Fecal Gluten Peptides Reveal Limitations of Serological Tests and Food Questionnaires for Monitoring Gluten-Free Diet in Celiac Disease Patients.
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Comino Isabel, Fernández-Bañares Fernando, Esteve María, Ortigosa Luís, Castillejo Gemma, Fambuena Blanca, Ribes-Koninckx Carmen, Sierra Carlos, Rodríguez-Herrera Alfonso, Salazar José Carlos, Caunedo Ángel, Marugán-Miguelsanz J M, Garrote José Antonio, Vivas Santiago, Lo Iacono Oreste, Nuñez Alejandro, Vaquero Luis, Vegas Ana María, Crespo Laura, Fernández-Salazar Luis, Arranz Eduardo, Jiménez-García Victoria Alejandra, Antonio Montes-Cano Marco, Espín Beatriz, Galera Ana, Valverde Justo, Girón Francisco José, Bolonio Miguel, Millán Antonio, Cerezo Francesc Martínez, Guajardo César, Alberto José Ramón, Rosinach Mercé, Segura Verónica, León Francisco, Marinich Jorge, Muñoz-Suano Alba, Romero-Gómez Manuel, Cebolla Ángel, Sousa Carolina
Аннотация
METHODS: We performed a prospective, nonrandomized, multicenter study including 188 CD patients on GFD and 84 healthy controls. Subjects were given a dietary questionnaire and fecal GIP quantified by enzyme-linked immunosorbent assay (ELISA). Serological anti-tissue transglutaminase (anti-tTG) IgA and anti-deamidated gliadin peptide (anti-DGP) IgA antibodies were measured simultaneously.
RESULTS: Of the 188 celiac patients, 56 (29.8%) had detectable GIP levels in stools. There was significant association between age and GIP in stools that revealed increasing dietary transgressions with advancing age (39.2% in subjects ≥13 years old) and with gender in certain age groups (60% in men ≥13 years old). No association was found between fecal GIP and dietary questionnaire or anti-tTG antibodies. However, association was detected between GIP and anti-DGP antibodies, although 46 of the 53 GIP stool-positive patients were negative for anti-DGP.
CONCLUSIONS: Detection of gluten peptides in stools reveals limitations of traditional methods for monitoring GFD in celiac patients. The GIP ELISA enables direct and quantitative assessment of gluten exposure early after ingestion and could aid in the diagnosis and clinical management of nonresponsive CD and refractory CD. Trial registration number NCT02711397.