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Published Online: 20 February 2015

Triparental Families: A New Genetic-Epidemiological Design Applied to Drug Abuse, Alcohol Use Disorders, and Criminal Behavior in a Swedish National Sample

Abstract

Objective:

The authors sought to clarify the sources of parent-offspring resemblance for drug abuse, alcohol use disorders, and criminal behavior, using a novel genetic-epidemiological design.

Method:

Using national registries, the authors identified rates of drug abuse, alcohol use disorders, and criminal behavior in 41,360 Swedish individuals born between 1960 and 1990 and raised in triparental families comprising a biological mother who reared them, a “not-lived-with” biological father, and a stepfather.

Results:

When each syndrome was examined individually, hazard rates for drug abuse in offspring of parents with drug abuse were highest for mothers (2.80, 95% CI=2.23–3.38), intermediate for not-lived-with fathers (2.45, 95% CI=2.14–2.79), and lowest for stepfathers (1.99, 95% CI=1.55–2.56). The same pattern was seen for alcohol use disorders (2.23, 95% CI=1.93–2.58; 1.84, 95% CI=1.69–2.00; and 1.27, 95% CI=1.12–1.43) and criminal behavior (1.55, 95% CI=1.44–1.66; 1.46, 95% CI=1.40–1.52; and 1.30, 95% CI=1.23–1.37). When all three syndromes were examined together, specificity of cross-generational transmission was highest for mothers, intermediate for not-lived-with fathers, and lowest for stepfathers. Analyses of intact families and other not-lived-with parents and stepparents showed similar cross-generation transmission for these syndromes in mothers and fathers, supporting the representativeness of results from triparental families.

Conclusions:

A major strength of the triparental design is its inclusion, within a single family, of parents who provide, to a first approximation, their offspring with genes plus rearing, genes only, and rearing only. For drug abuse, alcohol use disorders, and criminal behavior, the results of this study suggest that parent-offspring transmission involves both genetic and environmental processes, with genetic factors being somewhat more important. These results should be interpreted in the context of the strengths and limitations of national registry data.

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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: 553 - 560
PubMed: 25698436

History

Received: 14 September 2014
Revision received: 27 October 2014
Revision received: 25 November 2014
Accepted: 30 November 2014
Published online: 20 February 2015
Published in print: June 01, 2015

Authors

Affiliations

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 Center for Primary Health Care Research, Lund University, Malmö, Sweden; and the Stanford Prevention Research Center, Stanford University School of Medicine, Stanford.
Henrik Ohlsson, 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 Center for Primary Health Care Research, Lund University, Malmö, Sweden; and the Stanford Prevention Research Center, Stanford University School of Medicine, Stanford.
Jan Sundquist, M.D., 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 Center for Primary Health Care Research, Lund University, Malmö, Sweden; and the Stanford Prevention Research Center, Stanford University School of Medicine, Stanford.
Kristina Sundquist, M.D., 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 Center for Primary Health Care Research, Lund University, Malmö, Sweden; and the Stanford Prevention Research Center, Stanford University School of Medicine, Stanford.

Notes

Address correspondence to Dr. Kendler ([email protected]).

Competing Interests

The authors report no financial relationships with commercial interests.

Funding Information

Swedish Research Council : 2012-2378, K2012-70X-15428-08-3
National Institutes of Health10.13039/100000002: RO1 DA030005
Ellison Medical Foundation10.13039/100000863:
Supported by NIAAA grant RO1AA023534, NIDA grant RO1 DA030005, the Ellison Medical Foundation, the Swedish Research Council (K2012-70X-15428-08-3 to Dr. K. Sundquist), the Swedish Research Council for Health, Working Life, and Welfare (Forte; Reg.nr. 2013-1836 to Dr. K. Sundquist), the Swedish Research Council (2012-2378 to Dr. J. Sundquist), and Agreement on Medical Training and Research (ALF) funding from Region Skåne awarded to Drs. Sundquist and Sundquist.

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