Evidence map›Paper›PMID 41309136›Full record

ArticleInflammatory bowel diseases2026

Short Ileal Microvillus Length Phenotype Associates with Progression from Inflammatory to Complicated Disease Behavior in Pediatric Crohn's Disease.

Yael Haberman, Tzipi Braun, Rebekah Karns, Courtney A Bartel, Erin Bonkowski, Katherine F Simpson, Thomas D Walters, Jeffrey S Hyams, Ta-Chiang Liu, Subra Kugathasan and 2 more

Abstract read
In one paragraph

Article in Inflammatory bowel diseases, 2026. 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

5 · Who and what money

Authors and funding

12 authors.

Yael HabermanDivision of Gastroenterology, Hepatology, and Nutrition, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Tzipi BraunDepartment of Pediatrics, Sheba Medical Center, Tel-HaShomer, Tel-Aviv University, Tel-Aviv, Israel.
Rebekah KarnsDivision of Gastroenterology, Hepatology, and Nutrition, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Courtney A BartelDivision of Gastroenterology, Hepatology, and Nutrition, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Erin BonkowskiDivision of Gastroenterology, Hepatology, and Nutrition, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Katherine F SimpsonDepartment of Pathology and Immunology, Washington University in St Louis, St Louis, MO, United States.
Thomas D WaltersHospital for Sick Children, University of Toronto, Toronto, ON, Canada.
Jeffrey S HyamsConnecticut Children's Medical Center, Hartford, CT, United States.
Ta-Chiang LiuDepartment of Pathology and Immunology, Washington University in St Louis, St Louis, MO, United States.
Subra KugathasanDepartment of Pediatrics, Emory University and Children's Healthcare of Atlanta, Atlanta, GA, United States.ORCID 0000-0002-8686-4189
Lee A DensonDivision of Gastroenterology, Hepatology, and Nutrition, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Kelli L VanDussenDivision of Gastroenterology, Hepatology, and Nutrition, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.ORCID 0000-0002-5810-0720

Funding

Washington University DDRCC Supplemental Equipment RequestP30DK052574 · NIDDK · WASHINGTON UNIVERSITY · PI Jeffrey Wade Brown · 2000 to 2026
$30.8M
Stem Cell/Organoid and Genome Editing CoreP30DK078392 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI LEE ARMISTEAD DENSON · 2007 to 2026
$24.4M
Metabolic Benefits of Leptin ReductionR01DK127274 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI JOEL K. ELMQUIST, PHILIPP E SCHERER · 2021 to 2026
$5.1M
Dietary modulation of Paneth cellsR01DK136829 · NIDDK · WASHINGTON UNIVERSITY · PI Ta-Chiang Liu · 2023 to 2026
$2.1M
Paneth cell phenotype as a predictive biomarker for ulcerative colitisR01DK124274 · NIDDK · WASHINGTON UNIVERSITY · PI LIU, TA-CHIANG · 2020 to 2023
$1.5M
Cellular and molecular mechanisms of cigarette smoking-induced Paneth cell abnormalityR01DK125296 · NIDDK · WASHINGTON UNIVERSITY · PI LIU, TA-CHIANG · 2020 to 2023
$1.4M
Correction of Hearing and Vestibular Defects in a Mouse Model for DeafnessR01DC012596 · NIDCD · ROSALIND FRANKLIN UNIV OF MEDICINE & SCI · PI HASTINGS, MICHELLE L · 2013 to 2016
$1.3M
Durability of Epithelial Defects in Crohn's Disease IntestineR03DK124751 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI VANDUSSEN, KELLI LYNN · 2021 to 2022
$239k
Charitable Trust to Cincinnati Children's Hospital Medical CenterCincinnati Children's Research FoundationCincinnati Children's Research Foundation TrusteeCrohn's and Colitis Foundation Senior ResearchDigestive Diseases Research Core CenterERC 758313Integrative Morphology Core of the Digestive Diseases Research Core Center in CincinnatiIsrael Science Foundation 785/22NIDCD NIH HHS R01 DC012596NIDDK NIH HHS P30 DK052574NIDDK NIH HHS P30 DK078392NIDDK NIH HHS R01 DK124274NIDDK NIH HHS R01 DK125296NIDDK NIH HHS R01 DK127274NIDDK NIH HHS R01 DK136829NIDDK NIH HHS R03 DK124751NIH HHS P30 DK052574NIH HHS P30 DK078392NIH HHS R01 DK124274NIH HHS R01 DK125296NIH HHS R01 DK136829NIH HHS R03 DK124751The Helmsley Charitable Trust to Sheba Medical CenterThe Helmsley Charitable Trust to Washington University in St. LouisWashington University in St. Louis
6 · The paper itself

Abstract

BACKGROUND AND

aimsOur previous studies of adult Crohn's disease (CD) suggested ileal microvillus length (MVL) as a prognostic biomarker for therapy response. We investigated if ileal MVL also differed in pediatric CD versus controls and tested for associations with stricturing or penetrating disease behavior outcomes.

methodsWe determined the average ileal MVL of 412 CD and 88 control H&E-stained ileal histology samples from a subset of the RISK cohort and 2 validation cohorts. The RISK sub-cohort had an average follow-up of >60 months and was used to test for associations between ileal MVL and clinical data, RNA-seq molecular profiles, and histopathological scores.

resultsIleal MVL was shorter in CD relative to control (median of 1.396 µm vs. 1.598 µm, respectively). Ileal MVL generally did not associate with demographics or clinical disease activity indices. However, there was a significant association between shorter ileal MVL and increased risk of development of complicated disease behavior. Furthermore, CD samples with shorter ileal MVL showed a significantly shorter time to development of complicated disease behavior. Ileal MVL positively associated with a gene signature enriched for brush border membrane and negatively associated with a gene signature enriched for extracellular matrix, inflamed macrophages, and fibroblasts. Accordingly, ileal MVL was negatively correlated with histopathological scores.

conclusionsShort ileal MVL is associated with the development of complicated disease behaviors in pediatric CD, supporting the potential use of this histological phenotype as a biomarker for CD prognosis.

Indexed as

Crohn DiseaseIleumAdolescentBiomarkersCase-Control StudiesChildDisease ProgressionFemaleFollow-Up StudiesHumansMalePhenotypePrognosisBiomarkersbiomarkerbrush borderCrohn’s diseasehistopathologyprognosis

Identifiers

PMID41309136
PMCPMC12695081

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.