Evidence map›Paper›PMID 41798956›Full record

ArticleFrontiers in immunology2026

The hidden link between iron deficiency and celiac disease: a clinical perspective.

Laura Tarancon-Diez, Guillermo Perez-Cabeza, Pilar Sanchez-Mingo, Pedro Crespo-de la Rosa, Rita-Maria Garcia, Marianela Iriarte-Gahete, Yolanda M Pacheco, Manuel Leal

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Article in Frontiers in immunology, 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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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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3 · Its place in the literature

Who cites it

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

8 authors.

Laura Tarancon-DiezPediatric Infections Group, Health Research Institute Gregorio Marañón (IiSGM), Madrid, Spain.
Guillermo Perez-CabezaEmergency Department, Hospital Viamed Santa Ángela de la Cruz, Seville, Spain.
Pilar Sanchez-MingoEurofins Hospital Viamed Santa Ángela de la Cruz, Seville, Spain.
Pedro Crespo-de la RosaServicio de Anatomia Patologica (SEVISTON), Hospital Viamed Santa Ángela de la Cruz, Seville, Spain.
Rita-Maria GarciaServicio de Anatomia Patologica (SEVISTON), Hospital Viamed Santa Ángela de la Cruz, Seville, Spain.
Marianela Iriarte-GaheteImmunology Service, Unit of Clinical Laboratories, Institute of Biomedicine of Seville, IBiS/Virgen del Rocío University Hospital/CSIC/University of Seville, Seville, Spain.
Yolanda M PachecoImmunology Service, Unit of Clinical Laboratories, Institute of Biomedicine of Seville, IBiS/Virgen del Rocío University Hospital/CSIC/University of Seville, Seville, Spain.
Manuel LealInternal Medicine Service, Hospital Viamed Santa Ángela de la Cruz, Seville, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Celiac disease (CD) is an immune-mediated enteropathy triggered by gluten ingestion in genetically predisposed individuals and represents a frequent but underdiagnosed cause of iron deficiency (ID). Screening for CD is recommended in unexplained ID, yet data on its prevalence among patients with absolute ID remain limited. This study aimed to determine the frequency of confirmed CD and Suspected Seronegative CD at Marsh 1 (SSCDM1) and to characterize their clinical, serological, histological, and immunogenetic profiles. Methods: A retrospective study was conducted within the ViaIron cohort including 86 individuals (≥14 years) with absolute ID (ferritin <50 ng/mL), with or without anemia, and no prior CD diagnosis. All underwent serological testing, duodenal biopsy with CD8 Results: Among 86 participants (93% female, median age 41 years), 14% had confirmed CD (Marsh 3) and 39.5% had SSCDM1. Only one-third of confirmed cases were seropositive, and 77% were asymptomatic. SSCDM1 patients closely resembled overt CD, showing low ferritin, hepcidin, and IgA levels but normal inflammatory markers, suggesting a shared malabsorption-driven, non-inflammatory mechanism of iron depletion. Autoimmune comorbidities, particularly autoimmune thyroiditis, and permissive HLA-DQ2/DQ8 haplotypes were highly frequent in both groups. Discussion: Nearly half of participants exhibited either overt or seronegative CD, revealing a continuum between both conditions. These findings highlight a frequently under-recognized, seronegative, immune-mediated duodenal injury consistent with possible gluten-sensitive enteropathy, which may escape detection by standard serological screening.

Indexed as

Celiac DiseaseIron DeficienciesAdolescentAdultBiopsyDuodenumFemaleGenotypeHLA-DQ AntigensHumansMaleMiddle AgedRetrospective StudiesYoung AdultHLA-DQ2 antigenHLA-DQ8 antigenHLA-DQ Antigensceliac diseaseduodenal biopsyHLA genotypingiron deficiencyseronegative celiac disease

Identifiers

PMID41798956
PMCPMC12960523

What Socratic holds

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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 Socratic graph.