Cited by 66Celiac Disease Research and ManagementEosinophilic EsophagitisWheat and Barley Genetics and Pathology

Normalization Time of Celiac Serology in Children on a Gluten‐free Diet

Gidrewicz, Dominica, Trevenen, Cynthia L., Lyon, Martha, Butzner, J. Decker·2017·Journal of Pediatric Gastroenterology and Nutrition

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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Crossref · 10.1097/mpg.0000000000001270

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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).”

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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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