Evidence map›Paper›PMID 31058681›Full record

Observational studyThe American journal of gastroenterology2019

Serum Protein Biomarkers of Fibrosis Aid in Risk Stratification of Future Stricturing Complications in Pediatric Crohn's Disease.

Jing Wu, David M Lubman, Subra Kugathasan, Lee A Denson, Jeffrey S Hyams, Marla C Dubinsky, Anne M Griffiths, Robert N Baldassano, Joshua D Noe, Shervin Rabizadeh and 5 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in The American journal of gastroenterology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 2 pooled it
–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

31 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Biomarkers for the Prediction and Diagnosis of Fibrostenosing Crohn's Disease: A Systematic Review.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2022
    Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Challenges in IBD Research 2024: Novel Technologies.Inflammatory bowel diseases · 2024
    Review
  11. Review
  12. Anti-fibrotics in inflammatory bowel diseases: Challenges and successes.Advances in pharmacology (San Diego, Calif.) · 2024
    Review
  13. Article
  14. How to Evaluate Fibrosis in IBD?Diagnostics (Basel, Switzerland) · 2023
    Review
  15. Big Data in Gastroenterology Research.International journal of molecular sciences · 2023
    Review
  16. Multi-omics in Crohn's disease: New insights from inside.Computational and structural biotechnology journal · 2023
    Review
  17. Article
  18. Article
  19. Article
  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

15 authors.

Jing WuDepartment of Surgery, University of Michigan, Ann Arbor, Michigan, USA.
David M LubmanDepartment of Surgery, University of Michigan, Ann Arbor, Michigan, USA.
Subra KugathasanDivision of Pediatric Gastroenterology, Department of Pediatrics, Emory University School of Medicine, Atlanta, Georgia, USA.
Lee A DensonDivision of Pediatric Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Cincinnati Children's Hospital Medical Center and the University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.
Jeffrey S HyamsDivision of Digestive Diseases, Hepatology, and Nutrition, Department of Pediatrics, Connecticut Children's Medical Center, Hartford, Connecticut, USA.
Marla C DubinskyDepartment of Pediatrics, Division of Gastroenterology and Nutrition, Icahn School of Medicine, Mount Sinai New York, New York, USA.
Anne M GriffithsDivision of Pediatric Gastroenterology, Hepatology and Nutrition, Department of Pediatrics, the Hospital for Sick Children, University of Toronto, Toronto, Canada.
Robert N BaldassanoDivision of Pediatric Gastroenterology, Department of Pediatrics, Children's Hospital of Pennsylvania, Philadelphia, Pennsylvania, USA.
Joshua D NoeDivision of Pediatric Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Shervin RabizadehDivision of Pediatric Gastroenterology, Department of Pediatrics, Cedars-Sinai Medical Center, Los Angeles, California, USA.
Ajay S GulatiDivision of Pediatric Gastroenterology, Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Joel R RoshDepartment of Pediatrics, Goryeb Children's Hospital, Morristown, New Jersey, USA.
Wallace V CrandallDivision of Pediatric Gastroenterology, Department of Pediatrics, Nationwide Children's Hospital, the Ohio State University College of Medicine, Columbus, Ohio, USA.
Peter D R HigginsDivision of Gastroenterology and Hepatology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Ryan W StidhamDivision of Gastroenterology and Hepatology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.

Funding

Stem Cell/Organoid and Genome Editing CoreP30DK078392 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI Alexander Miethke · 2007 to 2026
$24.4M
University of Michigan Center for Gastrointestinal ResearchP30DK034933 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI OMARY, BISHR · 1986 to 2021
$22.5M
Improving Prediction of Medical Responsiveness and Clinical Outcomes in Crohn's DiseaseK23DK101687 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI STIDHAM, RYAN WILLIAM · 2015 to 2019
$945k
NIDDK NIH HHS K23 DK101687NIDDK NIH HHS P30 DK034933NIDDK NIH HHS P30 DK078392
6 · The paper itself

Abstract

objectivesAvoiding fibrostenotic complications is of paramount concern in the management of Crohn's disease (CD). We sought to investigate the association of candidate biomarkers of fibrosis collected at diagnosis with the future development of fibrostenotic CD.

methodsUsing the Risk Stratification and Identification of Immunogenetic and Microbial Markers of Rapid Disease Progression in Children with Crohn's Disease cohort, a multicenter prospective observational pediatric inception cohort, subjects with an inflammatory phenotype (B1) at diagnosis who later converted to a stricturing phenotype (B2) within 3 years were compared with those who remained B1. Serum collected at diagnosis underwent both parallel reaction monitoring-targeted proteomic analysis and conventional enzyme-linked immunosorbent assay for 10 candidate biomarkers of intestinal fibrosis. Cox proportional hazard regression was used for multivariable analysis of time-dependent outcomes.

resultsIn 116 subjects 58 subjects with verified B1 phenotype at diagnosis who later converted to B2 disease were compared with 58 subjects who remained B1 over 3 years of follow-up. Extracellular matrix protein 1 (ECM1) levels in the upper quartile (hazard ratio [HR] 3.43, 95% confidence limit [CL] 1.33, 8.42) were associated with future fibrostenotic disease. ASCA IgA (HR 4.99, 95% CL 1.50, 16.68) and CBir levels (HR 5.19, 95% CL 1.83, 14.74) were also associated with future intestinal fibrostenosis, although ECM1 continued to demonstrate independent association with conversion to B2 even with adjustment for serologies in multivariable analysis (HR 5.33, 95% CL 1.29, 22.13).

conclusionsECM1 and other biomarkers of fibrosis may aid in determining the risk of uncomplicated inflammatory disease converting to B2 stricturing phenotypes in children with CD. Prospective validation studies to verify test performance and optimize clinical utilization are needed before clinical implementation.

Indexed as

Crohn DiseaseIntestinesBiomarkersChildConstriction, PathologicDisease ProgressionExtracellular Matrix ProteinsFemaleFibrosisHumansInflammationMaleProteomicsRisk AssessmentBiomarkersECM1 protein, humanExtracellular Matrix Proteins

Identifiers

PMID31058681
PMCPMC6532424

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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.