Paternal Age Effect: Replication in Schizophrenia With Intriguing Dissociation Between Bipolar With and Without Psychosis

Authors

Douglas S. Lehrer, Wright State University - Main CampusFollow
Michele T. Pato, State University of New York
Ramzi W. Nahhas, Wright State University - Main CampusFollow
Brian R. Miller, Medical College of Georgia
Dolores Malaspina, New York University
Peter F. Buckley, Medical College of Georgia
Janet L. Sobell, University of Southern California
Julie Walsh-Messinger, The Icahn School of Medicine at Mt. Sinai
Carlos N. Pato, State University of New York
Abbott, University of Southern California
Maria Helena Azevedo, University of Coimbra
Evelyn J. Bromet, State University of New York
Michael A. Escamilla, Texas Tech University Health Sciences Center
Ayman H. Fanous, Veterans Affairs Central Office
Laura J. Fochtmann, State University of New York
Becky Kinkead, Emory University
James A. Knowles, University of Southern California
Fabio Macciardi, Department of Psychiatry
Antonio Macedo, University of Coimbra
Stephen R. Marder, Department of Psychiatry
Steven A. McCarroll, Harvard Medical School
Helena Medeiros, Department of Psychiatry and the Behavioral Sciences
Christopher P. Morley, The State University of New York
Humberto Nicolini, Carracci Medical Group
Jeffrey J. Rakofsky, Emory University
Mark H. Rapaport, Emory University
Diana O. Perkins, University of North Carolina School of Medicine
Pamela Sklar, The Icahn School of Medicine at Mt. Sinai
Jordan W. Smoller, Harvard Medical School
Marquis Vawter, University of California, Irvine
Genomic Psychiatry Cohort Consortium

Document Type

Article

Publication Date

6-1-2016

Identifier/URL

43007184 (Pure); 26183902 (PubMed)

Abstract

Advanced paternal age (APA) is a risk factor for schizophrenia (Sz) and bipolar disorder (BP). Putative mechanisms include heritable genetic factors, de novo mutations, and epigenetic mechanisms. Few studies have explored phenotypic features associated with APA. The Genomic Psychiatry Cohort established a clinically characterized repository of genomic samples from subjects with a Sz-BP diagnosis or unaffected controls, 12,975 with parental age information. We estimated relative risk ratios for Sz, schizoaffective depressed and bipolar types (SA-D, SA-B), and BP with and without history of psychotic features (PF) relative to the control group, comparing each paternal age group to the reference group 20-24 years. All tests were two-sided with adjustment for multiple comparisons. Subjects with fathers age 45+ had significantly higher risk for all diagnoses except for BP w/o PF. APA also bore no significant relation to family psychiatric history. In conclusion, we replicated APA as a risk factor for Sz. To our knowledge, this is the first published report of APA in a BP sample stratified by psychosis history, extending this association only in BP w/PF. This suggests that phenotypic expression of the APA effect in Sz-BP spectrum is psychosis, per se, rather than other aspects of these complex disorders. The lack of a significant relationship between paternal age and familial disease patterns suggests that underlying mechanisms of the paternal age effect may involve a complex interaction of heritable and non-heritable factors. The authors discuss implications and testable hypotheses, starting with a focus on genetic mechanisms and endophenotypic expressions of dopaminergic function.

Comments

Publisher Copyright: © 2016 Wiley Periodicals, Inc.

DOI

10.1002/ajmg.b.32334

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