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Monitoring patients with celiac disease on gluten free diet: different outcomes comparing three tissue transglutaminase IgA assays

Authors :
Mulder, A H Leontine
Castelijn, Daan A R
van der Pol, Pieter
Vermeer, Marloes
Hollander, Jolien C
Kuiper, Tietie
Bijnens, Caroline
Bontkes, Hetty J
Damoiseaux, Jan
Mulder, A H Leontine
Castelijn, Daan A R
van der Pol, Pieter
Vermeer, Marloes
Hollander, Jolien C
Kuiper, Tietie
Bijnens, Caroline
Bontkes, Hetty J
Damoiseaux, Jan
Source :
Clinical Chemistry and Laboratory Medicine vol.62 (2024) date: 2024-03-01 nr.4 p.674-681 [ISSN 1434-6621]
Publication Year :
2024

Abstract

Objectives: Tissue transglutaminase (tTG) IgA antibodies are a hallmark for celiac disease (CD). In CD patients on gluten free diet (GFD) these antibodies are transient. Few studies are available comparing the tTG-IgA assay characteristics for monitoring response to GFD. Since discrepant results were reported in patients on GFD after switching tTG-IgA assays, we conducted a retrospective observational study to monitor GFD response using three different tTG-IgA assays. Methods: Diagnostic samples from 44 adults and 17 children with CD were included. Of most patients two follow-up samples after introduction of GFD were available. In all samples tTG-IgA were assessed using one fluorochrome-enzyme immuno-assay (FEIA) and two chemiluminescence immuno-assays (CLIA) and intestinal fatty acid binding protein (i-FABP) as surrogate marker for intestinal epithelial damage was measured. Results: Using CLIA assays, normalization of antibody levels was delayed compared to FEIA (p<0.001). Of all samples taken after at least 6months on GFD with elevated i-FABP indicating intestinal epithelial damage, 40% had positive tTG-IgA according to the FEIA, 85 and 90% according to the two CLIA. Conclusions: Normalization of tTG-IgA in patients on GFD depends on the assay used. Both CLIA appear to be more sensitive in detecting suboptimal treatment response in CD-indicated by elevated i-FABP - when applying the manufacturer's recommended cut-off for the diagnosis of CD.

Details

Database :
OAIster
Journal :
Clinical Chemistry and Laboratory Medicine vol.62 (2024) date: 2024-03-01 nr.4 p.674-681 [ISSN 1434-6621]
Notes :
DOI: 10.1515/cclm-2023-1076, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1434553496
Document Type :
Electronic Resource