Is a gluten-free diet necessary in Marsh I intestinal lesions in patients with HLADQ2, DQ8 genotype and without gastrointestinal symptoms?

Curr Opin Clin Nutr Metab Care. 2012 Sep;15(5):505-10. doi: 10.1097/MCO.0b013e3283566643.

Abstract

Purpose of review: To describe whether a gluten-free diet (GFD) is indicated in Marsh I gluten-sensitive enteropathy where gastrointestinal symptoms are not present. Arguments are provided to prescribe a GFD to manage extraintestinal symptoms. By contrast, there are not enough reasons to prescribe a GFD to prevent long-term complications.

Recent findings: Population-based and prospective observational studies have found that lymphocytic duodenosis may be due to not just gluten-sensitive enteropathy but also due to other aetiologic factors. Marsh I type lesions may be the cause of iron-deficiency anaemia of unknown aetiology which is reverted by a GFD. A similar effect seems to occur with bone mineralization and hypertransaminasemia. The beneficial influence of a GFD reducing lymphoma and coeliac disease-related mortality remains controversial.

Summary: An appropriate differential diagnosis of the lymphocytic duodenosis is essential before a GFD is indicated. As a third of patients remained undiagnosed, in spite of genetic study and specific coeliac serology, flow cytometry and transglutaminase antibodies in duodenal tissue may be helpful in establishing gluten-sensitive enteropathy diagnosis. Future studies should assess whether lymphoma risk is reduced by a GFD in Marsh I patients. Also a more precise benefit in bone mineralization in this setting is needed.

Publication types

  • Review

MeSH terms

  • Anemia, Iron-Deficiency / etiology
  • Antibodies / metabolism
  • Bone Density
  • Celiac Disease / diet therapy*
  • Celiac Disease / genetics
  • Celiac Disease / pathology
  • Diagnosis, Differential
  • Diet, Gluten-Free*
  • Duodenal Diseases / diet therapy*
  • Duodenal Diseases / genetics
  • Duodenal Diseases / pathology
  • Duodenum / immunology
  • Duodenum / pathology*
  • Genotype
  • HLA-DQ Antigens / genetics
  • Humans
  • Lymphocytes / pathology*
  • Lymphoma / prevention & control
  • Transglutaminases / immunology*

Substances

  • Antibodies
  • HLA-DQ Antigens
  • Transglutaminases