Evidence map›Paper›PMID 41860117›Full record

ArticleClinical and translational gastroenterology2026

Telomere Length in Celiac Disease in a Population-Based Cohort: A HUNT Study.

Reidar Fossmark, Henrik Hjorth-Hansen, Lisa Lirussi, Torben Lüders, Martina Visnovska, Yan Liu, Øyvind Salvesen, Hilde Loge Nilsen, Eivind Ness-Jensen

Abstract read
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Article in Clinical and translational 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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1 · What the graph read from it

What it found

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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

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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

9 authors.

Reidar FossmarkDepartment of Clinical and Molecular Medicine, NTNU, Trondheim, Norway.ORCID 0000-0002-5365-9357
Henrik Hjorth-HansenDepartment of Clinical and Molecular Medicine, NTNU, Trondheim, Norway.
Lisa LirussiDepartment of Microbiology, Oslo University Hospital, Norway.
Torben LüdersDepartment of Clinical Molecular Biology, University of Oslo and Akershus University Hospital.
Martina VisnovskaDepartment of Clinical Molecular Biology, University of Oslo and Akershus University Hospital.
Yan LiuDepartment of Clinical Molecular Biology, University of Oslo and Akershus University Hospital.
Øyvind SalvesenUnit of Applied Clinical Research, Department of Public Health and Nursing, NTNU, Trondheim, Norway.
Hilde Loge NilsenDepartment of Microbiology, Oslo University Hospital, Norway.
Eivind Ness-JensenHUNT Research Centre and HUNT Center for Molecular and Clinical Epidemiology, Department of Public Health and Nursing, NTNU, Levanger/Trondheim, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionCeliac disease (CeD) occurs in genetically predisposed individuals who are exposed to dietary gluten proteins. Genome-wide association studies have found CeD to be associated with a genetic predisposition to shorter telomere length. It was therefore of interest to measure leukocyte telomere length in a large cohort of patients with CeD.

methodsThis study was population-based and included a defined cohort of patients with CeD in the Trøndelag Health Study. Leukocyte telomere length was measured by quantitative polymerase chain reaction (PCR) in patients and controls 1:2 matched for age, sex, alcohol, and tobacco use.

resultsThe study population consisted of 58.7% women, with mean age 43 (SD 14.5) years, where half were never smokers, and the majority consumed little or no alcohol. Telomer length in 1,077 patients with CeD did not differ significantly from 2,147 matched controls, 10.39 kb (SD 2.21) vs 10.52 kb (SD 2.25), P = 0.088. In a mixed linear model, we found higher age and alcohol consumption, but not tobacco use or sex, to be associated with shorter telomere length. The telomere length did not differ between patients with newly diagnosed and known CeD. DISCUSSION: This large population-based study provides evidence that CeD is not associated with clinically meaningful telomere shortening.

Indexed as

Celiac DiseaseTelomereTelomere ShorteningAdultAgedAlcohol DrinkingCase-Control StudiesCohort StudiesFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansLeukocytesMaleMiddle AgedNorwayceliac diseasepopulation-basedtelomeres

Identifiers

PMID41860117
PMCPMC13641663

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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.