Evidence map›Paper›PMID 38553640›Full record

Trial reportEuropean archives of psychiatry and clinical neuroscience2024

Comparing the latent state-trait structure of the PANSS in cariprazine-medicated and placebo-controlled patients with acute schizophrenia.

Jana S Krückl, Károly Acsai, Zsófia B Dombi, Julian Moeller, Roselind Lieb, Undine E Lang, Ágota Barabássy, Christian G Huber

Abstract readClinical Trial, Phase IIRandomized Controlled TrialClinical Trial, Phase III
In one paragraph

Trial report in European archives of psychiatry and clinical neuroscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Jana S KrücklPsychiatric University Clinic (UPK Basel), University of Basel, Wilhelm Klein - Strasse 27, 4002, Basel, Switzerland. jana.krueckl@unibas.ch.ORCID http://orcid.org/0000-0002-0647-5782
Károly AcsaiGlobal Medical Division, Gedeon Richter Plc, Budapest, Hungary.
Zsófia B DombiGlobal Medical Division, Gedeon Richter Plc, Budapest, Hungary.ORCID http://orcid.org/0000-0002-0390-4852
Julian MoellerPsychiatric University Clinic (UPK Basel), University of Basel, Wilhelm Klein - Strasse 27, 4002, Basel, Switzerland.ORCID http://orcid.org/0000-0002-7823-3651
Roselind LiebDepartment of Psychology, Division of Clinical Psychology and Epidemiology, University of Basel, Basel, Switzerland.ORCID http://orcid.org/0000-0002-2039-2262
Undine E LangPsychiatric University Clinic (UPK Basel), University of Basel, Wilhelm Klein - Strasse 27, 4002, Basel, Switzerland.ORCID http://orcid.org/0000-0002-3585-6533
Ágota BarabássyGlobal Medical Division, Gedeon Richter Plc, Budapest, Hungary.
Christian G HuberPsychiatric University Clinic (UPK Basel), University of Basel, Wilhelm Klein - Strasse 27, 4002, Basel, Switzerland.ORCID http://orcid.org/0000-0002-2246-9008

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

After over a hundred years of research, the question whether the symptoms of schizophrenia are rather trait-like (being a relatively stable quality of individuals) or state-like (being substance to change) is still unanswered. To assess the trait and the state component in patients with acute schizophrenia, one group receiving antipsychotic treatment, the other not. Data from four phase II/III, 6-week, randomized, double-blind, placebo-controlled trials of similar design that included patients with acute exacerbation of schizophrenia were pooled. In every trial, one treatment group received a third-generation antipsychotic, cariprazine, and the other group placebo. To assess symptoms of schizophrenia, the Positive and Negative Symptom Scale (PANSS) was applied. Further analyses were conducted using the five subscales as proposed by Wallwork and colleagues. A latent state-trait (LST) model was developed to estimate the trait and state components of the total variance of the observed scores. All symptom dimensions behaved more in a trait-like manner. The proportions of all sources of variability changed over the course of the observational period, with a bent around weeks 3 and 4. Visually inspected, no major differences were found between the two treatment groups regarding the LST structure of symptom dimensions. This high proportion of inter-individual stability may represent an inherent part of symptomatology that behaves independently from treatment status.

Indexed as

Antipsychotic AgentsPiperazinesSchizophreniaAcute DiseaseAdultDouble-Blind MethodFemaleHumansMaleMiddle AgedPsychiatric Status Rating ScalesYoung AdultAntipsychotic AgentscariprazinePiperazinesCariprazineFive-factor modelLatent state–trait modelPANSSSchizophrenia

Identifiers

PMID38553640
PMCPMC11362189

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.