Low predictive power of clinical features for relapse prediction after antidepressant discontinuation in a naturalistic setting
dc.contributor.author
Berwian, Isabel M.
dc.contributor.author
Wenzel, Julia G.
dc.contributor.author
Kuehn, Leonie
dc.contributor.author
Schnuerer, Inga
dc.contributor.author
Seifritz, Erich
dc.contributor.author
Stephan, Klaas
dc.contributor.author
Walter, Henrik
dc.contributor.author
Huys, Quentin J.M.
dc.date.accessioned
2022-07-27T13:59:29Z
dc.date.available
2022-07-09T11:23:35Z
dc.date.available
2022-07-27T13:59:29Z
dc.date.issued
2022-07-01
dc.identifier.issn
2045-2322
dc.identifier.other
10.1038/s41598-022-13893-9
en_US
dc.identifier.uri
http://hdl.handle.net/20.500.11850/557008
dc.identifier.doi
10.3929/ethz-b-000557008
dc.description.abstract
The risk of relapse after antidepressant medication (ADM) discontinuation is high. Predictors of relapse could guide clinical decision-making, but are yet to be established. We assessed demographic and clinical variables in a longitudinal observational study before antidepressant discontinuation. State-dependent variables were re-assessed either after discontinuation or before discontinuation after a waiting period. Relapse was assessed during 6 months after discontinuation. We applied logistic general linear models in combination with least absolute shrinkage and selection operator and elastic nets to avoid overfitting in order to identify predictors of relapse and estimated their generalisability using cross-validation. The final sample included 104 patients (age: 34.86 (11.1), 77% female) and 57 healthy controls (age: 34.12 (10.6), 70% female). 36% of the patients experienced a relapse. Treatment by a general practitioner increased the risk of relapse. Although within-sample statistical analyses suggested reasonable sensitivity and specificity, out-of-sample prediction of relapse was at chance level. Residual symptoms increased with discontinuation, but did not relate to relapse. Demographic and standard clinical variables appear to carry little predictive power and therefore are of limited use for patients and clinicians in guiding clinical decision-making.
en_US
dc.format
application/pdf
en_US
dc.language.iso
en
en_US
dc.publisher
Nature
en_US
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.subject
Psychology
en_US
dc.subject
Risk factors
en_US
dc.title
Low predictive power of clinical features for relapse prediction after antidepressant discontinuation in a naturalistic setting
en_US
dc.type
Journal Article
dc.rights.license
Creative Commons Attribution 4.0 International
ethz.journal.title
Scientific Reports
ethz.journal.volume
12
en_US
ethz.journal.issue
1
en_US
ethz.journal.abbreviated
Sci Rep
ethz.pages.start
11171
en_US
ethz.size
11 p.
en_US
ethz.version.deposit
publishedVersion
en_US
ethz.identifier.wos
ethz.identifier.scopus
ethz.publication.place
London
en_US
ethz.publication.status
published
en_US
ethz.leitzahl
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02140 - Dep. Inf.technologie und Elektrotechnik / Dep. of Inform.Technol. Electrical Eng.::02631 - Institut für Biomedizinische Technik / Institute for Biomedical Engineering::03955 - Stephan, Klaas E. / Stephan, Klaas E.
ethz.leitzahl.certified
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02140 - Dep. Inf.technologie und Elektrotechnik / Dep. of Inform.Technol. Electrical Eng.::02631 - Institut für Biomedizinische Technik / Institute for Biomedical Engineering::03955 - Stephan, Klaas E. / Stephan, Klaas E.
ethz.date.deposited
2022-07-09T11:24:20Z
ethz.source
WOS
ethz.eth
yes
en_US
ethz.availability
Open access
en_US
ethz.rosetta.installDate
2022-07-27T13:59:37Z
ethz.rosetta.lastUpdated
2023-02-07T04:53:09Z
ethz.rosetta.versionExported
true
ethz.COinS
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