Gluten-free diet has a beneficial effect on chromosome instability in lymphocytes of children with coeliac disease

J Pediatr Gastroenterol Nutr. 2004 Feb;38(2):177-80. doi: 10.1097/00005176-200402000-00014.

Abstract

Objectives: Children with coeliac disease (CD) have an increased number of chromosome aberrations in peripheral blood lymphocytes. Whether genetically determined or a secondary phenomenon in CD, chromosome abnormalities may be involved in the predisposition to cancer in CD patients. The aim of the study was to follow a group of children with CD in whom the initial frequency of chromosome aberrations at diagnosis was known and to measure the same variable after a minimum of 2 years on a gluten-free diet.

Methods: Chromosome aberrations in peripheral blood lymphocytes were determined in 17 patients with CD, before and after at least 24 months of a gluten free diet (mean, 33 months), and in 15 healthy children. The differences in the frequency of aberrations were analyzed by Mann-Whitney U test and Wilcoxon matched-pairs signed-ranks test.

Results: Twelve patients adhered to the diet and had a significantly lower frequency of chromosome aberrations than did 5 patients not following the diet (0.16% v 1.2%; P = 0.03), whereas at presentation there had been no difference (1.54% v 1.2%; P = 0.09). The frequency of aberrations at follow-up in patients who were diet adherent was significantly lower than at presentation (1.54% v 0.16%; P = 0.02) and remained unchanged in patients who were not diet adherent (1.2% v 1.2%; P = 1). After at least 24 months of a gluten-free diet, children with CD did not differ from healthy control subjects (0.16% v 0.27%; P = 0.54), whereas children not following the diet had an increased frequency of aberrations (1.2% v 0.27%; P = 0.05).

Conclusions: The frequency of chromosome aberrations in peripheral blood lymphocytes of patients with CD decreased significantly on a gluten-free diet. We conclude that genomic instability is a secondary phenomenon, possibly caused by chronic intestinal inflammation.

MeSH terms

  • Adolescent
  • Case-Control Studies
  • Celiac Disease* / diet therapy
  • Celiac Disease* / genetics
  • Celiac Disease* / physiopathology
  • Cell Cycle
  • Child
  • Child, Preschool
  • Chromosome Aberrations*
  • Female
  • Follow-Up Studies
  • Glutens / administration & dosage*
  • Humans
  • Infant
  • Longitudinal Studies
  • Lymphocytes / pathology*
  • Male
  • Patient Compliance

Substances

  • Glutens