Glucometabolic Control and Anti-Transglutaminase Antibodies at Celiac Disease Onset in Type 1 Diabetes Youth - Summary - MDSpire

Glucometabolic Control and Anti-Transglutaminase Antibodies at Celiac Disease Onset in Type 1 Diabetes Youth

  • By

  • Francesca Di Candia

  • Francesco Maria Rosanio

  • Roberto Franceschi

  • Alessandro Fierro

  • Riccardo Bonfanti

  • Francesca Cardella

  • Valentino Cherubini

  • Giuseppe D’Annunzio

  • Barbara Felappi

  • Dario Iafusco

  • Brunella Iovane

  • Claudio Maffeis

  • Giulio Maltoni

  • Francesca Olivieri

  • Gabriele Olivieri

  • Barbara Piccini

  • Elvira Piccinno

  • Barbara Predieri

  • Ivana Rabbone

  • Maria Rossella Ricciardi

  • Giuseppina Salzano

  • Riccardo Schiaffini

  • Gianluca Tornese

  • Angela Zanfardino

  • Marco Marigliano

  • Riccardo Troncone

  • Riccardo Pertile

  • Luigi Greco

  • Renata Auricchio

  • Enza Mozzillo

  • ISPED Diabetes Study Group Collaborators

  • Francesco Gallo

  • Caterina Grosso

  • Carlo Ripoli

  • Fiorella De Berardinis

  • Susanna Coccoli

  • Valentina Tiberi

  • Sonia Toni

  • Maurizio Delvecchio

  • Rosanna Roppolo

  • Fortunato Lombardo

  • Stefano Passanisi

  • Bruno Bombaci

  • Alberto Casertano

  • Nicola Minuto

  • Marta Bassi

  • Evelina Maines

  • Silvia Savastio

  • Elena Inzaghi

  • Andrea Rigamonti

  • Giulio Frontino

  • Patrizia Bruzzi

  • Claudia Piona

  • November 4, 2025

  • 0 min

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Objective:

To correlate anti-TTG IgA titer, HbA1c at celiac disease diagnosis, and Marsh grade in children and adolescents with type 1 diabetes, emphasizing their interrelationships.

Key Findings:
  • HbA1c at celiac disease diagnosis was positively correlated with fold-anti-TTG IgA (Spearman r = 0.14, P = .0047).
  • Optimal anti-TTG IgA cutoff for sparing biopsy was determined to be 11 times the upper limit of normal.
  • T1D-CD individuals exhibited a higher prevalence of autoimmune comorbidities compared to T1D-only individuals (P < .001).
Interpretation:

Worse glucometabolic control in T1D-CD is associated with increased anti-TTG IgA levels and more severe mucosal damage, indicating the need for careful monitoring and potential adjustments in diagnostic criteria for celiac disease in clinical practice.

Limitations:
  • Retrospective design may introduce selection bias.
  • Data limited to a specific population in Italy, which may affect generalizability.
  • Potential confounding factors not accounted for in the analysis.
Conclusion:

Screening for celiac disease in youth with type 1 diabetes is crucial, especially given the higher prevalence of autoimmune comorbidities in those diagnosed with celiac disease before or concomitantly with type 1 diabetes. Specific recommendations for screening frequency should be considered.

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