Evidence map›Paper›PMID 40889075›Full record

ReviewIntensive care medicine experimental2025

Serum biomarkers of delirium in critical illness: a systematic review of mechanistic and diagnostic evidence.

Fergus O'Keeffe, Isolde Cervoni, Mario Ganau, Lara Prisco

Abstract readReview
In one paragraph

Review in Intensive care medicine experimental, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Observational
  6. Review
  7. Article
  8. Review
  9. Review
  10. Observational
  11. Article
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

4 authors.

Fergus O'KeeffeUniversity of Oxford, Oxford, UK.
Isolde CervoniThe Kennedy Institute of Rheumatology, University of Oxford, Oxford, UK.
Mario GanauNeurosurgery Department, John Radcliffe Hospital, Oxford, UK.
Lara PriscoNeurosciences Intensive Care Unit, John Radcliffe Hospital, Oxford, UK. Lara.prisco@ndcn.ox.ac.uk.ORCID http://orcid.org/0000-0001-6727-7870

Funding

National Institute for Health and Care Research NIHR 300741
6 · The paper itself

Abstract

Delirium is a frequent and serious complication of critical illness, yet its pathophysiological mechanisms remain incompletely understood. Serum biomarkers offer a potential avenue for improved diagnosis, risk stratification, and mechanistic insight. This systematic review synthesises evidence from 28 studies evaluating 54 serum biomarkers in relation to delirium among critically ill adult patients. Biomarkers were categorised by mechanistic pathway, including central nervous system (CNS) injury, immune activation, hormonal dysregulation, neurotransmission, coagulation, and amino acid metabolism. Among CNS injury markers, S100β and neurofilament light chain (NfL) demonstrated the most consistent associations with delirium presence and severity, supporting a role for astrocytic and axonal injury in delirium pathogenesis. Inflammatory markers such as interleukin-6 (IL-6), C-reactive protein (CRP), and tumour necrosis factor-alpha (TNF-α) were frequently studied but showed variable associations, reflecting the complex and non-specific nature of systemic inflammation. Hormonal biomarkers, including cortisol and prolactin, showed preliminary promise, while neurotransmitter-related biomarkers yielded inconsistent results, challenging canonical hypotheses. A major limitation in the literature was the lack of standardisation in delirium assessment, sampling timelines, and adjustment for confounding variables. Only a minority of studies incorporated temporal profiling or longitudinal outcomes, and replication across cohorts was limited. Heterogeneity in ICU populations further reduced generalisability. This review proposes a new conceptual framework of mechanistic endotyping, integrating multimodal biomarker profiling with clinical phenotyping to define biologically distinct subtypes of delirium. Such an approach may support precision medicine strategies by aligning therapeutic interventions with underlying pathophysiology. Future biomarker research should prioritise longitudinal sampling, harmonised protocols, and integration with EEG, imaging, and cognitive outcomes. Despite early promise, serum biomarkers for ICU delirium remain investigational and require further validation before clinical application.

Indexed as

BiomarkersCognitive impairmentDeliriumIntensive care unit

Identifiers

PMID40889075
PMCPMC12401822

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Registered trials

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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.