Evidence map›Paper›PMID 40419651›Full record

ArticleMolecular psychiatry2025

Whole-blood transcriptomic analysis reveals preoperative complement inhibitor deficiencies linked to postoperative delirium.

Occam Kelly Graves, Jiayi Kang, Haobo Li, Serkan Erdin, Matthew Smith, Ariel Mueller, Christopher Simon, Kwame Wiredu, Varun Bhave, Celine De Esch and 6 more

Abstract read
In one paragraph

Article in Molecular psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Trial
  2. Observational
  3. 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

16 authors.

Occam Kelly GravesMass General Brigham Department of Anesthesiology, Massachusetts General Hospital, Boston, MA, 02114, USA.ORCID http://orcid.org/0000-0003-3978-9750
Jiayi KangMass General Brigham Department of Anesthesiology, Massachusetts General Hospital, Boston, MA, 02114, USA.
Haobo LiMass General Brigham Department of Anesthesiology, Massachusetts General Hospital, Boston, MA, 02114, USA.
Serkan ErdinCenter for Genomic Medicine, Massachusetts General Hospital Research Institute, Boston, MA, 02114, USA.ORCID http://orcid.org/0000-0001-6587-2625
Matthew SmithMass General Brigham Department of Anesthesiology, Massachusetts General Hospital, Boston, MA, 02114, USA.
Ariel MuellerMass General Brigham Department of Anesthesiology, Massachusetts General Hospital, Boston, MA, 02114, USA.
Christopher SimonMass General Brigham Department of Anesthesiology, Massachusetts General Hospital, Boston, MA, 02114, USA.
Kwame WireduMass General Brigham Department of Anesthesiology, Massachusetts General Hospital, Boston, MA, 02114, USA.ORCID http://orcid.org/0000-0003-1519-1586
Varun BhaveHarvard Medical School, Boston, MA, 02115, USA.
Celine De EschCenter for Genomic Medicine, Massachusetts General Hospital Research Institute, Boston, MA, 02114, USA.
John LemanskiCenter for Genomic Medicine, Massachusetts General Hospital Research Institute, Boston, MA, 02114, USA.
Michael E TalkowskiCenter for Genomic Medicine, Massachusetts General Hospital Research Institute, Boston, MA, 02114, USA.
James RheeMass General Brigham Department of Anesthesiology, Massachusetts General Hospital, Boston, MA, 02114, USA.ORCID http://orcid.org/0000-0002-2181-4957
Jason QuMass General Brigham Department of Anesthesiology, Massachusetts General Hospital, Boston, MA, 02114, USA.
Tina B McKayMass General Brigham Department of Anesthesiology, Massachusetts General Hospital, Boston, MA, 02114, USA. tmckay@mgh.harvard.edu.ORCID http://orcid.org/0000-0003-0130-9272
Oluwaseun AkejuMass General Brigham Department of Anesthesiology, Massachusetts General Hospital, Boston, MA, 02114, USA. oluwaseun.akeju@mgh.harvard.edu.ORCID http://orcid.org/0000-0002-6740-1250

Funding

Pathophysiology of postoperative delirium and the use of biomimetic sleep as a treatment strategy in the CSICUR01AG053582 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI JOHNSON-AKEJU, OLUWASEUN · 2016 to 2020
$4.0M
Investigation of a Novel Biomarker of Postoperative DeliriumR21AG073750 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI JOHNSON-AKEJU, OLUWASEUN, MCKAY, TINA · 2022 to 2023
$462k
NIA NIH HHS R01 AG053582NIA NIH HHS R21 AG073750U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01AG053582U.S. Department of Health & Human Services | National Institutes of Health (NIH) R21AG073750
6 · The paper itself

Abstract

Postoperative delirium is a type of acute cognitive dysfunction characterized by inattention, disorganized thinking, and altered levels of consciousness that commonly develops after major surgery. Efforts to reduce the incidence of delirium have focused primarily on optimizing perioperative care, however the development of prophylactic interventions have been hindered by a limited understanding of the underlying mechanisms involved in delirium. In this secondary analysis of the Minimizing ICU Neurological Dysfunction with Dexmedetomidine-induced Sleep (MINDDS) trial, a nested case-control study (n = 51) was conducted using total RNA-sequencing analysis of whole-blood to investigate genes associated with delirium risk and development. Transcriptomic analysis revealed significantly lower expression of a key complement pathway inhibitor, C4BPA, in participants who experienced postoperative delirium. This finding was confirmed by quantitative PCR in the MINDDS cohort (n = 319) in adjusted logistic models. Furthermore, complement inhibitor CD55 was also found to be under-expressed in participants who developed delirium. Dexmedetomidine treatment modified associations between C4BPA and CD55 expression and the incidence of postoperative delirium by decreasing incidence in participants with low C4BPA and CD55 expression. This study revealed key complement regulators as risk biomarkers of postoperative delirium. Importantly, our findings suggest postoperative delirium risk is modifiable. Unlike previous research that has mainly focused on proteomics, this study underscores the effectiveness of whole-blood transcriptomics in identifying biomarkers and underlying biological mechanisms of postoperative delirium.

Indexed as

DeliriumPostoperative ComplicationsAgedBiomarkersCase-Control StudiesDexmedetomidineFemaleGene Expression ProfilingHumansIncidenceMaleMiddle AgedRisk FactorsTranscriptomeBiomarkersDexmedetomidine

Identifiers

PMID40419651
PMCPMC13332305

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