decade of Progress Volume 1071 published July 2006
Ann. N.Y. Acad. Sci. 1071: 379–396 (2006). doi: 10.1196/annals.1364.028
Copyright © 2006 by the New York Academy of Sciences
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Articles by YEHUDA, R.
Articles by CHARNEY, D. S.
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Articles by YEHUDA, R.
Articles by CHARNEY, D. S.

Developing an Agenda for Translational Studies of Resilience and Vulnerability Following Trauma Exposure

RACHEL YEHUDAa,b, JANINE D. FLORYa, STEVEN SOUTHWICKc AND DENNIS S. CHARNEYa

a Mount Sinai School of Medicine, New York, New York 10029, USA b James J. Peters Veterans Affairs Medical Center, Bronx, New York 10468, USA c Yale Medical School and Veterans Affairs Connecticut, West Haven, Connecticut 06510, USA

Key Words: resilience • PTSD • trauma • translational research • brain • neuroendocrine markers

Address for correspondence: Rachel Yehuda, Ph.D., Bronx VA OOMH, 130 West Kingsbridge Road, Bronx, NY 10468. Voice: 718-584-9000; ext.: 6964; fax: 718-741-4775.  e-mail: Rachel.Yehuda{at}med.va.gov

Here we outline a translational research agenda for studies of resilience, defined as the process of adapting well in the face of adversity or trauma. We argue that an individual differences approach to the study of resilience, in which the full range of behavioral and biological responses to stress exposure is examined can be applied across human samples (e.g., people who have developed psychopathology versus those who have not; people who have been exposed to trauma versus those who have not) and even, in some cases, across species. We delineate important psychological resilience-related factors including positive affectivity and optimism, cognitive flexibility, coping, social support, emotion regulation, and mastery. Key brain regions associated with stress-related psychopathology have been identified with animal models of fear (e.g., extinction and fear conditioning; memory reconsolidation) and we describe how these regions can be studied in humans using neuroimaging technology. Finally, we cite recent research identifying neuroendocrine markers of resilience and recovery in humans (e.g., neuropeptide Y [NPY], dehydroepiandrosterone [DHEA]) that can also be measured, in some cases, in other species. That exposure to adversity or trauma does not necessarily lead to impairment and the development of psychopathology in all people is an important observation. Understanding why this is so will provide clues for the development of therapeutic interventions for those people who do develop stress-related psychopathology, or even for the prevention of adverse outcomes.




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