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dc.contributor.authorDrosos, Petros
dc.contributor.authorJohnsen, Erik
dc.contributor.authorBartz-Johannessen, Christoffer
dc.contributor.authorLarsen, Tor Ketil
dc.contributor.authorReitan, Solveig Klæbo
dc.contributor.authorRettenbacher, Maria
dc.contributor.authorKroken, Rune Andreas
dc.date.accessioned2024-05-23T11:31:19Z
dc.date.available2024-05-23T11:31:19Z
dc.date.created2023-02-17T14:45:50Z
dc.date.issued2022
dc.identifier.citationWorld Journal of Psychiatry (WJP). 2022, 19 (12), 521-532.en_US
dc.identifier.issn2220-3206
dc.identifier.urihttps://hdl.handle.net/11250/3131230
dc.description.abstractBACKGROUND: Antipsychotic drugs remain the mainstay of schizophrenia treatment; however, their effectiveness has been questioned, and it is not possible to predict the response to a specific antipsychotic drug in an individual patient. Thus, it is important to compare the effectiveness of the various antipsychotics and search for possible response predictors. AIM: To investigate the effectiveness of antipsychotic drugs, we examined response trajectories and predictors for belonging to different trajectory groups. METHODS: The Bergen-Stavanger-Innsbruck-Trondheim (BeSt InTro) trial compared the effectiveness of three atypical antipsychotics-amisulpride, aripiprazole, and olanzapine-in a prospective, semirandomized, rater-blind, head-to-head design. Adult participants with a schizophrenia spectrum disorder diagnosis, according to international classification of diseases, Tenth Revision (ICD-10) F20–29, were included. Participants were followed for a period of 12 mo, with assessments at baseline; after one, three and six weeks; and after three, six, nine and 12 mo. A latent class mixed model was fitted to our data. The three-trajectory model based on the Positive and Negative Syndrome Scale (PANSS) total score reduction was found to have adequate fit, and the study drugs, as well as various demographic and clinical parameters, were tested as predictors for belonging to the different trajectory groups. RESULTS: Overall, 144 participants were included, and 41% completed the 12-mo study period. The largest trajectory group, consisting of 74% of participants, showed a PANSS total score reduction of 59% from baseline to 12 mo (Good response group). A trajectory group comprising 13% of participants had their PANSS total score reduced by 82.5% at 12 mo (Strong response group), while the last response trajectory group comprising 13% of the participants had a PANSS total score reduction of 13.6% (Slight response group). The largest part of the total reduction for the Good and Strong response groups occurred at six weeks of treatment, amounting to 45% and 48% reductions from baseline, respectively. The use of amisulpride predicted belonging to the Strong response group, while unemployment, depression, and negative psychotic symptoms at baseline increased the chance of belonging to the Slight response group, indicating a poor response to antipsychotic drug treatment. CONCLUSION: Most of the participants (87%) had a good outcome after one year. Amisulpride users, more often than aripiprazole and olanzapine users, belonged to the response trajectory group with a strong response.en_US
dc.language.isoengen_US
dc.publisherBaishideng Publishing Group (BPG)en_US
dc.rightsNavngivelse-Ikkekommersiell 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/deed.no*
dc.titleTrajectories of response in schizophrenia-spectrum disorders: A one-year prospective cohort study of antipsychotic effectivenessen_US
dc.title.alternativeTrajectories of response in schizophrenia-spectrum disorders: A one-year prospective cohort study of antipsychotic effectivenessen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber521-532en_US
dc.source.volume12en_US
dc.source.journalWorld Journal of Psychiatry (WJP)en_US
dc.source.issue3en_US
dc.identifier.doi10.5498/wjp.v12.i3.521
dc.identifier.cristin2127058
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode0


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Navngivelse-Ikkekommersiell 4.0 Internasjonal
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