Evidence map›Paper›PMID 32039369›Full record

ArticleJHEP reports : innovation in hepatology2019

Performance of the PRO-C3 collagen neo-epitope biomarker in non-alcoholic fatty liver disease.

Marie Boyle, Dina Tiniakos, Jorn M Schattenberg, Vlad Ratziu, Elisabetta Bugianessi, Salvatore Petta, Claudia P Oliveira, Olivier Govaere, Ramy Younes, Stuart McPherson and 6 more

Open access · goldAbstract read
In one paragraph

Article in JHEP reports : innovation in hepatology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 1 pooled it
11.3field-weighted citation impact, top 1% of its field
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

60 citing papers in PubMed, 1 synthesis or guideline pooled it, 130 citations in OpenAlex.

  1. Guideline
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  5. Dose-response effects on HbADiabetologia · 2024
    Trial
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  8. Article
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  12. Gene-based therapies for steatotic liver disease.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
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  14. Article
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  17. Review
  18. [Serological Markers to Assess Liver Fibrosis and Their Roles].The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi · 2024
    Review
  19. A roadmap for clinical trials in MASH-related compensated cirrhosis.Nature reviews. Gastroenterology & hepatology · 2024
    Review
  20. 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

16 authors at 10 institutions in 7 countries.

Marie BoyleNewcastle Liver Research Group, Institute of Cellular Medicine, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom.
Dina TiniakosNewcastle Liver Research Group, Institute of Cellular Medicine, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom.
Jorn M SchattenbergI. Department of Medicine, University Medical Centre, Mainz, Germany.
Vlad RatziuInstitute of Cardiometabolism and Nutrition, Pitié-Salpêtrière Hospital, Paris, France.
Elisabetta BugianessiDivision of Gastroenterology, Department of Medical Sciences, University of Torino, Torino, Italy.
Salvatore PettaSezione di Gastroenterologia, Di.Bi.M.I.S., University of Palermo, Italy.
Claudia P OliveiraDepartment of Gastroenterology, University of Sao Paulo School of Medicine, Sao Paulo, Brazil.
Olivier GovaereNewcastle Liver Research Group, Institute of Cellular Medicine, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom.
Ramy YounesNewcastle Liver Research Group, Institute of Cellular Medicine, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom.
Stuart McPhersonNewcastle Liver Research Group, Institute of Cellular Medicine, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom.
Pierre BedossaNewcastle Liver Research Group, Institute of Cellular Medicine, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom.
Mette J NielsenNordic Bioscience A/S, Biomarkers and Research, Herlev, Denmark.
Morten KarsdalNordic Bioscience A/S, Biomarkers and Research, Herlev, Denmark.
Diana LeemingNordic Bioscience A/S, Biomarkers and Research, Herlev, Denmark.
Stuart KendrickGlaxoSmithKline Research & Development Ltd, Stevenage, UK.
Quentin M AnsteeNewcastle Liver Research Group, Institute of Cellular Medicine, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom.
Newcastle University · GBNordic Bioscience (Denmark) · DKGlaxoSmithKline (United Kingdom) · GBJohannes Gutenberg University Mainz · DENewcastle upon Tyne Hospital · GBNIHR Newcastle Biomedical Research Centre · GBPitié-Salpêtrière Hospital · FRUniversidade de São Paulo · BRUniversity of Palermo · ITUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is an unmet need for non-invasive biomarkers in non-alcoholic fatty liver disease (NAFLD) that can diagnose advanced disease and identify patients suitable for clinical trials. The PRO-C3 collagen neo-epitope is a putative direct marker of fibrogenesis. We assessed the performance of PRO-C3 in a large, well-characterised international NAFLD cohort and report the development and validation of 2 novel panels for the diagnosis of advanced fibrosis (F≥3) in NAFLD, including a simplified clinical score which eliminates the need for online calculators.

methodsPlasma PRO-C3 levels were determined in a prospectively recruited international cohort of 449 patients with biopsy diagnosed NAFLD across the full disease spectrum (F0: n = 90; F1: 100; F2: 92; F3: 101; F4: 66). The cohort was divided into a discovery group (n = 151) and a validation group (n = 298). Logistic regression was performed to establish complex (FIBC3) and simplified (ABC3D) diagnostic scores that accurately identify advanced fibrosis. Performance for each was compared to established non-invasive fibrosis scoring systems.

resultsPlasma PRO-C3 levels correlated with grade of histological steatohepatitis (r

conclusionPlasma PRO-C3 levels correlate with severity of steatohepatitis and fibrosis stage. The FIBC3 panel is an accurate tool with a single threshold value that maintains both sensitivity and specificity for the identification of F≥3 fibrosis in NAFLD, eliminating indeterminate results and outperforming commonly used non-invasive tools. A greatly simplified version (ABC3D) that is readily amenable to use in the clinic has been validated and shown to perform with similar accuracy, and may prove a useful tool in routine clinical practice. LAY SUMMARY: We performed a comprehensive, independent evaluation of a collagen biomarker (PRO-C3) to detect and quantify liver fibrosis in patients with non-alcoholic fatty liver disease (NAFLD). We report the development of 2 diagnostic panels using PRO-C3 to identify patients with advanced fibrosis, one optimal but more complex to calculate (FIBC3), the other easier to use (ABC3D) whilst still performing well.

Indexed as

BiomarkerfibrosisNAFLDNASHPRO-C3Steatohepatitis

Identifiers

PMID32039369
PMCPMC7001575
OpenAlexW2953556757

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.