Evidence map›Paper›PMID 41733791›Full record

ArticleMolecular and cellular pediatrics2026

Soluble mucosal addressin cell adhesion molecule 1 is a biomarker for pediatric ulcerative colitis.

Moritz Muschaweck, Christian Gutbier, Gernot Sellge, Angeliki Pappa, Tobias Wenzl, Karim Hamesch, Norbert Wagner, Angela Schippers

Abstract read
In one paragraph

Article in Molecular and cellular pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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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

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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

8 authors.

Moritz MuschaweckDepartment of Pediatrics, RWTH Aachen University, Aachen, Germany. mmuschaweck@ukaachen.de.
Christian GutbierDepartment of Pediatrics, RWTH Aachen University, Aachen, Germany.
Gernot SellgeDepartment of Medicine III, RWTH Aachen University, Aachen, Germany.
Angeliki PappaDepartment of Pediatrics, RWTH Aachen University, Aachen, Germany.
Tobias WenzlDepartment of Pediatrics, RWTH Aachen University, Aachen, Germany.
Karim HameschDepartment of Medicine III, RWTH Aachen University, Aachen, Germany.
Norbert WagnerDepartment of Pediatrics, RWTH Aachen University, Aachen, Germany.
Angela SchippersDepartment of Pediatrics, RWTH Aachen University, Aachen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEnhanced expression of mucosal addressin cell adhesion molecule 1 (MAdCAM-1) on high endothelial venules facilitates lymphocyte migration to sites of intestinal inflammation in inflammatory bowel disease (IBD). This process may be accompanied by increased shedding of soluble MAdCAM-1 (sMAdCAM-1) from endothelial cells. Hence, circulating sMAdCAM-1 may serve as a biomarker of intestinal inflammation in IBD.

resultsThis single-center study enrolled pediatric (n = 32) and adult (n = 73) patients with IBD, as well as healthy controls (n = 56). Serum samples were collected from all participants, and sMAdCAM-1 concentrations were quantified using an ELISA assay. In healthy individuals, sMAdCAM-1 levels were highest in early childhood, declined during adolescence, and were lowest in adulthood. Concentrations of sMAdCAM-1 did not correlate with gut inflammation in pediatric or adult patients with Crohn’s disease (CD). In contrast, significantly increased sMAdCAM-1 levels were observed in adults with severe ulcerative colitis (UC). Moreover, sMAdCAM-1 levels distinguished healthy children from pediatric UC patients.

conclusionsThese findings provide new insights into sMAdCAM-1 as a marker of gut homeostasis and inflammation. Shedding of sMAdCAM-1 decreases during adolescence, and circulating sMAdCAM-1 levels could serve as a biomarker for ulcerative colitis in both pediatric and adult patients, particularly in severe disease.

Indexed as

BioassayInflammatory bowel diseaseLymphocyte migration

Identifiers

PMID41733791
PMCPMC12932750

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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.