Evidence map›Paper›PMID 40608115›Full record

ArticlePediatric radiology2025

Baseline terminal ileal CT and MRI measurements are associated with imaging outcomes in pediatric Crohn's disease: a cohort study.

Allison D Ta, Jonathan R Dillman, Nicholas J Ollberding, Yael Haberman, Robert Baldassano, James Markowitz, Anthony Otley, Jennifer L Dotson, Marian Pfefferkorn, Jeffrey S Hyams and 7 more

Abstract readMulticenter Study
In one paragraph

Article in Pediatric radiology, 2025. 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

17 authors.

Allison D TaDepartment of Gastroenterology, Cincinnati Children's Medical Hospital Center, 3333 Burnett Ave, MLC 2010, Cincinnati, OH, 45229, USA. Allison.Ta@cchmc.org.ORCID 0000-0002-3403-5629
Jonathan R DillmanUniversity of Cincinnati College of Medicine, Cincinnati, OH, USA.
Nicholas J OllberdingUniversity of Cincinnati College of Medicine, Cincinnati, OH, USA.
Yael HabermanDepartment of Gastroenterology, Cincinnati Children's Medical Hospital Center, 3333 Burnett Ave, MLC 2010, Cincinnati, OH, 45229, USA.
Robert BaldassanoDepartment of Gastroenterology, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
James MarkowitzDepartment of Gastroenterology, Cohen Children's Medical Center of New York, New Hyde Park, NY, USA.
Anthony OtleyDepartment of Pediatrics, IWK Health Centre, Halifax, NS, Canada.
Jennifer L DotsonDepartment of Gastroenterology, Nationwide Children's Hospital, Columbus, OH, USA.
Marian PfefferkornDepartment of Gastroenterology, Indiana University School of Medicine, Indianapolis, IN, USA.
Jeffrey S HyamsDepartment of Gastroenterology, Connecticut Children's Medical Center, Hartford, CT, USA.
Melvin B HeymanDepartment of Gastroenterology, University of California San Francisco, San Francisco, CA, USA.
Sandra C KimDepartment of Gastroenterology, Cleveland Clinic Children's, Cleveland, OH, USA.
Joshua NoeDepartment of Gastroenterology, Medical College of Wisconsin, Milwaukee, WI, USA.
Scott SnapperDepartment of Gastroenterology, Boston Children's Hospital, Boston, MA, USA.
Adina AlazrakiDepartment of Radiology, Emory University and Children's Healthcare of Atlanta, Atlanta, GA, USA.
Subra KugathasanDepartment of Radiology, Emory University and Children's Healthcare of Atlanta, Atlanta, GA, USA.
Lee A DensonDepartment of Gastroenterology, Cincinnati Children's Medical Hospital Center, 3333 Burnett Ave, MLC 2010, Cincinnati, OH, 45229, USA.

Funding

Stem Cell/Organoid and Genome Editing CoreP30DK078392 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI Alexander Miethke · 2007 to 2026
$24.4M
PEDIATRIC GASTROENTEROLOGY AND NUTRITION TRAINING GRANTT32DK007727 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI Phillip P Minar · 1995 to 2026
$11.3M
Crohn's and Colitis Foundation of America 1P30DK078392-01NIDDK NIH HHS DK007727NIDDK NIH HHS P30 DK078392NIDDK NIH HHS T32 DK007727
6 · The paper itself

Abstract

backgroundCross-sectional imaging is increasingly used for both initial diagnosis and long-term monitoring of Crohn's disease. The quantitative morphology of the terminal ileum may predict treatment response.

objectiveWe aimed to identify baseline qualitative and quantitative imaging features that are associated with clinical and radiologic treatment response in a large cohort of children with Crohn's disease. MATERIALS AND

methodsThis was a retrospective study of the RISK cohort study in pediatric Crohn's disease. This multicenter study included 1,136 children <18 years from 28 sites in North America. Subjects enrolled with newly diagnosed Crohn's disease who underwent endoscopy with baseline and follow-up CT or MRI were considered for this study. Exclusion criteria were incomplete data or surgical resection prior to follow-up imaging. Imaging analysis included assessing a qualitative terminal ileum (TI) categorical score based on SAR-AGA consensus definitions ((1) normal, (2) inflammation only without luminal narrowing, (3) inflammation with luminal narrowing, or (4) stricture with pre-stenotic dilation ≥3 cm) and quantitative measurements (maximum bowel wall thickness and maximum/minimum lumen diameter). Two endpoints were considered: (1) clinical response (off corticosteroids and quiescent Physician Global Assessment at follow-up imaging) and (2) CT and MRI response (follow-up imaging normalization). Multivariable logistic regression analyses were developed for each endpoint.

resultsNinety-six subjects were included. Clinical response endpoint was achieved in 38% (n=36) of participants, and imaging normalization was achieved in only 20% (n=19) of participants. Follow-up imaging showed disease progression in 24 (25%) patients, 7 (7%) of whom were radiologically normal at baseline (7%). A higher baseline TI categorical score was associated with lower odds of imaging normalization during follow-up (OR 0.4 [0.2, 0.8], P=0.009). Larger TI minimum lumen diameter (OR 1.1 [1.01, 1.3], P=0.04) and smaller maximum bowel wall thickness at baseline (OR 0.8 [0.6, 0.97], P=0.03) were associated with imaging normalization. There were no baseline imaging measurements associated with clinical response.

conclusionsBaseline increased terminal ileal minimum lumen diameter and decreasing wall thickness were associated with imaging normalization at follow-up, but not clinical response.

Indexed as

Crohn DiseaseIleumMagnetic Resonance ImagingTomography, X-Ray ComputedAdolescentChildChild, PreschoolCohort StudiesFemaleHumansMaleRetrospective StudiesChildComputed tomographyCrohn’s diseaseLuminal narrowingMagnetic resonance enterographyPediatricQuantitative imagingStrictureTreatment response

Identifiers

PMID40608115
PMCPMC12321652

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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.