Evidence map›Paper›PMID 32924060›Full record

ArticleCerebral cortex (New York, N.Y. : 1991)2021

Lipid Pathology of the Corpus Callosum in Schizophrenia and the Potential Role of Abnormal Gene Regulatory Networks with Reduced Microglial Marker Expression.

Chie Shimamoto-Mitsuyama, Akihiro Nakaya, Kayoko Esaki, Shabeesh Balan, Yoshimi Iwayama, Tetsuo Ohnishi, Motoko Maekawa, Tomoko Toyota, Brian Dean, Takeo Yoshikawa

Open access · hybridAbstract read
In one paragraph

Article in Cerebral cortex (New York, N.Y. : 1991), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 4 pooled it
2.1field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 4 syntheses or guidelines pooled it, 43 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. The role ofEpigenetics · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. White matter lipidome alterations in the schizophrenia brain.Schizophrenia (Heidelberg, Germany) · 2024
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Associations between forensic loci and expression levels of neighboring genes may compromise medical privacy.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  17. Review
  18. 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

10 authors at 2 institutions in 2 countries.

Chie Shimamoto-MitsuyamaLaboratory of Molecular Psychiatry, RIKEN Center for Brain Science, Wako, Saitama, Japan.
Akihiro NakayaLaboratory of Molecular Psychiatry, RIKEN Center for Brain Science, Wako, Saitama, Japan.
Kayoko EsakiLaboratory of Molecular Psychiatry, RIKEN Center for Brain Science, Wako, Saitama, Japan.
Shabeesh BalanLaboratory of Molecular Psychiatry, RIKEN Center for Brain Science, Wako, Saitama, Japan.
Yoshimi IwayamaLaboratory of Molecular Psychiatry, RIKEN Center for Brain Science, Wako, Saitama, Japan.
Tetsuo OhnishiLaboratory of Molecular Psychiatry, RIKEN Center for Brain Science, Wako, Saitama, Japan.
Motoko MaekawaLaboratory of Molecular Psychiatry, RIKEN Center for Brain Science, Wako, Saitama, Japan.
Tomoko ToyotaLaboratory of Molecular Psychiatry, RIKEN Center for Brain Science, Wako, Saitama, Japan.
Brian DeanThe Florey Institute of Neuroscience and Mental Health, Howard Florey Laboratories, The University of Melbourne, Parkville, Victoria, Australia.
Takeo YoshikawaLaboratory of Molecular Psychiatry, RIKEN Center for Brain Science, Wako, Saitama, Japan.
RIKEN Center for Brain Science · JPThe University of Melbourne · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Structural changes in the corpus callosum have been reported in schizophrenia; however, the underlying molecular mechanism remains unclear. As the corpus callosum is high in lipid content, we analyzed the lipid contents of the corpora callosa from 15 patients with schizophrenia and 15 age- and sex-matched controls using liquid chromatography coupled to tandem mass spectrometry and identified lipid combinations associated with schizophrenia. Real-time quantitative polymerase chain reaction analyses using extended samples (schizophrenia, n = 95; control, n = 91) showed low expression levels of lipid metabolism-related genes and their potential upstream transcription factors in schizophrenia. Subsequent pathway analysis identified a gene regulatory network where nuclear factor of activated T cells 2 (NFATC2) is placed most upstream. We also observed low gene expression levels of microglial markers, inflammatory cytokines, and colony-stimulating factor 1 receptor (CSF1R), which is known to regulate the density of microglia, in the corpus callosum in schizophrenia. The interactions between CSF1R and several genes in the presently identified gene network originating from NFATC2 have been reported. Collectively, this study provides evidence regarding lipid abnormalities in the corpora callosa of patients with schizophrenia and proposes the potential role of impaired "NFATC2-relevant gene network-microglial axis" as its underlying mechanism.

Indexed as

LipidsAdultBiomarkersChromatography, LiquidCorpus CallosumCytokinesFemaleGene Regulatory NetworksHumansMaleMicrogliaMiddle AgedSchizophreniaBiomarkersCytokinesLipidsarachidonic acidgene expressionliquid chromatography coupled to tandem mass spectrometry (LC–MS/MS)microgliapostmortem brain

Identifiers

PMID32924060
PMCPMC7727339
OpenAlexW3084656369

What OpenQuestion holds

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LicenceCC BY-NC
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.