Publication

Parental type 2 diabetes in patients with non-affective psychosis

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Last modified
  • 02/25/2025
Type of Material
Authors
    Brian J. Miller, Augusta UniversityDavid Goldsmith, Emory UniversityNina Paletta, Augusta UniversityJoyce Wong, Augusta UniversityPrianka Kandhal, Augusta UniversityCarmen Black, Augusta UniversityMark Rapaport, Emory UniversityPeter F. Buckley, Augusta University
Language
  • English
Date
  • 2016-05-04
Publisher
  • Elsevier
Publication Version
Copyright Statement
  • © 2016 Elsevier B.V.
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 0920-9964
Volume
  • 175
Issue
  • 1-3
Start Page
  • 223
End Page
  • 225
Grant/Funding Information
  • In the past 12 months, Dr. Goldsmith received grant funding from the APIRE-Janssen Resident Research Award and the Janssen Academic Research Mentoring program.
  • Dr. Buckley has nothing to disclose relevant to the present work. In the past 12months, received grant/research support for fromtheAmerican Psychiatric Association fromthe National Institute of Mental Health, Janssen Pharmaceutica, Pfizer, and Sunovion,
  • Dr. Miller received grant support for this study from the National Institute of Mental Health (K23MH098014)
  • Ms. Kandhal received funding from the Augusta University Dean's Medical Scholars program
  • Ms. Wong received funding from the Augusta University Dean's Medical Scholars program.
  • Dr. Black received funding from the Augusta University Dean's Medical Scholars program.
  • Ms. Paletta received funding from the Augusta University Dean's Medical Scholars program.
Abstract
  • Objective: People with schizophrenia have an increased risk of diabetes that may be independent of antipsychotics. Previous studies have explored the prevalence of a family history of type 2 diabetes (DM2) in schizophrenia. We hypothesized that parental DM2 is increased in probands with non-affective psychosis (NAP) compared to controls, and parental DM2 predicts comorbid diabetes in NAP, after controlling for potential confounders. Method: N = 217 patients with NAP and N = 67 controls were interviewed for a history of parental DM2. NAP was investigated as a predictor of parental DM2 in binary logistic regression models, controlling for age, sex, race, smoking, body mass index, socioeconomic status, and parental psychiatric history. Results: There was an increased prevalence of DM2 in the mother (30.0% vs 13.8%, p = 0.013) and in either the mother or father (44.5% vs 24.6%, p = 0.006) in patients with NAP versus controls. After accounting for potential confounders, NAP was associated with significant increased odds of parental DM2 (OR = 2.80, 95% CI 1.08-7.23, p = 0.034). Parental DM2 was also associated with increased odds of comorbid DM2 in NAP (OR = 3.67, 95% CI 1.58-8.56, p = 0.003). Conclusions: We replicated an association of an increased prevalence of parental DM2 in patients with NAP. Parental DM2 was also an independent predictor of comorbid DM2 in these patients. These associations may be due to shared environmental or genetic risk factors, or gene by environment interactions. Given risks of incident diabetes with antipsychotic treatment, screening for parental DM2 status is germane to the clinical care of patients with NAP.
Author Notes
  • *Corresponding Author: Brian J. Miller, MD, PhD, MPH, Department of Psychiatry and Health Behavior, Augusta University, 997 Saint Sebastian Way, Augusta, Georgia 30912, United States, Fax: +1-706-721-6602, Tel: +1-706-721-4445, Email: brmiller@gru.edu
Keywords
Research Categories
  • Health Sciences, Mental Health
  • Psychology, Behavioral
  • Health Sciences, Pathology

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