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Published Online: 1 April 2008

Schizophrenia Host Vulnerability and Risk of Metabolic Disturbances During Treatment with Antipsychotics

Abstract

People with schizophrenia die prematurely from comorbid physical diseases, particularly from cardiometabolic disturbances. Although some host vulnerability exists, there is also mounting evidence of a relationship between metabolic disturbances and antipsychotic medications. Clinicians must now make a careful appraisal of these risks when choosing an antipsychotic drug. Additionally, clinicians are required to undertake close monitoring for metabolic disturbances during antipsychotic therapy. Although switching antipsychotic medications is currently the preferred strategy if metabolic disturbances occur, there are other pharmacologic and nonpharmacologic approaches that might also prove beneficial for the individual patient. Metabolic disturbance and the detection and management thereof currently hold “center stage” in the psychopharmacology of schizophrenia.

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Published online: 1 April 2008
Published in print: Spring 2008

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Brian Miller, M.D., M.P.H.

Notes

Address correspondence to Peter F. Buckley, M.D., Professor and Chair, Department of Psychiatry and Health Behavior, Medical College of Georgia, 997 St. Sebastian Way, Augusta, GA 30912; e-mail, [email protected].

Funding Information

CME Disclosure
Peter F. Buckley, M.D., Department of Psychiatry, Medical College of Georgia, Augusta, GA.
Consultant: Abbott, AstraZeneca, BMS, Eli Lilly, Janssen, Pfizer, Merck, Roche Laboratories, Solvay, Wyeth. Grant/Research Support: AstraZeneca, BMS, Eli Lilly, Janssen, Pfizer, Solvay, Wyeth. Speakers Bureau: Abbott, BMS, AstraZeneca, Eli LIlly, Janssen.
Adriana Foster, M.D., Department of Psychiatry, Medical College of Georgia, Augusta, GA.
No relevant financial relationships to disclose.
Brian Miller, M.D., M.P.H., Department of Psychiatry, Medical College of Georgia, Augusta, GA. No relevant financial relationships to disclose.

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