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Association of Psychotic Experiences and Incident Depression in a Longitudinal Population‐Based Community Survey

OBJECTIVE: The present study aims to determine if psychotic experiences in a general population sample are a risk factor for depressive disorders at a 15‐year follow‐up visit. METHOD: A longitudinal population cohort of adults over age 18 from East Baltimore were followed from 1981 to 1996 with 1409...

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Autores principales: Rodriguez, Katrina M., Sharifi, Vandad, Eaton, William W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9997072/
https://www.ncbi.nlm.nih.gov/pubmed/36909140
http://dx.doi.org/10.1176/appi.prcp.20220021
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author Rodriguez, Katrina M.
Sharifi, Vandad
Eaton, William W.
author_facet Rodriguez, Katrina M.
Sharifi, Vandad
Eaton, William W.
author_sort Rodriguez, Katrina M.
collection PubMed
description OBJECTIVE: The present study aims to determine if psychotic experiences in a general population sample are a risk factor for depressive disorders at a 15‐year follow‐up visit. METHOD: A longitudinal population cohort of adults over age 18 from East Baltimore were followed from 1981 to 1996 with 1409 participants included in analyses. Delusions and hallucinations and depressive disorders were assessed using DSM‐III criteria. Odds ratios were obtained using logistic regression with psychotic experiences modeled both dichotomously and as count variables as predictors of major and minor depressive disorders at wave three. Age, race, and sex were included as covariates in the model. RESULTS: Both delusions and hallucinations were associated with an increased odds of incident depressive disorders. Delusions, but not hallucinations, were associated with increased odds of major depressive disorder (adjusted odds ratio, 3.04 [95% CI = 1.29–7.13]) and both delusions and hallucinations were associated with increased odds of minor depressive disorder (adjusted odds ratios, 4.6 [95% CI = 2.11–10.04] and 3.93 [95% CI = 2.11–7.32]). There was a dose‐response relationship in number of psychotic experiences reported and odds of depressive disorders. CONCLUSIONS: Lifetime psychotic experiences, particularly delusions, in the absence of mental disorders, are associated with later depressive disorders. Results persist in a dose‐response manner. Future research should determine whether transitory versus persistent psychotic experiences have a differential effect on later depression.
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spelling pubmed-99970722023-03-10 Association of Psychotic Experiences and Incident Depression in a Longitudinal Population‐Based Community Survey Rodriguez, Katrina M. Sharifi, Vandad Eaton, William W. Psychiatr Res Clin Pract Research Articles OBJECTIVE: The present study aims to determine if psychotic experiences in a general population sample are a risk factor for depressive disorders at a 15‐year follow‐up visit. METHOD: A longitudinal population cohort of adults over age 18 from East Baltimore were followed from 1981 to 1996 with 1409 participants included in analyses. Delusions and hallucinations and depressive disorders were assessed using DSM‐III criteria. Odds ratios were obtained using logistic regression with psychotic experiences modeled both dichotomously and as count variables as predictors of major and minor depressive disorders at wave three. Age, race, and sex were included as covariates in the model. RESULTS: Both delusions and hallucinations were associated with an increased odds of incident depressive disorders. Delusions, but not hallucinations, were associated with increased odds of major depressive disorder (adjusted odds ratio, 3.04 [95% CI = 1.29–7.13]) and both delusions and hallucinations were associated with increased odds of minor depressive disorder (adjusted odds ratios, 4.6 [95% CI = 2.11–10.04] and 3.93 [95% CI = 2.11–7.32]). There was a dose‐response relationship in number of psychotic experiences reported and odds of depressive disorders. CONCLUSIONS: Lifetime psychotic experiences, particularly delusions, in the absence of mental disorders, are associated with later depressive disorders. Results persist in a dose‐response manner. Future research should determine whether transitory versus persistent psychotic experiences have a differential effect on later depression. John Wiley and Sons Inc. 2023-01-30 /pmc/articles/PMC9997072/ /pubmed/36909140 http://dx.doi.org/10.1176/appi.prcp.20220021 Text en © 2023 The Authors. Psychiatric Research and Clinical Practice published by Wiley Periodicals LLC on behalf of American Psychiatric Association. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Rodriguez, Katrina M.
Sharifi, Vandad
Eaton, William W.
Association of Psychotic Experiences and Incident Depression in a Longitudinal Population‐Based Community Survey
title Association of Psychotic Experiences and Incident Depression in a Longitudinal Population‐Based Community Survey
title_full Association of Psychotic Experiences and Incident Depression in a Longitudinal Population‐Based Community Survey
title_fullStr Association of Psychotic Experiences and Incident Depression in a Longitudinal Population‐Based Community Survey
title_full_unstemmed Association of Psychotic Experiences and Incident Depression in a Longitudinal Population‐Based Community Survey
title_short Association of Psychotic Experiences and Incident Depression in a Longitudinal Population‐Based Community Survey
title_sort association of psychotic experiences and incident depression in a longitudinal population‐based community survey
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9997072/
https://www.ncbi.nlm.nih.gov/pubmed/36909140
http://dx.doi.org/10.1176/appi.prcp.20220021
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