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Epidemiology of psychotic depression – systematic review and meta-analysis

Published online by Cambridge University Press:  12 September 2017

E. Jääskeläinen*
Affiliation:
Center for Life Course Health Research, University of Oulu, Finland Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Finland Department of Psychiatry, Oulu University Hospital, Finland
T. Juola
Affiliation:
Center for Life Course Health Research, University of Oulu, Finland
H. Korpela
Affiliation:
Center for Life Course Health Research, University of Oulu, Finland Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Finland
H. Lehtiniemi
Affiliation:
Center for Life Course Health Research, University of Oulu, Finland
M. Nietola
Affiliation:
Psychiatric Department, University of Turku and Turku University Hospital, Finland
J. Korkeila
Affiliation:
Psychiatric Department, University of Turku and Satakunta Hospital District, Finland
J. Miettunen
Affiliation:
Center for Life Course Health Research, University of Oulu, Finland Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Finland
*
*Address for correspondence: E. Jääskeläinen, Center for Life Course Health Research, P.O. Box 5000, University of Oulu, Oulu 90014, Finland. (Email: erika.jaaskelainen@oulu.fi)

Abstract

Large amount of data have been published on non-psychotic depression (NPD), schizophrenia (SZ), and bipolar disorder, while psychotic depression (PD) as an own entity has received much smaller attention. We performed a systematic review and meta-analyses on epidemiology, especially incidence and prevalence, risk factors, and outcomes of PD. A systematic search to identify potentially relevant studies was conducted using four electronic databases and a manual search. The search identified 1764 unique potentially relevant articles, the final study included 99 articles. We found that the lifetime prevalence of PD varies between 0.35% and 1%, with higher rates in older age. Onset age of PD was earlier than that of NPD in younger samples, but later in older samples. There were no differences in gender distribution in PD v. NPD, but higher proportion of females was found in PD than in SZ or in psychotic bipolar disorder (PBD). Risk factors have rarely been studied, the main finding being that family history of psychosis and bipolar disorder increases the risk of PD. Outcomes of PD were mostly worse when compared with NPD, but better compared with SZ and schizoaffective disorder. The outcome compared with PBD was relatively similar, and somewhat varied depending on the measure of the outcome. Based on this review, the amount of research on PD is far from that of NPD, SZ, and bipolar disorder. Based on our findings, PD seems distinguishable from related disorders and needs more scientific attention.

Type
Review Article
Copyright
Copyright © Cambridge University Press 2017 

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Footnotes

These authors contributed equally to this work.

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