Evidence map›Paper›PMID 42557393›Full record

ArticleMolecular psychiatry2026

Neuroinflammation as molecular landscape of post-operative delirium revealed by live human brain multi-omics profiling.

Takaya Ishii, Tao Wang, Kazuki Shibata, Shota Nishitani, Takehiko Yamanashi, Nadia E Wahba, Tomoteru Seki, Kaitlyn J Thompson, Kyosuke Yamanishi, Tsuyoshi Nishiguchi and 14 more

Abstract read
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In one paragraph

Article in Molecular psychiatry, 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

24 authors.

Takaya IshiiDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Palo Alto, CA, USA.ORCID http://orcid.org/0000-0001-6026-8664
Tao WangDepartment of Genetics, Stanford University School of Medicine, Stanford, CA, USA.
Kazuki ShibataDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Palo Alto, CA, USA.
Shota NishitaniDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Palo Alto, CA, USA.
Takehiko YamanashiFaculty of Medicine, Department of Neuropsychiatry, Tottori University, Yonago, Tottori, Japan.ORCID http://orcid.org/0000-0002-3881-8997
Nadia E WahbaDepartment of Psychiatry, University of Iowa Carver College of Medicine, Iowa City, IA, USA.
Tomoteru SekiDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Palo Alto, CA, USA.ORCID http://orcid.org/0000-0003-2593-7118
Kaitlyn J ThompsonDepartment of Psychiatry, University of Iowa Carver College of Medicine, Iowa City, IA, USA.
Kyosuke YamanishiDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Palo Alto, CA, USA.
Tsuyoshi NishiguchiDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Palo Alto, CA, USA.
Akiyoshi ShimuraDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Palo Alto, CA, USA.ORCID http://orcid.org/0000-0003-0806-4423
Bun AoyamaDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Palo Alto, CA, USA.
Nipun GorantlaDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Palo Alto, CA, USA.
Nathan J PhuongDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Palo Alto, CA, USA.ORCID http://orcid.org/0009-0003-8374-782X
Hieu D NguyenDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Palo Alto, CA, USA.
Therese A SantiagoDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Palo Alto, CA, USA.
Yoshitaka NishizawaDepartment of Psychiatry, Osaka Medical and Pharmaceutical University School of Medicine, Osaka, Japan.
Takaaki NagaoDepartment of Neurosurgery (Sakura), Toho University School of Medicine Faculty of Medicine, Sakura, Chiba, Japan.
Mathew A HowardDepartment of Neurosurgery, University of Iowa Carver College of Medicine, Iowa City, IA, USA.
Hiroto KawasakiDepartment of Neurosurgery, University of Iowa Carver College of Medicine, Iowa City, IA, USA.
Kyosuke HinoRegenerative & Cellular Medicine Kobe Center, Sumitomo Pharma Co., Ltd., Osaka, Japan.ORCID http://orcid.org/0009-0000-4681-9730
Atsushi IkedaRegenerative & Cellular Medicine Kobe Center, Sumitomo Pharma Co., Ltd., Osaka, Japan.
Michael P SnyderDepartment of Genetics, Stanford University School of Medicine, Stanford, CA, USA.
Gen ShinozakiDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Palo Alto, CA, USA. gens@stanford.edu.ORCID http://orcid.org/0000-0001-6129-2789

Funding

Identification of Epigenetics Correlates between Brain and Peripheral TissuesR01MH119165 · NIMH · UNIVERSITY OF IOWA · PI SHINOZAKI, GEN · 2020 to 2024
$3.0M
U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) AG084710U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) R01 MH119165
6 · The paper itself

Abstract

Post-operative delirium (POD) is a serious complication of surgery particularly in older adults, characterized by acute disturbances in consciousness and cognition and associated with increased mortality and long-term cognitive impairment. Despite its clinical relevance, the underlying pathophysiology remains poorly understood. To address this, we performed multi-omics profiling of live brain tissue from patients undergoing neurosurgery. Single-nucleus RNA sequencing revealed POD-specific transcriptional alterations in glial cells, especially microglia, characterized by enhanced neuroinflammatory signatures. Astrocytes also exhibited changes in synaptic and migratory pathways. Upstream analysis implicated external cytokines as potential drivers of glial responses, while downstream analysis linked POD to encephalitis and dementia. DNA methylation profiling identified immune-related epigenetic alterations, suggesting a regulatory role in POD-associated neuroinflammation. Integration of bulk methylation and cell type-specific transcriptomic data suggested that epigenetic changes may influence gene expression during POD pathogenesis. These findings provide the convincing evidence of neuroinflammation and glial involvement as the pathophysiological mechanism of POD based on the first multi-omics analysis using patient brain tissue.

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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.