Evidence map›Paper›PMID 40583536›Full record

ArticleSchizophrenia bulletin2026

A Longitudinal Assessment of Anterior Cingulate Cortex Gamma-aminobutyric Acid in Antipsychotic Medication-naïve First Episode Psychosis Patients.

Genelle D Samson, Jose O Maximo, Eric A Nelson, Nina V Kraguljac, William P Armstrong, Branden Benningfield, Seyedeh Nasim Adnani, Adil Bashir, Adrienne C Lahti

Abstract read
In one paragraph

Article in Schizophrenia bulletin, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

9 authors.

Genelle D SamsonDepartment of Psychology, University of Alabama at Birmingham, Birmingham, United States.ORCID 0000-0001-5672-847X
Jose O MaximoDepartment of Psychiatry and Behavioral Neurobiology, University of Alabama at Birmingham, Birmingham, United States.
Eric A NelsonDepartment of Psychiatry and Behavioral Neurobiology, University of Alabama at Birmingham, Birmingham, United States.
Nina V KraguljacDepartment of Psychiatry and Behavioral Health, Ohio State University, Columbus, United States.
William P ArmstrongDepartment of Psychiatry and Behavioral Neurobiology, University of Alabama at Birmingham, Birmingham, United States.
Branden BenningfieldDepartment of Psychiatry and Behavioral Neurobiology, University of Alabama at Birmingham, Birmingham, United States.
Seyedeh Nasim AdnaniDepartment of Electrical & Computer Engineering, Auburn University, Auburn, United States.
Adil BashirDepartment of Electrical & Computer Engineering, Auburn University, Auburn, United States.
Adrienne C LahtiDepartment of Psychiatry and Behavioral Neurobiology, University of Alabama at Birmingham, Birmingham, United States.

Funding

Trajectories of treatment response as window into the heterogeneity of psychosis: a longitudinal multimodal imaging study in medication-naieve first episode psychosis patientsR01MH113800 · NIMH · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI LAHTI, ADRIENNE C · 2018 to 2022
$3.9M
Glutamate, brain connectivity and duration of untreated psychosisR01MH102951 · NIMH · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI LAHTI, ADRIENNE C · 2014 to 2018
$2.9M
NIMH NIH HHS R01 MH102951NIMH NIH HHS R01MH102951NIMH NIH HHS R01 MH113800NIMH NIH HHS R01MH113800
6 · The paper itself

Abstract

background and hypothesisConverging evidence from animal and human studies has implicated gamma-aminobutyric acid (GABA)-ergic dysfunction in the pathophysiology of psychosis spectrum disorders. However, little is known about GABA's role in the early illness stages. Based on prior research, we hypothesized that GABA levels would already be altered in first episode psychosis patients (FEP), and that they would be associated with patients' cognitive function and response to treatment. STUDY

designWe used magnetic resonance spectroscopy with a MEGA-PRESS sequence to quantify GABA in the dorsal anterior cingulate cortex (ACC) at baseline and over the course of antipsychotic treatment with risperidone. We compared GABA levels between 79 medication-naïve FEP and 113 healthy controls (HC) longitudinally over a period of 16 weeks and examined their relationships to cognition and treatment response. STUDY

resultsWe found significantly lower GABA levels in FEP compared to HC at all 3 time points (baseline, 6 weeks, 16 weeks), but did not observe a significant main effect of time or an interaction of group by time. We found no significant correlations between GABA and cognitive scores. Baseline GABA levels of patients considered treatment nonresponders significantly differed from HC, whereas responders did not.

conclusionsOur findings suggest that GABA dysfunction in the ACC may be an important feature of the core pathophysiology of psychosis. This dysfunction does not appear to be attenuated by conventional antipsychotic treatment, though baseline levels may be indicative of clinical prognosis in FEP.

Indexed as

Antipsychotic AgentsCognitive Dysfunctiongamma-Aminobutyric AcidGyrus CinguliPsychotic DisordersRisperidoneSchizophreniaAdolescentAdultFemaleHumansLongitudinal StudiesMagnetic Resonance SpectroscopyMaleYoung AdultAntipsychotic Agentsgamma-Aminobutyric AcidRisperidonecognitionGABAmagnetic resonance spectroscopyMEGA-PRESSschizophreniatreatment response

Identifiers

PMID40583536
PMCPMC12996905

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.