Evidence map›Paper›PMID 37788094›Full record

ArticleAmerican journal of clinical pathology2024

A tip-predominant distribution of villous intraepithelial lymphocytes is not specific to celiac disease in children with Marsh I lesions.

Denis Chang, Charlotte F Kim, Maxwell Horton, Dale Lee, M Cristina Pacheco, Jocelyn A Silvester, Jeffrey D Goldsmith

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in American journal of clinical pathology, 2024. 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
0.3field-weighted citation impact, top 39% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

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

7 authors at 3 institutions in 1 country.

Denis ChangHarvard Celiac Research Program, Harvard Medical School, Boston, MA, US.ORCID 0000-0002-3843-5785
Charlotte F KimDepartment of Pathology and Immunology, Texas Children's Hospital, Houston, TX, US.
Maxwell HortonHarvard Celiac Research Program, Harvard Medical School, Boston, MA, US.
Dale LeeDivision of Pediatric Gastroenterology and Hepatology, Seattle Children's Hospital, Seattle, WA, US.
M Cristina PachecoDepartment of Laboratory Medicine and Pathology, Seattle Children's Hospital, Seattle, WA, US.
Jocelyn A SilvesterHarvard Celiac Research Program, Harvard Medical School, Boston, MA, US.
Jeffrey D GoldsmithHarvard Celiac Research Program, Harvard Medical School, Boston, MA, US.
Boston Children's Hospital · USSeattle Children's Hospital · USTexas Children's Hospital · US

Funding

Mechanisms and Markers of Small Intestinal Epithelial Injury and Villous AtrophyK23DK119584 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI SILVESTER, JOCELYN ANNE · 2019 to 2023
$971k
NIDDK NIH HHS K23 DK119584NIH HHS K23DK119584
6 · The paper itself

Abstract

objectivesTo assess if the distribution of villous intraepithelial lymphocytes (IELs) in a pediatric cohort with Marsh I histopathology is specific to celiac disease (CeD).

methodsMulticenter, retrospective case-control study between January 2001 and December 2019 in children (<18 years) with and without CeD with intraepithelial lymphocytosis and normal villous architecture. Pathology specimens were reviewed by 2 study pathologists who were blinded to the final diagnosis. Morphologic features (villous height to crypt depth ratio [Vh:Cd]) and IELs in the villous tip, top, or bottom half of the villus were quantified.

resultsOf the 97 children with Marsh I histopathology identified during the study period, 63 were excluded due to an insufficient number of well-oriented villous-crypt complexes or a Vh:Cd less than 2. Villous IELs were measured in 34 cases (14 CeD, 20 non-CeD controls). There was no difference between the non-CeD and CeD groups in the mean IELs at the villous tip (14.0 ± 7.1 vs 11.7 ± 6.0, P = .31), top (46.4 ± 18.4 vs 38.3 ± 10.8, P = .11), or bottom (29.8 ± 16.8 vs 28.5 ± 12.8, P = .80) half of each villus, respectively.

conclusionsThe distribution of IELs in Marsh I lesions is not specific for CeD.

Indexed as

Celiac DiseaseIntraepithelial LymphocytesLymphocytosisBiopsyCadmiumCase-Control StudiesChildDuodenumHumansIntestinal MucosaLymphocytesRetrospective StudiesWetlandsCadmiumceliac diseaseintraepithelial lymphocytosisMarsh Ipediatricvillous tip

Identifiers

PMID37788094
PMCPMC10833141
OpenAlexW4387300135

What OpenQuestion holds

Textmetadata
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.