Evidence map›Paper›PMID 41969549›Full record

ReviewTranslational gastroenterology and hepatology2026

Conjugated bilirubin in chronic liver disease: an underutilised prognostic biomarker?-a narrative review.

Elise Fawcett, Aloysious D Aravinthan

Abstract readReview
In one paragraph

Review in Translational gastroenterology and hepatology, 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

2 authors.

Elise FawcettNIHR Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust and University of Nottingham, QMC Campus, Nottingham, UK.ORCID https://orcid.org/0009-0007-3396-0920
Aloysious D AravinthanNIHR Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust and University of Nottingham, QMC Campus, Nottingham, UK.ORCID https://orcid.org/0000-0003-0527-5137

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Objective: Chronic liver disease (CLD) is a major global health burden, often progressing to cirrhosis, decompensation, and hepatocellular carcinoma. Prognostic models typically rely on serum total bilirubin. However, recent evidence suggests that conjugated bilirubin (C-BIL) may offer superior prognostic utility in assessing disease severity and outcomes in CLD. This narrative review aims to examine the emerging evidence supporting C-BIL as a prognostic and disease stratification biomarker across various clinical contexts, where it has demonstrated enhanced predictive accuracy over traditional measures. Methods: A comprehensive, non-systematic review of the published literature was undertaken using major bibliographic databases and predefined keywords. Relevant studies were selected based on the following criteria: English-language publications, studies conducted in human populations, and articles with clear clinical applicability. Emphasis was placed on studies evaluating C-BIL in prognostic or disease-stratification contexts within CLD. Key Content and Findings: Emerging evidence indicates that incorporation of C-BIL into clinical prognostic models may enhance risk stratification and support more informed clinical decision-making in CLD. Elevated C-BIL appears to reflect impaired hepatocellular excretory function and fibrosis-related biliary obstruction. In addition, recent studies suggest that hepatocyte senescence may represent an additional, biologically plausible mechanism underpinning its prognostic relevance. Conclusions: This review highlights the potential clinical utility of C-BIL as a prognostic biomarker in CLD. While existing evidence supports its role in disease stratification and outcome prediction, further prospective validation and mechanistic studies are required before C-BIL can be adopted as a standard component of prognostic assessment in CLD.

Indexed as

Direct bilirubindisease stratificationhepatocyte senescence outcome predictionprognostication

Identifiers

PMID41969549
PMCPMC13066352

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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.