Evidence map›Paper›PMID 42183481›Full record

ArticleSchizophrenia bulletin open2026

A Systematic Review of the Magnetic Resonance Imaging Literature Investigating the Deficit Syndrome in Schizophrenia.

Matheus Teles G de Araujo, Jordan Sloan Larson, James Edward Bryant, Nina Vanessa Kraguljac

Abstract read
In one paragraph

Article in Schizophrenia bulletin open, 2026. 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

4 authors.

Matheus Teles G de AraujoDepartment of Psychology, University of Alabama at Birmingham, Birmingham, AL 35233,  United States.ORCID https://orcid.org/0000-0001-7622-0606
Jordan Sloan LarsonDepartment of Psychiatry and Behavioral Health, The Ohio State University, Columbus, OH 43210,  United States.
James Edward BryantDepartment of Psychiatry and Behavioral Health, The Ohio State University, Columbus, OH 43210,  United States.
Nina Vanessa KraguljacDepartment of Psychiatry and Behavioral Health, The Ohio State University, Columbus, OH 43210,  United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Hypotheses: Heterogeneity in schizophrenia is significant but remains poorly understood. Treatment strategies have not evolved beyond one-size-fits-all approaches, often delaying the discovery of effective treatments and better outcomes. The deficit syndrome was proposed as a more homogenous subtype of the illness that is characterized by primary and enduring negative symptoms. We reviewed Magnetic Resonance Imaging (MRI) studies examining brain structure, function, and neurometabolism in deficit syndrome with the goal of identifying unique brain signatures for this subtype of schizophrenia. Study Design: Systematic Review of MRI studies published between 1999 and 2024 on the deficit syndrome. Study Results: Potentially unique features of the deficit syndrome include nucleus accumbens and cerebellar gray matter volume deficits, reduced uncinate fasciculus fractional anisotropy, fronto-parietal and default mode network dysconnectivity, altered global efficiency, and shortest path-length in brain network organization. Further, abnormalities in cerebellar culmen volume and cerebellar spontaneous activation may differ only in degree between patient groups. Many findings warrant replication and must be interpreted with caution. Conclusions: The deficit syndrome is hypothesized to be different from other forms of schizophrenia and more homogenous in its pathophysiology. Magnetic Resonance Imaging studies examining neurobiological group differences show conflicting results; some report that the deficit syndrome may be distinct, while others find that brain pathology is more severe or shared across subtypes. No MRI studies have directly tested if inter-individual heterogeneity in brain pathology is lower in the deficit syndrome, which would be necessary to determine if this clinically more homogenous subtype is also neurobiologically more homogenous.

Indexed as

deficit syndromeimagingschizophrenia

Identifiers

PMID42183481
PMCPMC13191110

What OpenQuestion holds

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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.