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Exposure Sources, Amounts and Time Course of Gluten Ingestion and Excretion in Patients with Coeliac Disease on a Gluten-free Diet

Abstract

Background: A major deficit in understanding and improving treatment in coeliac disease (CD) is the lack of empiric data on real world gluten exposure.

Aims: To estimate gluten exposure on a gluten-free diet (GFD) using immunoassays for gluten immunogenic peptides (GIP) and to examine relationships among GIP detection, symptoms and suspected gluten exposures METHODS: Adults with biopsy-confirmed CD on a GFD for 24 months were recruited from a population-based inception cohort. Participants kept a diary and collected urine samples for 10 days and stools on days 4-10. 'Doggie bags' containing ¼ portions of foods consumed were saved during the first 7 days. Gluten in food, stool and urine was quantified using A1/G12 ELISA.

Results: Eighteen participants with CD (12 female; age 21-70 years) and three participants on a gluten-containing diet enrolled and completed the study. Twelve out of 18 CD participants had a median 2.1 mg gluten per exposure (range 0.2 to >80 mg). Most exposures were asymptomatic and unsuspected. There was high intra-individual variability in the interval between gluten ingestion and excretion. Participants were generally unable to identify the food.

Conclusions: Gluten exposure on a GFD is common, intermittent, and usually silent. Excretion kinetics are highly variable among individuals. The amount of gluten varied widely, but was typically in the milligram range, which was 10-100 times less than consumed by those on an unrestricted diet. These findings suggest that a strict GFD is difficult to attain, and specific exposures are difficult to detect due to variable time course of excretion.

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References
1.
Lebwohl B, Sanders D, Green P . Coeliac disease. Lancet. 2017; 391(10115):70-81. DOI: 10.1016/S0140-6736(17)31796-8. View

2.
Falcomer A, Araujo L, Farage P, Monteiro J, Nakano E, Zandonadi R . Gluten contamination in food services and industry: A systematic review. Crit Rev Food Sci Nutr. 2018; 60(3):479-493. DOI: 10.1080/10408398.2018.1541864. View

3.
Moreno M, Munoz-Suano A, Lopez-Casado M, Torres M, Sousa C, Cebolla A . Selective capture of most celiac immunogenic peptides from hydrolyzed gluten proteins. Food Chem. 2016; 205:36-42. DOI: 10.1016/j.foodchem.2016.02.066. View

4.
Atsawarungruangkit A, Silvester J, Weiten D, Green K, Wilkey K, Rigaux L . Development of the Dietitian Integrated Evaluation Tool for Gluten-free Diets (DIET-GFD). Nutrition. 2020; 78:110819. PMC: 7502431. DOI: 10.1016/j.nut.2020.110819. View

5.
Leffler D, Dennis M, Edwards George J, Jamma S, Magge S, Cook E . A simple validated gluten-free diet adherence survey for adults with celiac disease. Clin Gastroenterol Hepatol. 2009; 7(5):530-6, 536.e1-2. DOI: 10.1016/j.cgh.2008.12.032. View