Evidence map›Paper›PMID 38007605›Full record

ArticleSchizophrenia bulletin2024

Disease Progression Patterns of Brain Morphology in Schizophrenia: More Progressed Stages in Treatment Resistance.

Daichi Sone, Alexandra Young, Shunichiro Shinagawa, Sakiko Tsugawa, Yusuke Iwata, Ryosuke Tarumi, Kamiyu Ogyu, Shiori Honda, Ryo Ochi, Karin Matsushita and 19 more

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in Schizophrenia bulletin, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.1field-weighted citation impact, top 5% of its field
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

11 citing papers in PubMed, 18 citations in OpenAlex.

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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

29 authors at 4 institutions in 3 countries.

Daichi SoneDepartment of Psychiatry, Jikei University School of Medicine, Tokyo, Japan.ORCID 0000-0001-9617-706X
Alexandra YoungDepartment of Neuroimaging, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.ORCID 0000-0002-7772-781X
Shunichiro ShinagawaDepartment of Psychiatry, Jikei University School of Medicine, Tokyo, Japan.
Sakiko TsugawaDepartment of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
Yusuke IwataDepartment of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
Ryosuke TarumiDepartment of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
Kamiyu OgyuDepartment of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
Shiori HondaDepartment of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
Ryo OchiDepartment of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
Karin MatsushitaDepartment of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
Fumihiko UenoDepartment of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
Nobuaki HondoDepartment of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
Akihiro KorekiDepartment of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.ORCID 0000-0003-0132-9724
Edgardo Torres-CarmonaDepartment of Psychiatry, University of Toronto, Toronto, Canada.
Wanna MarDepartment of Psychiatry, University of Toronto, Toronto, Canada.
Nathan ChanDepartment of Psychiatry, University of Toronto, Toronto, Canada.
Teruki KoizumiDepartment of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
Hideo KatoDepartment of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
Keisuke KusudoDepartment of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
Vincenzo de LucaDepartment of Psychiatry, University of Toronto, Toronto, Canada.
Philip GerretsenDepartment of Psychiatry, University of Toronto, Toronto, Canada.
Gary RemingtonDepartment of Psychiatry, University of Toronto, Toronto, Canada.ORCID 0000-0001-9433-9416
Mitsumoto OnayaDepartment of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
Yoshihiro NodaDepartment of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
Hiroyuki UchidaDepartment of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.ORCID 0000-0002-0628-7036
Masaru MimuraDepartment of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
Masahiro ShigetaDepartment of Psychiatry, Jikei University School of Medicine, Tokyo, Japan.
Ariel Graff-GuerreroDepartment of Psychiatry, University of Toronto, Toronto, Canada.
Shinichiro NakajimaDepartment of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
Keio University · JPUniversity of Toronto · CAJikei University School of Medicine · JPKing's College London · GB

Funding

CIHR MOP-142493
6 · The paper itself

Abstract

background and hypothesisGiven the heterogeneity and possible disease progression in schizophrenia, identifying the neurobiological subtypes and progression patterns in each patient may lead to novel biomarkers. Here, we adopted data-driven machine-learning techniques to identify the progression patterns of brain morphological changes in schizophrenia and investigate the association with treatment resistance. STUDY

designIn this cross-sectional multicenter study, we included 177 patients with schizophrenia, characterized by treatment response or resistance, with 3D T1-weighted magnetic resonance imaging. Cortical thickness and subcortical volumes calculated by FreeSurfer were converted into z scores using 73 healthy controls data. The Subtype and Stage Inference (SuStaIn) algorithm was used for unsupervised machine-learning analysis. STUDY

resultsSuStaIn identified 3 different subtypes: (1) subcortical volume reduction (SC) type (73 patients), in which volume reduction of subcortical structures occurs first and moderate cortical thinning follows, (2) globus pallidus hypertrophy and cortical thinning (GP-CX) type (42 patients), in which globus pallidus hypertrophy initially occurs followed by progressive cortical thinning, and (3) cortical thinning (pure CX) type (39 patients), in which thinning of the insular and lateral temporal lobe cortices primarily happens. The remaining 23 patients were assigned to baseline stage of progression (no change). SuStaIn also found 84 stages of progression, and treatment-resistant schizophrenia showed significantly more progressed stages than treatment-responsive cases (P = .001). The GP-CX type presented earlier stages than the pure CX type (P = .009).

conclusionsThe brain morphological progressions in schizophrenia can be classified into 3 subtypes, and treatment resistance was associated with more progressed stages, which may suggest a novel biomarker.

Indexed as

SchizophreniaBrainCerebral CortexCerebral Cortical ThinningCross-Sectional StudiesDisease ProgressionHumansHypertrophyMagnetic Resonance ImagingTemporal Lobebrain morphologydisease progressionmachine learningmagnetic resonance imagingschizophrenia

Identifiers

PMID38007605
PMCPMC10919766
OpenAlexW4389005275

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.