Evidence map›Paper›PMID 30772585›Full record

ArticleClinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association2019

Association Between Level of Fecal Calprotectin and Progression of Crohn's Disease.

Nicholas A Kennedy, Gareth-Rhys Jones, Nikolas Plevris, Rebecca Patenden, Ian D Arnott, Charlie W Lees

Open access · hybridAbstract read
In one paragraph

Article in Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
9.0field-weighted citation impact, top 2% 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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 89 citations in OpenAlex.

  1. Pooled it
  2. Observational
  3. Factors Associated With Loss of Fecal Biomarker Accuracy During Routine Assessment of Inflammatory Bowel Disease.JGH open : an open access journal of gastroenterology and hepatology · 2026
    Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Observational
  9. Observational
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Biomarkers That Predict Crohn's Disease Outcomes.Journal of the Canadian Association of Gastroenterology · 2024
    Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Nicholas A KennedyInflammatory Bowel Disease Pharmacogenetics, University of Exeter, Exeter, United Kingdom; Gastrointestinal Unit, Western General Hospital, Edinburgh, United Kingdom; Gastrointestinal Unit, University of Edinburgh, Edinburgh, United Kingdom. Electronic address: n.kennedy@exeter.ac.uk.
Gareth-Rhys JonesGastrointestinal Unit, Western General Hospital, Edinburgh, United Kingdom; Gastrointestinal Unit, University of Edinburgh, Edinburgh, United Kingdom.
Nikolas PlevrisGastrointestinal Unit, Western General Hospital, Edinburgh, United Kingdom; Gastrointestinal Unit, University of Edinburgh, Edinburgh, United Kingdom.
Rebecca PatendenDepartment of Clinical Chemistry, Western General Hospital, Edinburgh, United Kingdom.
Ian D ArnottGastrointestinal Unit, Western General Hospital, Edinburgh, United Kingdom.
Charlie W LeesGastrointestinal Unit, Western General Hospital, Edinburgh, United Kingdom; Gastrointestinal Unit, University of Edinburgh, Edinburgh, United Kingdom.
Western General Hospital · GBUniversity of Exeter · GB

Funding

Wellcome Trust 097943Wellcome Trust 100469/Z/12/Z
6 · The paper itself

Abstract

BACKGROUND &

aimsMucosal healing is associated with improved outcomes in patients with Crohn's disease (CD), but assessment typically requires ileocolonoscopy. Calprotectin can be measured in fecal samples to determine luminal disease activity in place of endoscopy-this measurement is an important component of the treat-to-target strategy. We investigated whether levels of fecal calprotectin are associated with subsequent CD progression.

methodsWe performed a retrospective study of 918 patients with CD (4218 patient-years of follow-up evaluation; median, 50.6 mo; interquartile range [IQR], 32.8-76.0 mo) managed at a tertiary medical center in Edinburgh, United Kingdom, from 2003 through 2015. Patients were included if they had 1 or more fecal calprotectin measurements made 3 months or more after their diagnosis. We collected clinical data and fecal calprotectin measurements and analyzed these data to identify factors associated with a composite outcome of progression in Montreal behavior, hospitalization, and resection.

resultsAn increased level of fecal calprotectin at the index visit was associated with subsequent progression of CD, independent of symptoms or disease location. The median level of fecal calprotectin at the index visit was 432 μg/g (IQR, 1365-998 μg/g) in patients who reached the composite end point vs 180 μg/g (IQR, 50-665 μg/g) in patients who did not. In multivariable analysis, a cut-off value of 115 μg/g calprotectin identified patients who met the end point with a hazard ratio of 2.4 (95% CI, 1.8-3.1; P < .0001).

conclusionsIn a retrospective analysis of patients with CD, we found that measurements of fecal calprotectin made during routine monitoring can identify patients at risk for disease progression, independent of symptoms or disease location. It is therefore important to screen asymptomatic patients for mucosal inflammation and pursue complete resolution of inflammation.

Indexed as

AdultBiomarkersColonoscopyCrohn DiseaseDisease ProgressionFecesFemaleHumansLeukocyte L1 Antigen ComplexMaleMiddle AgedRetrospective StudiesSeverity of Illness IndexYoung AdultBiomarkersLeukocyte L1 Antigen ComplexBiomarkerIBDNoninvasivePrognostic Factor

Identifiers

PMID30772585
PMCPMC6880783
OpenAlexW2912905239

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.