Abstract

BackgroundThe role of gluten as a trigger of symptoms in non-coeliac gluten sensitivity has been questioned.AimTo demonstrate that gluten is the trigger of symptoms in a subgroup of patients fulfilling the diagnostic criteria for non-coeliac gluten sensitivity (NCGS), which presented with lymphocytic enteritis, positive celiac genetics and negative celiac serology.MethodsDouble-blind randomized clinical trial of gluten vs placebo rechallenge. Inclusion criteria: >18 years of age, HLA-DQ2/8+, negative coeliac serology and gluten-dependent lymphocytic enteritis, and GI symptoms, with clinical and histological remission at inclusion. Eighteen patients were randomised: 11 gluten (20 g/day) and 7 placebo. Clinical symptoms, quality of life (GIQLI), and presence of gamma/delta+ cells and transglutaminase deposits were evaluated.Results91% of patients had clinical relapse during gluten challenge versus 28.5% after placebo (p = 0.01). Clinical scores and GIQLI worsened after gluten but not after placebo (p<0.01). The presence of coeliac tissue markers at baseline biopsy on a gluten-free diet allowed classifying 9 out of the 18 (50%) patients as having probable ‘coeliac lite’ disease.ConclusionThis proof-of-concept study indicates that gluten is the trigger of symptoms in a subgroup of patients fulfilling the diagnostic criteria for NCGS. They were characterized by positive celiac genetics, lymphocytic enteritis, and clinical and histological remission after a gluten-free diet.Trial RegistrationClinicalTrials.gov NCT02472704

Highlights

  • Lymphocytic enteritis (LE) is defined by normal villous architecture and intraepithelial lymphocytes (IEL) >25/100 enterocytes [1]

  • To demonstrate that gluten is the trigger of symptoms in a subgroup of patients fulfilling the diagnostic criteria for non-coeliac gluten sensitivity (NCGS), which presented with lymphocytic enteritis, positive celiac genetics and negative celiac serology

  • This proof-of-concept study indicates that gluten is the trigger of symptoms in a subgroup of patients fulfilling the diagnostic criteria for NCGS

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Summary

Introduction

Lymphocytic enteritis (LE) is defined by normal villous architecture and intraepithelial lymphocytes (IEL) >25/100 enterocytes [1]. LE is secondary to coeliac disease (CoD) only in a minority of patients, since it may be a response to other inflammatory processes in the gut. Observational studies have established CoD as accounting for 10% to 43% of cases with LE and positive HLA-DQ2/8 after exhaustive diagnostic work-up [4,5,6]. These ‘minor’ forms of CoD may have similar clinical manifestations to those with villous atrophy [7]. The role of gluten as a trigger of symptoms in non-coeliac gluten sensitivity has been questioned

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