Evidence map›Paper›PMID 41640797›Full record

ArticleF1000Research2025

Histopathological Correlation in Suspected Celiac Disease: Linking Clinical, Serological, and Endoscopic Findings.

Genan AlMajed, Reem Alateeq, Sarah Bubshait, Manar Barnawi, Razan Almadani, Awadia Awadalla, Ahmed Alsayyah, Liqa Almulla

Abstract read
In one paragraph

Article in F1000Research, 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

8 authors.

Genan AlMajedImam Abdulrahman Bin Faisal University College of Medicine, Dammam, Eastern Province, Saudi Arabia.ORCID https://orcid.org/0009-0008-8357-5219
Reem AlateeqImam Abdulrahman Bin Faisal University College of Medicine, Dammam, Eastern Province, Saudi Arabia.ORCID https://orcid.org/0009-0002-3916-8284
Sarah BubshaitImam Abdulrahman Bin Faisal University College of Medicine, Dammam, Eastern Province, Saudi Arabia.
Manar BarnawiImam Abdulrahman Bin Faisal University College of Medicine, Dammam, Eastern Province, Saudi Arabia.ORCID https://orcid.org/0009-0005-6961-729X
Razan AlmadaniImam Abdulrahman Bin Faisal University College of Medicine, Dammam, Eastern Province, Saudi Arabia.ORCID https://orcid.org/0009-0007-1299-7943
Awadia AwadallaImam Abdulrahman Bin Faisal University College of Medicine, Dammam, Eastern Province, Saudi Arabia.
Ahmed AlsayyahImam Abdulrahman Bin Faisal University College of Medicine, Dammam, Eastern Province, Saudi Arabia.
Liqa AlmullaImam Abdulrahman Bin Faisal University College of Medicine, Dammam, Eastern Province, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Celiac disease (CD) is an immune-mediated enteropathy triggered by gluten in genetically susceptible individuals, characterized by villous atrophy, crypt hyperplasia, and intraepithelial lymphocytosis. Despite advances in serological testing, duodenal biopsy remains the diagnostic gold standard, especially in atypical or patchy disease. This retrospective study at King Fahd University Hospital (KFUH), Saudi Arabia, evaluated the diagnostic contribution of biopsies from the duodenal bulb (D1) and distal duodenum (D2) in 224 patients assessed for suspected CD between August 2023 and August 2024. Clinical, serological [IgA anti-tissue transglutaminase (anti-TG2), anti-endomysial antibodies (EMA), deamidated gliadin peptide], and histopathological data were analyzed. Sixty-five patients (29%) were diagnosed with CD. Villous atrophy, mucosal flattening, and increased intraepithelial lymphocytes were strongly associated with CD (p ≤ 0.001), and positive anti-TG2 and EMA correlated with Marsh grade. Combined D1 and D2 sampling improved diagnostic yield, underscoring the value of integrating histology and serology in evaluating classical and non-classical CD presentations.

Indexed as

Celiac DiseaseAdolescentAdultBiopsyChildDuodenumFemaleHumansMaleMiddle AgedRetrospective StudiesTransglutaminasesYoung AdultTransglutaminasesCeliac diseaseduodenal biopsyhistopathological correlationMarsh classificationserological markers

Identifiers

PMID41640797
PMCPMC12865290

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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.