Evidence map›Paper›PMID 42420838›Full record

ArticleBMC gastroenterology2026

FMT from Turkish patients with celiac disease is associated with celiac-like enteropathy features in a rat model.

Rugiyya Samadzade, Salih Macin, Babek Alibayov, Zeynep Celik, Mehmet Burak Ates, Muslu Kazım Korez, Huseyin Korkmaz, Duygu Findik

Abstract read
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Article in BMC gastroenterology, 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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0citing papers in PubMed
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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

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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

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Rugiyya SamadzadeDepartment of Medical Microbiology, Faculty of Medicine, Selcuk University, Konya, Turkey. rukiyesamadzade@gmail.com.ORCID https://orcid.org/0000-0002-7079-8500
Salih MacinDepartment of Medical Microbiology, Faculty of Medicine, Selcuk University, Konya, Turkey.
Babek AlibayovSchool of Advanced Technologies and Innovation Engineering, Western Caspian University, Baku, Azerbaijan.
Zeynep CelikDepartment of Pathology, Faculty of Veterinary Medicine, Selcuk University, Konya, Turkey.
Mehmet Burak AtesDepartment of Pathology, Faculty of Veterinary Medicine, Selcuk University, Konya, Turkey.
Muslu Kazım KorezDepartment of Biostatistics, Faculty of Medicine, Selcuk University, Konya, Turkey.
Huseyin KorkmazDepartment of Internal Medicine, Division of Gastroenterology, Faculty of Medicine, Selcuk University, Konya, Turkey.
Duygu FindikDepartment of Medical Microbiology, Faculty of Medicine, Selcuk University, Konya, Turkey. dfindik@selcuk.edu.tr.

Funding

Selçuk University Research Foundation 22212019
6 · The paper itself

Abstract

backgroundThis study investigated whether fecal microbiota transfer (FMT) from Turkish celiac disease (CD) patients is associated with the induction of celiac-like enteropathy features in a rat model.

methodsWistar rats received FMT from 10 CD patients or 10 healthy controls following microbiota depletion. Physiological, histopathological (Marsh-like classification), and inflammatory markers were evaluated.

resultsThe celiac disease fecal microbiota recipient rats (CD-FMT rats)group exhibited weight loss (p < 0.0001) and celiac-like histopathological features in 90% of cases. These included marked villous atrophy and intraepithelial lymphocyte counts > 20 per high-power field (HPF). A weighted kappa analysis (0.667) demonstrated a moderate association between donor Marsh scores and recipient histopathology. Systemic inflammation in the CD-FMT rats group was marked by a two-fold increase in serum IL-17 (~ 245 pg/ml; p < 0.0001) and a three-fold increase in IFN-γ (~ 95 pg/ml; p < 0.001). Additionally, mucosal mRNA expression of IL-15, IL-21, TNF-α, and IFN-α was upregulated approximately three-fold (p < 0.001). Serum β-actin levels were significantly elevated (~ 9.5 ng/ml; p < 0.0001), suggesting increased intestinal injury in this experimental setting.

conclusionFMT from Turkish CD patients was associated with the induction of celiac-like enteropathy features in this rat model. These findings suggest that gut microbiota from celiac disease patients may contribute to celiac-like mucosal and immune alterations in this experimental model, although it is not sufficient alone to induce disease and should be interpreted as a modulatory rather than causal factor.

Indexed as

Celiac DiseaseFecal Microbiota TransplantationActinsAdultAnimalsCytokinesDisease Models, AnimalFemaleHumansInterferon-alphaInterferon-gammaInterleukin-15Interleukin-17Interleukin-21InterleukinsIntestinal MucosaActinsCytokinesInterferon-alphaInterferon-gammaInterleukin-15Interleukin-17Interleukin-21InterleukinsRNA, MessengerTumor Necrosis Factor-alphaCeliac diseaseCytokinesFecal microbiota transferModelRatTurkish patients

Identifiers

PMID42420838
PMCPMC13629002

What Socratic holds

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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.