Evidence map›Paper›PMID 36975001›Full record

ReviewThe international journal of neuropsychopharmacology2023

Redox and Immune Signaling in Schizophrenia: New Therapeutic Potential.

Daniella Dwir, Ines Khadimallah, Lijing Xin, Meredith Rahman, Fei Du, Dost Öngür, Kim Q Do

Abstract readReview
In one paragraph

Review in The international journal of neuropsychopharmacology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Trial
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  4. DifferentialScience advances · 2026
    Article
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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

7 authors.

Daniella DwirCenter for Psychiatric Neuroscience, Department of Psychiatry, Lausanne University Hospital and University of Lausanne, Route de Cery, 1008 Prilly-Lausanne, Switzerland.ORCID 0000-0003-4931-9007
Ines KhadimallahCenter for Psychiatric Neuroscience, Department of Psychiatry, Lausanne University Hospital and University of Lausanne, Route de Cery, 1008 Prilly-Lausanne, Switzerland.
Lijing XinCenter for Biomedical Imaging (CIBM), Ecole Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.
Meredith RahmanVirginia Tech Carilion School of Medicine, Roanoke, Virginia, USA.
Fei DuPsychotic Disorders Division, McLean Hospital, Harvard Medical School, Belmont, Massachusetts, USA.
Dost ÖngürPsychotic Disorders Division, McLean Hospital, Harvard Medical School, Belmont, Massachusetts, USA.
Kim Q DoCenter for Psychiatric Neuroscience, Department of Psychiatry, Lausanne University Hospital and University of Lausanne, Route de Cery, 1008 Prilly-Lausanne, Switzerland.ORCID 0000-0003-1968-1646

Funding

Randomized controlled trial of enhanced coordinated specialty care (CSC 2.0)P50MH115846 · NIMH · MCLEAN HOSPITAL · PI Dost Ongur · 2019 to 2026
$16.9M
Molecular Mechanisms and Biomarkers for Disease Progression from Prodrome to Early PsychosisR01MH114982 · NIMH · MCLEAN HOSPITAL · PI DU, FEI, ONGUR, DOST · 2019 to 2023
$2.4M
NIMH NIH HHS P50 MH115846NIMH NIH HHS R01 MH114982Swiss National Science Foundation 51AU40_185897
6 · The paper itself

Abstract

Redox biology and immune signaling play major roles in the body, including in brain function. A rapidly growing literature also suggests that redox and immune abnormalities are implicated in neuropsychiatric conditions such as schizophrenia (SZ), bipolar disorder, autism, and epilepsy. In this article we review this literature, its implications for the pathophysiology of SZ, and the potential for development of novel treatment interventions targeting redox and immune signaling. Redox biology and immune signaling in the brain are complex and not fully understood; in addition, there are discrepancies in the literature, especially in patient-oriented studies. Nevertheless, it is clear that abnormalities arise in SZ from an interaction between genetic and environmental factors during sensitive periods of brain development, and these abnormalities disrupt local circuits and long-range connectivity. Interventions that correct these abnormalities may be effective in normalizing brain function in psychotic disorders, especially in early phases of illness.

Indexed as

Bipolar DisorderPsychotic DisordersSchizophreniaHumansOxidation-ReductionOxidative StressglutathioneNAD/NADHneuro-inflammationOxidative stressparvalbumin neuronsschizophrenia

Identifiers

PMID36975001
PMCPMC10229853

What OpenQuestion holds

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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.