Deamidated gliadin peptide in pediatric patients with moderately increased tissue transglutaminase; does it help?

Jane A Dickerson1, Dale Lee2, M Cristina Pacheco3

  • 1Department of Laboratories, Seattle Children's Hospital, United States; Department of Laboratory Medicine, University of Washington, United States.

Insights

The deamidated gliadin peptide (DGP) screen is not specific enough to aid biopsy decisions in children with moderately elevated tissue transglutaminase (TTG) IgA levels. Further research is needed to establish its utility in pediatric celiac disease diagnosis.

Area of Science:

  • Pediatric gastroenterology
  • Immunology
  • Celiac disease diagnostics

Background:

  • Deamidated gliadin peptide (DGP) assays are emerging tools for celiac disease diagnosis and monitoring.
  • DGP IgG is recommended for children under 2, but its use in older pediatric populations is not well-established.
  • The diagnostic utility of the DGP screen (IgG + IgA) in conjunction with moderately elevated tissue transglutaminase (TTG) IgA levels remains unstudied.

Purpose of the Study:

  • To evaluate the specificity and utility of the DGP screen in pediatric patients with moderately elevated TTG IgA.
  • To determine if the DGP screen provides additional information to guide biopsy decisions in this patient group.

Main Methods:

  • Retrospective analysis of pediatric cases (January 2015 - October 2017) with TTG IgA levels between >19 and <100.
  • Collected data included DGP screen results and biopsy outcomes.
  • 31 out of 495 screened patients met the inclusion criteria.

Main Results:

  • The DGP screen demonstrated a sensitivity of 87.4% and a specificity of 56% in this cohort.
  • Specificity was notably lower in patients with diabetes.
  • The DGP screen did not significantly improve diagnostic accuracy for guiding biopsy decisions.

Conclusions:

  • The DGP screen lacks sufficient specificity to be a reliable tool for guiding biopsy decisions in pediatric patients with moderately elevated TTG IgA.
  • The findings suggest that the DGP screen does not offer substantial additional diagnostic value in this specific clinical scenario.
  • Further investigation may be warranted to explore the role of DGP in other pediatric celiac disease contexts.
Abstract

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