Evidence map›Paper›PMID 33351719›Full record

ArticleUnited European gastroenterology journal2021

Elevated ectodomain of type 23 collagen is a novel biomarker of the intestinal epithelium to monitor disease activity in ulcerative colitis and Crohn's disease.

T Manon-Jensen, S Sun, M Lindholm, V Domislović, P Giuffrida, M Brinar, G Mazza, M Pinzani, Z Krznarić, A Di Sabatino and 2 more

Open access · hybridAbstract read
In one paragraph

Article in United European gastroenterology journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

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  9. UEGWeek: The modern School of Athens.United European gastroenterology journal · 2021
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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

12 authors at 4 institutions in 5 countries.

T Manon-JensenInstitute for Liver and Digestive Health, University College of London, London, UK.
S SunInstitute for Liver and Digestive Health, University College of London, London, UK.
M LindholmInstitute for Liver and Digestive Health, University College of London, London, UK.
V DomislovićBiomarkers and Research, Nordic Bioscience, Herlev, Denmark.ORCID 0000-0002-3715-5730
P GiuffridaDepartment of Gastroenterology and Hepatology, Clinical Hospital Centre, Zagreb, Croatia.
M BrinarBiomarkers and Research, Nordic Bioscience, Herlev, Denmark.
G MazzaFirst Department of Internal Medicine, University of Pavia, Pavia, Italy.
M PinzaniFirst Department of Internal Medicine, University of Pavia, Pavia, Italy.
Z KrznarićBiomarkers and Research, Nordic Bioscience, Herlev, Denmark.
A Di SabatinoDepartment of Gastroenterology and Hepatology, Clinical Hospital Centre, Zagreb, Croatia.ORCID 0000-0002-0302-8645
M A KarsdalInstitute for Liver and Digestive Health, University College of London, London, UK.
J H MortensenInstitute for Liver and Digestive Health, University College of London, London, UK.
Institute for Liver Health · USNordic Bioscience (Denmark) · DKUniversity Hospital Centre Zagreb · HRUniversity of Pavia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImpaired intestinal epithelial barrier is highly affected in inflammatory bowel disease. Transmembrane collagens connecting the epithelial cells to the extracellular matrix have an important role in epithelial cell homeostasis. Thus, we sought to determine whether the transmembrane type 23 collagen could serve as a surrogate marker for disease activity in patients with Crohn's disease and ulcerative colitis.

methodsWe developed an enzyme-linked immunosorbent assay to detect the ectodomain of type 23 collagen (PRO-C23) in serum, followed by evaluation of its levels in both acute and chronic dextran sulphate sodium colitis models in rats and human inflammatory bowel disease cohorts. Serum from 44 Crohn's disease and 29 ulcerative colitis patients with active and inactive disease was included.

resultsIn the acute and chronic dextran sulphate sodium-induced rat colitis model, the PRO-C23 serum levels were significantly increased after colitis and returned to normal levels after disease remission. Serum levels of PRO-C23 were elevated in Crohn's disease (p < 0.05) and ulcerative colitis (p < 0.001) patients with active disease compared to healthy donors. PRO-C23 differentiated healthy donors from ulcerative colitis (area under the curve [AUC]: 0.81, p = 0.0009) and Crohn's disease (AUC: 0.70, p = 0.0124). PRO-C23 differentiated ulcerative colitis patients with active disease from those in remission (AUC: 0.75, p = 0.0219) and Crohn's disease patients with active disease from those in remission (AUC: 0.68, p = 0.05).

conclusionPRO-C23 was elevated in rats with active colitis, and inflammatory bowel disease patients with active disease. Therefore, PRO-C23 may be used as a surrogate marker for monitoring disease activity in ulcerative colitis and Crohn's disease.

Indexed as

AdultAnimalsAntibodiesBiomarkersColitis, UlcerativeCollagenCrohn DiseaseDextran SulfateDisease Models, AnimalEnzyme-Linked Immunosorbent AssayFemaleHumansIntestinal MucosaMaleMiddle AgedRatsAntibodiesBiomarkersCOL23A1 protein, humanCollagenDextran Sulfatecollagenepitheliuminflammatory bowel diseaseserological biomarker

Identifiers

PMID33351719
PMCPMC8259268
OpenAlexW3115436403

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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.