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Published Online: 1 December 2010

Personalized Medicine for Depression: Can We Match Patients With Treatments?

Abstract

Objective:

Response to specific depression treatments varies widely among individuals. Understanding and predicting that variation could have great benefits for people living with depression.

Method:

The authors describe a conceptual model for identifying and evaluating evidence relevant to personalizing treatment for depression. They review evidence related to three specific treatment decisions: choice between antidepressant medication and psychotherapy, selection of a specific antidepressant medication, and selection of a specific psychotherapy. They then discuss potential explanations for negative findings as well as implications for research and clinical practice.

Results:

Many previous studies have examined general predictors of outcome, but few have examined true moderators (predictors of differential response to alternative treatments). The limited evidence indicates that some specific clinical characteristics may inform the choice between antidepressant medication and psychotherapy and the choice of specific antidepressant medication. Research to date does not identify any biologic or genetic predictors of sufficient clinical utility to inform the choice between medication and psychotherapy, the selection of specific medication, or the selection of a specific psychotherapy.

Conclusions:

While individuals vary widely in response to specific depression treatments, the variability remains largely unpredictable. Future research should focus on identifying true moderator effects and should consider how response to treatments varies across episodes. At this time, our inability to match patients with treatments implies that systematic follow-up assessment and adjustment of treatment are more important than initial treatment selection.

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Information

Published In

Go to American Journal of Psychiatry
Go to American Journal of Psychiatry
American Journal of Psychiatry
Pages: 1445 - 1455
PubMed: 20843873

History

Received: 24 November 2009
Revision received: 9 February 2010
Revision received: 4 June 2010
Accepted: 14 June 2010
Published online: 1 December 2010
Published in print: December 2010

Authors

Affiliations

Gregory E. Simon, M.D., M.P.H.
From the Group Health Research Institute, Seattle; and the Laboratory of Psychiatric Pharmacogenomics, Massachusetts General Hospital, Boston.
Roy H. Perlis, M.D., M.Sc.
From the Group Health Research Institute, Seattle; and the Laboratory of Psychiatric Pharmacogenomics, Massachusetts General Hospital, Boston.

Notes

Address correspondence and reprint requests to Dr. Simon, Group Health Research Institute, 1730 Minor Ave., #1600, Seattle, WA 98101; [email protected] (e-mail).

Funding Information

Dr. Perlis has served as an advisory board member or received consulting or speaking fees from AstraZeneca, Bristol-Myers Squibb, Eli Lilly, Glaxo SmithKline, Proteus Biomedical, and Pfizer; he also holds equity and receives royalties from Concordant Rater Systems. Dr. Simon reports no financial relationships with commercial interests.Supported by National Institute of Mental Health grants P20MH-068572, R01MH-085930, and R01MH-086026.

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