Evidence map›Paper›PMID 40034792›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Peripheral blood mononuclear cell transcriptomic trajectories reveal dynamic regulation of inflammatory actors in delirium.

Sara C LaHue, Naoki Takegami, Rubinee Simmasalam, Abiya Baqai, Elena Munoz, Anya Sikri, Thibault du Buisson de Courson, Nilika S Singhal, Walter Eckalbar, Charles R Langelier and 14 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. 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.

Sara C LaHueDepartment of Neurology, School of Medicine, University of California-San Francisco (UCSF), USA.
Naoki TakegamiWeill Institute for Neurosciences, UCSF.
Rubinee SimmasalamDepartment of Neurology, School of Medicine, University of California-San Francisco (UCSF), USA.
Abiya BaqaiDepartment of Neurology, School of Medicine, University of California-San Francisco (UCSF), USA.
Elena MunozDepartment of Neurology, School of Medicine, University of California-San Francisco (UCSF), USA.
Anya SikriDepartment of Neurology, School of Medicine, University of California-San Francisco (UCSF), USA.
Thibault du Buisson de CoursonDepartment of Neurology, School of Medicine, University of California-San Francisco (UCSF), USA.
Nilika S SinghalDepartment of Neurology, School of Medicine, University of California-San Francisco (UCSF), USA.
Walter EckalbarDepartment of Medicine, UCSF.
Charles R LangelierDivision of Infectious Diseases, UCSF.
Carolyn M HendricksonDepartment of Medicine, UCSF.
Carolyn S CalfeeDepartment of Medicine, UCSF.
David J ErleDepartment of Medicine, UCSF.
Matthew F KrummelUCSF CoLabs, UCSF.
Prescott G WoodruffDepartment of Medicine, UCSF.
Tomiko OskotskyBakar Computational Health Sciences Institute, UCSF.ORCID 0000-0001-7393-5120
Marina SirotaBakar Computational Health Sciences Institute, UCSF.
Adam FergusonWeill Institute for Neurosciences, UCSF.
Vanja C DouglasDepartment of Neurology, School of Medicine, University of California-San Francisco (UCSF), USA.
John C NewmanBuck Institute for Research on Aging, Novato, USA.ORCID 0000-0002-8455-0100
Samuel J PleasureDepartment of Neurology, School of Medicine, University of California-San Francisco (UCSF), USA.
Michael R WilsonDepartment of Neurology, School of Medicine, University of California-San Francisco (UCSF), USA.ORCID 0000-0002-8705-5084
COMET consortium
Neel S SinghalDepartment of Neurology, School of Medicine, University of California-San Francisco (UCSF), USA.ORCID 0000-0003-1605-4444

Funding

Understanding Asthma EndotypesU19AI077439 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI David J Erle · 2008 to 2026
$41.1M
Humoral Immune Mechanisms of Acute and Chronic Neurologic Sequelae of COVID-19R01NS125693 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PLEASURE, SAMUEL JEREMY, WILSON, MICHAEL R · 2022 to 2025
$2.3M
NIAID NIH HHS U19 AI077439NINDS NIH HHS R01 NS125693
6 · The paper itself

Abstract

Delirium is a neurologic syndrome characterized by inattention and cognitive impairment frequently encountered in the medically ill. Peripheral inflammation is a key trigger of delirium, but the patient-specific immune responses associated with delirium development and resolution are unknown. This retrospective cohort study of prospectively collected biospecimens examines RNA sequencing from peripheral blood mononuclear cells of adults hospitalized for COVID-19 to better understand patient-specific factors associated with delirium (n = 64). Longitudinal transcriptomic analyses highlight persistent immune dysregulation in delirium, marked by increasing expression trajectories of genes linked to innate immune pathways, including complement activation, cytokine production, and monocyte/macrophage recruitment. Genes involved adaptive immunity showed a declining trajectory over time in patients with delirium. Although corticosteroid treatment suppressed some aspects of immune hyperactivation, aberrant responses contributing to delirium were exacerbated. Delirium resolution was characterized by normalization of key transcripts such as

Identifiers

PMID40034792
PMCPMC11875240

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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.