Evidence map›Paper›PMID 41490977›Full record

ArticleTranslational psychiatry2026

Multimodal neuroimaging reveals brain neurochemical disturbances associated with superoxide dismutase in first-episode drug-naïve schizophrenia.

Zijia Zhu, Zhuo Wang, Xiuxia Yuan, Yawen Zou, Chenxiang Zheng, Yanqin Wen, Gangrui Hei, Xueqin Song, Yongyong Shi

Abstract read
In one paragraph

Article in Translational psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Zijia Zhu *Bio-X Institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Shanghai Jiao Tong University; Collaborative Innovation Centre for Brain Science, Shanghai Jiao Tong University, Shanghai, China.
Zhuo Wang *Bio-X Institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Shanghai Jiao Tong University; Collaborative Innovation Centre for Brain Science, Shanghai Jiao Tong University, Shanghai, China. zhuowang@sjtu.edu.cn.ORCID http://orcid.org/0000-0002-6382-1717
Xiuxia Yuan *Department of Psychiatry, the First Affiliated Hospital of Zhengzhou University; Henan International Joint Laboratory of Biological Psychiatry; Henan Psychiatric Transformation Research Key Laboratory/Zhengzhou University, Zhengzhou, China.
Yawen ZouBio-X Institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Shanghai Jiao Tong University; Collaborative Innovation Centre for Brain Science, Shanghai Jiao Tong University, Shanghai, China.
Chenxiang ZhengBio-X Institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Shanghai Jiao Tong University; Collaborative Innovation Centre for Brain Science, Shanghai Jiao Tong University, Shanghai, China.
Yanqin WenBio-X Institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Shanghai Jiao Tong University; Collaborative Innovation Centre for Brain Science, Shanghai Jiao Tong University, Shanghai, China.
Gangrui HeiDepartment of Psychiatry, the First Affiliated Hospital of Zhengzhou University; Henan International Joint Laboratory of Biological Psychiatry; Henan Psychiatric Transformation Research Key Laboratory/Zhengzhou University, Zhengzhou, China.
Xueqin SongDepartment of Psychiatry, the First Affiliated Hospital of Zhengzhou University; Henan International Joint Laboratory of Biological Psychiatry; Henan Psychiatric Transformation Research Key Laboratory/Zhengzhou University, Zhengzhou, China. fccsongxq@zzu.edu.cn.ORCID http://orcid.org/0000-0001-9830-7155
Yongyong ShiBio-X Institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Shanghai Jiao Tong University; Collaborative Innovation Centre for Brain Science, Shanghai Jiao Tong University, Shanghai, China. shiyongyong@gmail.com.ORCID http://orcid.org/0000-0003-1710-1505

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Reduced antioxidant defense observed in first-episode drug-naïve schizophrenia (SCZ) may contribute to impaired cognition of SCZ. However, the underlying relationships among antioxidant stress-neuroimaging-cognition pathway and neurotransmitter dysfunction remain unclear. In this study, 75 patients with first-episode drug-naïve SCZ and 85 age and sex matched healthy controls underwent clinical evaluation and brain MRI. Two brain imaging measurements, including gray matter volume (GMV) from structural MRI (sMRI) and fractional amplitude of low frequency fluctuations (fALFF) from resting-state functional MRI, were jointly analyzed with a data-driven multivariate fusion method. Serum superoxide dismutase (SOD) levels was used as a reference to guide fusion of two MRI features. To investigate specific neurotransmitter system alterations associated with SOD-related SCZ patients, we used the JuSpace toolbox for cross-modal correlations between two MRI-based modalities with nuclear imaging derived estimates. Two multimodal components (IC5 and IC7) show significant group difference in loadings. We found significant associations of SOD with both GMV and fALFF within the frontoparietal and default mode networks (DMN). Furthermore, the covariant structural-functional components linked with reduced SOD levels were associated with deficits in cognitive function in speed of processing and visual learning. Moreover, the spatial correlation analysis identified associations of altered neuroimaging fusion biomarkers with disrupted excitatory-inhibitory neurotransmitter receptor distribution. This study unveils the complex alterations in SCZ across structural, functional, and neurochemical dimensions through multimodal analysis, highlighting the association between SOD-induced oxidative stress and imbalances in the excitatory/inhibitory ratio in the core brain regions of the DMN. Antioxidant therapy may have the potential to alleviate cognition deficit in SCZ patients in the future.

Indexed as

BrainSchizophreniaSuperoxide DismutaseAdultCase-Control StudiesFemaleGray MatterHumansMagnetic Resonance ImagingMaleMultimodal ImagingNeuroimagingYoung AdultSuperoxide Dismutase

Identifiers

PMID41490977
PMCPMC12804751

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.