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Published Online: 1 January 2011

The Structure of Genetic and Environmental Risk Factors for Syndromal and Subsyndromal Common DSM-IV Axis I and All Axis II Disorders

Abstract

Objective:

The authors sought to clarify the structure of the genetic and environmental risk factors for 22 DSM-IV disorders: 12 common axis I disorders and all 10 axis II disorders.

Method:

The authors examined syndromal and subsyndromal axis I diagnoses and five categories reflecting number of endorsed criteria for axis II disorders in 2,111 personally interviewed young adult members of the Norwegian Institute of Public Health Twin Panel.

Results:

Four correlated genetic factors were identified: axis I internalizing, axis II internalizing, axis I externalizing, and axis II externalizing. Factors 1 and 2 and factors 3 and 4 were moderately correlated, supporting the importance of the internalizing-externalizing distinction. Five disorders had substantial loadings on two factors: borderline personality disorder (factors 3 and 4), somatoform disorder (factors 1 and 2), paranoid and dependent personality disorders (factors 2 and 4), and eating disorders (factors 1 and 4). Three correlated environmental factors were identified: axis II disorders, axis I internalizing disorders, and externalizing disorders versus anxiety disorders.

Conclusions:

Common axis I and II psychiatric disorders have a coherent underlying genetic structure that reflects two major dimensions: internalizing versus externalizing, and axis I versus axis II. The underlying structure of environmental influences is quite different. The organization of common psychiatric disorders into coherent groups results largely from genetic, not environmental, factors. These results should be interpreted in the context of unavoidable limitations of current statistical methods applied to this number of diagnostic categories.

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Information & Authors

Information

Published In

Go to American Journal of Psychiatry
Go to American Journal of Psychiatry
American Journal of Psychiatry
Pages: 29 - 39
PubMed: 20952461

History

Received: 8 March 2010
Revision received: 8 July 2010
Accepted: 15 July 2010
Published online: 1 January 2011
Published in print: January 2011

Authors

Details

Kenneth S. Kendler, M.D.
From the Virginia Institute for Psychiatric and Behavioral Genetics, the Department of Psychiatry, and the Department of Human and Molecular Genetics, Virginia Commonwealth University, Richmond; the Division of Mental Health, Norwegian Institute of Public Health, Oslo, Norway; the Institute of Psychiatry and the Institute of Psychology, University of Oslo; and the Department of Epidemiology, Columbia University, New York.
Steven H. Aggen, Ph.D.
From the Virginia Institute for Psychiatric and Behavioral Genetics, the Department of Psychiatry, and the Department of Human and Molecular Genetics, Virginia Commonwealth University, Richmond; the Division of Mental Health, Norwegian Institute of Public Health, Oslo, Norway; the Institute of Psychiatry and the Institute of Psychology, University of Oslo; and the Department of Epidemiology, Columbia University, New York.
Gun Peggy Knudsen, Ph.D.
From the Virginia Institute for Psychiatric and Behavioral Genetics, the Department of Psychiatry, and the Department of Human and Molecular Genetics, Virginia Commonwealth University, Richmond; the Division of Mental Health, Norwegian Institute of Public Health, Oslo, Norway; the Institute of Psychiatry and the Institute of Psychology, University of Oslo; and the Department of Epidemiology, Columbia University, New York.
Espen Røysamb, Ph.D.
From the Virginia Institute for Psychiatric and Behavioral Genetics, the Department of Psychiatry, and the Department of Human and Molecular Genetics, Virginia Commonwealth University, Richmond; the Division of Mental Health, Norwegian Institute of Public Health, Oslo, Norway; the Institute of Psychiatry and the Institute of Psychology, University of Oslo; and the Department of Epidemiology, Columbia University, New York.
Michael C. Neale, Ph.D.
From the Virginia Institute for Psychiatric and Behavioral Genetics, the Department of Psychiatry, and the Department of Human and Molecular Genetics, Virginia Commonwealth University, Richmond; the Division of Mental Health, Norwegian Institute of Public Health, Oslo, Norway; the Institute of Psychiatry and the Institute of Psychology, University of Oslo; and the Department of Epidemiology, Columbia University, New York.
Ted Reichborn-Kjennerud, M.D.
From the Virginia Institute for Psychiatric and Behavioral Genetics, the Department of Psychiatry, and the Department of Human and Molecular Genetics, Virginia Commonwealth University, Richmond; the Division of Mental Health, Norwegian Institute of Public Health, Oslo, Norway; the Institute of Psychiatry and the Institute of Psychology, University of Oslo; and the Department of Epidemiology, Columbia University, New York.

Notes

Address correspondence and reprint requests to Dr. Kendler, Virginia Commonwealth University, Virginia Institute for Psychiatric and Behavioral Genetics, Box 980126, Richmond, VA 23298-0126; [email protected] (e-mail).

Funding Information

The authors report no financial relationships with commercial interests.Supported in part by NIH grant MH-068643 and grants from the Norwegian Research Council, the Norwegian Foundation for Health and Rehabilitation, the Norwegian Council for Mental Health, and the European Commission under the program “Quality of Life and Management of the Living Resources” of the Fifth Framework Program (no. QLG2-CT-2002-01254).

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