Evidence map›Paper›PMID 40817104›Full record

ArticleSchizophrenia (Heidelberg, Germany)2025

Longitudinal changes in striatocortical connectivity in first-episode psychosis associated with the emergence of treatment resistance.

Angeles Tepper, Javiera Vásquez, Camila Díaz Dellarossa, Juan Pablo Ramirez-Mahaluf, Juan Aguirre, Daniella Barbagelata, David Aceituno, Juan Undurraga, Ruben Nachar, Cristian Mena and 4 more

Abstract read
In one paragraph

Article in Schizophrenia (Heidelberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

14 authors.

Angeles TepperDepartment of Psychiatry, Pontificia Universidad Católica de Chile, Santiago, Chile.ORCID http://orcid.org/0000-0001-9506-1305
Javiera VásquezDepartment of Psychiatry, Pontificia Universidad Católica de Chile, Santiago, Chile.
Camila Díaz DellarossaPharmacovigilance Program, Instituto Psiquiátrico José Horwitz Barak, Santiago, Chile.
Juan Pablo Ramirez-MahalufDepartment of Psychiatry, Pontificia Universidad Católica de Chile, Santiago, Chile.
Juan AguirreDepartment of Psychiatry, Pontificia Universidad Católica de Chile, Santiago, Chile.
Daniella BarbagelataDepartment of Psychiatry, Pontificia Universidad Católica de Chile, Santiago, Chile.
David AceitunoDepartment of Psychiatry, Pontificia Universidad Católica de Chile, Santiago, Chile.
Juan UndurragaUniversidad del Desarrollo-Clínica Alemana, Santiago, Chile.ORCID http://orcid.org/0000-0001-6958-2369
Ruben NacharPrograma de Intervención Temprana (PROITP), Instituto Psiquiátrico José Horwitz Barak, Santiago, Chile.
Cristian MenaPrograma de Intervención Temprana (PROITP), Instituto Psiquiátrico José Horwitz Barak, Santiago, Chile.ORCID http://orcid.org/0000-0003-1906-1156
Robert A McCutcheonDepartment of Psychiatry, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0003-1102-2566
Philip McGuireDepartment of Psychiatry, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0003-4381-0532
Alfonso Gonzalez-ValderramaPrograma de Intervención Temprana (PROITP), Instituto Psiquiátrico José Horwitz Barak, Santiago, Chile.
Nicolas A CrossleyDepartment of Psychiatry, Pontificia Universidad Católica de Chile, Santiago, Chile. ncrossley@uc.cl.ORCID http://orcid.org/0000-0002-3060-656X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Treatment resistance affects up to one in four individuals with psychosis in the first few years of illness. However, there is limited information about the brain changes associated with treatment resistance, restricting our ability to develop effective prognostic biomarkers or new treatments. Using resting-state functional MRI, we examined striatocortical connectivity in 87 patients who presented a non-affective first-episode of psychosis and 118 healthy controls, with follow-up imaging on more than half of the participants in the next 6 years, totaling 361 images. Crucially, we identified 30 patients who presented treatment-resistant psychosis in this follow-up period. Thus, we examined baseline (at first episode) and longitudinal striatocortical differences within psychosis subgroups (treatment-responsive and treatment-resistant psychosis), and between patients subgroups and healthy controls. Compared to healthy controls, participants with treatment-responsive psychosis presented baseline differences in functional connectivity of ventral striatal systems, without changes over time; whereas patients with treatment-resistant psychosis showed both baseline and longitudinal differences in ventral striatal systems, compared to healthy controls. Treatment-responsive and treatment-resistant psychosis groups differed in longitudinal changes in connectivity between ventral striatal and temporal cortical regions. This is one of the circuits which has been previously related to symptom improvements in patients with first-episode of psychosis. No baseline differences were observed between the two psychosis groups. Overall, treatment-resistant psychosis is characterized by longitudinal changes in striatal systems in early psychosis, which might be used as the basis of future prognostic biomarkers.

Identifiers

PMID40817104
PMCPMC12356903

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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.