Esophagus to Small Intestine

Gut. 2025;74:918-925

Andersen IL, Lukina P, Dyrli OT, Klaasen RA, Warren DJ, Bolstad N, Mjønes P, Rønne E, Iversen R, Sollid LM, Lundin KEA, Ness-Jensen E

Serological screening for coeliac disease in an adult general population: The HUNT study


Background: A large proportion of individuals with coeliac disease (CeD) remain undiagnosed.
Objective: The aim of this study was to assess serological screening for CeD in the adult general population.
Design: The study was based on the fourth Trøndelag Health Study, a population-based study performed 2017–2019 in Nord-Trøndelag County, Norway, including 56,042 participants > 20 years of age (54% participation rate). Serum samples were analysed with a dual anti-transglutaminase 2 (TG2) IgA and IgG assay and seropositive participants were invited to endoscopy with duodenal biopsies. A CeD diagnosis was given if mucosal damage (Marsh grade 3) was found.
Results: Histological evaluation of 657 seropositive participants confirmed CeD in 423. The positive predictive value (PPV) of a positive TG2 IgA was 73.3% (95% confidence interval [CI]: 69.7–77.0%) for biopsy-confirmed CeD. TG2 IgA ≥ 10 times the upper limit of normal (ULN), as used in the no-biopsy approach in children, increased the PPV to 88.1% (95% CI: 84.8–91.4%). Primary TG2 IgG response was found in 87 participants, 5 of whom had biopsy-confirmed CeD. One of the participants with CeD primarily responding with TG2 IgG was IgA deficient. The PPV of a positive TG2 IgG was 5.8% (95% CI: 1.9–12.9%) and of TG2 IgG ≥ 10 x ULN was 9.5% (95% CI: 1.2–30.4%) for biopsy-confirmed CeD in TG2 IgA-negative individuals.

Conclusion: The dual anti-transglutaminase 2 (TG2) IgA assay showed excellent abilities as a screening tool for celiac disease (CeD) in the adult general population. However, the diagnostic accuracy of TG2 IgG was too poor for selectively identifying individuals with CeD.

I.L. Andersen, HUNT Research Centre, Department of Public Health and Nursing, NTNU, Norwegian University of Science and Technology, Levanger, Norway, E-Mail: ina.l.andersen@ntnu.no

DOI:  10.1136/gutjnl-2024-333886