Normalization Time of Celiac Serology in Children on a Gluten‐free Diet
Abstract
Objectives: Response to a gluten‐free diet (GFD) in children with celiac disease is determined by symptom resolution and normalization of serology. We evaluated the rate of normalization of the transglutaminase (TTG) and antiendomysial (EMA) for children on a GFD after diagnosis. Methods: Celiac serologies were obtained over 3.5 years after starting a GFD in 228 newly diagnosed children with biopsy‐proven celiac disease. Patients were classified into categories based on serology (group A, TTG ≥10 × upper limit of normal [ULN] and EMA ≥ 1:80; group B, TTG ≥10 × ULN and EMA ⩽ 1:40; and group C, TTG <10 × ULN) and by severity of histologic injury at diagnosis. Results: In children with the highest serology at diagnosis (group A), 79.7% had an abnormal TTG at 12 months after diagnosis (mean TTG 12 months, 68.8 ± 7.3, normal <20 kU/L). At 2 years, an abnormal TTG persisted in 41.7%. In contrast, only 35% of children with the lowest serology at diagnosis (group C) displayed an abnormal TTG at 12 months (mean TTG 14.3 ± 1.9 kU/L). In those with the most severe mucosal injury, Marsh 3C, 74.2% and 33.2% had an abnormal TTG at 1 and 2 years. Conclusions: Normalization of celiac serology took >1 year in approximately 75% of GFD‐compliant children with the highest celiac serology or most severe mucosal injury at diagnosis. Clinicians must consider serology and histology at diagnosis to properly evaluate response to GFD.
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Full normalization of both TGA levels and histopathology may take over two years, particularly in those with severe small bowel lesions and high TGA levels at diagnosis.
“Full normalization of both TGA levels and histopathology may take over two years, particularly in those with severe small bowel lesions and high TGA levels at diagnosis (25-27).”
From ESPGHAN Position Paper on Management and Follow-up of Children and Adolescents With Celiac Disease. (2022) · cites this paper as [25]
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Charalampopoulos, D., Panayiotou, J., Chouliaras, G., Zellos, A., Kyritsi, E., & Roma, E. (2013) · European Journal of Clinical Nutrition · doi:10.1038/ejcn.2013.54 · Cited by 52 · see citing works
Vécsei, E., Steinwendner, S., Kogler, H., Innerhofer, A., Hammer, K., Haas, O. A., Amann, G., Chott, A., Vogelsang, H., Schoenlechner, R., et al. (2014) · BMC Gastroenterology · doi:10.1186/1471-230x-14-28 · Cited by 41 · see citing works
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ESPGHAN Position Paper on Management and Follow-up of Children and Adolescents With Celiac Disease.
Mearin, M. L., Agardh, D., Antunes, H., Al‐toma, A., Auricchio, R., Castillejo, G., Catassi, C., Ciacci, C., Discepolo, V., Dolinsek, J., et al. (2022) · Journal of pediatric gastroenterology and nutrition · doi:10.1097/mpg.0000000000003540 · Cited by 186 · see citing works
Sansotta, N., Alessio, M. G., Norsa, L., Previtali, G., Ferrari, A., Guerra, G., & D'Antiga, L. (2020) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/mpg.0000000000002519 · Cited by 31 · see citing works
- Authors
- Gidrewicz, D., Trevenen, C. L., Lyon, M., & Butzner, J. D.
- Affiliations
- University of Calgary (CA)
- Saskatchewan Health Authority (CA)
- Corresponding author
- Gidrewicz, Dominica
- Trevenen, Cynthia L.
- Butzner, J. Decker
- Venue
- Journal of Pediatric Gastroenterology and Nutrition
- Publisher
- Wiley
- Published
- 2017-03
- Volume
- 64
- Issue
- 3
- Pages
- 362-367
- ISSN
- 0277-2116 (ISSN-L)
- 1536-4801
- OpenAlex
- W2415838702
- Cited by
- 66
- References
- 2
- Citations by year
- 2026: 12 · 2025: 9 · 2024: 7 · 2023: 6 · 2022: 12 · 2021: 8 · 2020: 5 · 2019: 2 · 2018: 2 · 2017: 2
- FWCI
- 2.17
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Pediatric Gastroenterology and Nutrition (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Gastroenterology › Celiac Disease Research and Management
- Health Sciences › Medicine › Surgery › Eosinophilic Esophagitis
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Wheat and Barley Genetics and Pathology
- Keywords
- celiac disease, gluten-free diet, anti-tissue transglutaminase antibodies, anti-endomysial antibodies, children, Marsh classification, treatment response
- MeSH terms
- Protein Glutamine gamma Glutamyltransferase 2, Adolescent, Autoantibodies, Celiac Disease, Child, Child, Preschool, Female, Follow-Up Studies, Humans, Immunoglobulin A, Male, Transglutaminases, Retrospective Studies, Time Factors, Biomarkers, Treatment Outcome, GTP-Binding Proteins, Diet, Gluten-Free
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