Evidence map›Paper›PMID 41195622›Full record

Observational studyJournal of pediatric gastroenterology and nutrition2026

Bulb biopsies for diagnosing celiac disease in children: A prospective multicenter study using quantitative histomorphometry.

Alina Popp, Juha Taavela, Taina Arvola, Katri Kaukinen, Markku Mäki, Kalle Kurppa

Registry-linked trialAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Journal of pediatric gastroenterology and nutrition, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02072590 (Improved Diagnostics of Celiac Disease in Children), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

NCT02072590 completednot on this map

Improved Diagnostics of Celiac Disease in Children

TypeobservationalSponsorTampere University HospitalRan2011 to 2023Enrolled300ConditionsCeliac Disease, Eosinophilic Esophagitis
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Observational
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

6 authors.

Alina PoppCeliac Disease Research Center, Faculty of Medicine and Health Technology, Tampere University and Tampere University Hospital, Wellbeing Services County of Pirkanmaa, Tampere, Finland.
Juha TaavelaCeliac Disease Research Center, Faculty of Medicine and Health Technology, Tampere University and Tampere University Hospital, Wellbeing Services County of Pirkanmaa, Tampere, Finland.
Taina ArvolaDepartment of Pediatrics, Hospital District of Kanta-Häme, Hämeenlinna, Finland.
Katri KaukinenCeliac Disease Research Center, Faculty of Medicine and Health Technology, Tampere University and Tampere University Hospital, Wellbeing Services County of Pirkanmaa, Tampere, Finland.
Markku MäkiCeliac Disease Research Center, Faculty of Medicine and Health Technology, Tampere University and Tampere University Hospital, Wellbeing Services County of Pirkanmaa, Tampere, Finland.
Kalle KurppaCeliac Disease Research Center, Faculty of Medicine and Health Technology, Tampere University and Tampere University Hospital, Wellbeing Services County of Pirkanmaa, Tampere, Finland.ORCID https://orcid.org/0000-0003-4757-2164

Funding

Foundation for Pediatric Researchthe Finnish Celiac Societythe Sigrid Juselius Foundationthe State Funding for University-level Health Research, Tampere University Hospital, Wellbeing Services County of Pirkanmaa
6 · The paper itself

Abstract

objectivesDuodenal bulb specimens are recommended for the diagnostic evaluation of celiac disease (CeD). However, it remains unclear if their quality and histomorphometry measures are comparable to samples obtained from the distal duodenum. We investigated this issue, as well as the diagnostic applicability of morphometry and advanced immunohistochemistry methods, in a prospective pediatric cohort using validated morphometric readouts.

methodsOne hundred ninety-four children with CeD autoantibodies underwent systematic sampling at diagnosis from bulb and distal duodenum. Morphometric evaluation included measurements of villous height (VH), crypt depth (CrD), and VH:CrD. Mucosal CD3+ and γδ+ intraepithelial lymphocytes (IEL) densities and transglutaminase-2-targeted immunoglobulin A (IgA) deposits were measured from frozen biopsies. Sixteen seronegative non-CeD children served as controls.

resultBulb specimens were frequently of inadequate quality, with paired comparisons to distal samples feasible in only 112 patients. Mean VH and VH:CrD were lower in the bulb than in the distal duodenum (168 vs. 239 μm, p < 0.001; 0.73 vs. 1.01, p = 0.027, respectively), while CrDs and IEL densities were comparable. Twelve patients had reduced VH:CrD consistent with CeD in the bulb only. Eight seropositive children exhibited normal VH:CrD in both bulb and distal duodenal samples, but the presence of positive γδ + IELs and IgA deposits indicated incipient CeD. Overall, 96.4% of the patients and none of the controls had IgA deposits in both bulb and distal samples.

conclusionsA subgroup of patients had diagnostic lesions only in the bulb, but discretion is needed, as these specimens may be of poorer quality and different histomorphometric measurements compared to distal samples. The determination of IgA deposits is valuable at both duodenal sites. CLINICAL

trial registrationThis study is registered at ClinicalTrials.gov (registration number NCT02072590). The study was registered in February 2014, while patient enrollment began in January 2012. At the time of study initiation, mandatory prospective trial registration was not yet widely enforced for nonpharmaceutical, investigator-initiated clinical studies.

Indexed as

Celiac DiseaseDuodenumIntestinal MucosaAdolescentAutoantibodiesBiopsyChildChild, PreschoolFemaleHumansImmunoglobulin AImmunohistochemistryInfantMaleProspective StudiesAutoantibodiesImmunoglobulin Adepositsdiagnosishistologymorphologysmall bowel

Identifiers

PMID41195622
PMCPMC12780468

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Registered trials

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.