Publication

Depression Predicts Global Functional Outcomes in Individuals at Clinical High Risk for Psychosis

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Last modified
  • 07/08/2025
Type of Material
Authors
    Wisteria Deng, Yale UniversityJean Addington, Hotchkiss Brain InstituteCarrie E Bearden, University of California, Los AngelesKristin S Cadenhead, University of California, San DiegoBarbara A Cornblatt, Zucker Hillside HospitalDaniel H Mathalon, UCSF, SFVA Medical CenterThomas H McGlashan, Yale UniversityDiana O Perkins, University of North CarolinaLarry J Seidman, Harvard Medical SchoolMing T Tsuang, University of California, San DiegoScott W Woods, Yale UniversityElaine Walker, Emory UniversityJutta Joormann, Yale UniversityTyrone Cannon, Yale University
Language
  • English
Date
  • 2021-11-17
Publisher
  • Wiley Periodicals LLC
Publication Version
Copyright Statement
  • © 2021 The Authors. Psychiatric Research and Clinical Practice published by Wiley Periodicals LLC on behalf of American Psychiatric Association
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Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 3
Issue
  • 4
Start Page
  • 163
End Page
  • 171
Supplemental Material (URL)
Abstract
  • Objectives While co‐morbid depression is associated with poor functional outcome among patients with schizophrenia, whether depression similarly predicts poorer outcomes in individuals at clinical high‐risk for psychosis (CHR‐P) is not clear. The present study aimed to examine depressive symptoms in relation to long‐term global functional outcomes in the North American Prodrome Longitudinal Study cohort (NAPLS2). Methods CHR individuals were evaluated clinically at baseline and at 12‐ and 24‐month follow‐ups for depressive and prodromal symptom severity as well as general functioning. Regression models were built to investigate whether baseline positive and depressive symptom scores predicted longitudinal improvement in global functioning. Results A total of 406 CHR individuals completed the 12‐month follow‐up assessment and 259 CHR individuals completed the 24‐month assessment. Baseline depressive symptoms in the CHR‐P population were found to predict better global functional outcomes at 2 years. Furthermore, the degree of recovery of depressive symptoms in the first year following baseline completely mediated the association between depressive symptoms at baseline and functional improvement at 2 years. Conclusions Presence of affective symptoms within the CHR‐P population has different implications for prognosis compared with patients with schizophrenia. The present findings support the view that among those at risk for psychosis, depressive symptoms at baseline predict a more favorable course of functional recovery, and highlight the potential importance of treating co‐occurring depressive symptoms at an early stage of psychosis risk.
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Research Categories
  • Health Sciences, Mental Health

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