Celiac sprue, hyperhomocysteinemia, and MTHFR gene variants

J Clin Gastroenterol. 2006 Aug;40(7):596-601. doi: 10.1097/00004836-200608000-00007.

Abstract

Goals: To describe the association of untreated celiac disease with hyperhomocysteinemia and variants of the methylenetetrahydrofolicacid reductase (MTHFR) gene found in clinical practice.

Study: Case studies with description of associated clinical, biochemical, and genetic findings and review of literature.

Results: Five new cases and 7 additional cases found from literature search of hyperhomocysteinemia with celiac sprue are reported. Treatment with gluten-free diet and folic acid led to the variable improvement in homocysteine levels. MTHFR gene variants were present in the each of the new patients described.

Conclusions: Untreated celiac disease may be associated with hyperhomocysteinemia caused by a combination of vitamin deficiencies and variants in the MTHFR gene. Abnormalities do not consistently improve with gluten-free diet. The abnormal findings could result from vitamin deficiencies or variant MTHFR status. Possible clinical implications for patients with celiac disease and hyperhomocysteinemia are reviewed.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Celiac Disease / blood
  • Celiac Disease / epidemiology
  • Celiac Disease / genetics*
  • Celiac Disease / pathology
  • Comorbidity
  • Duodenum / pathology
  • Female
  • Humans
  • Hyperhomocysteinemia / epidemiology
  • Hyperhomocysteinemia / genetics*
  • Hyperhomocysteinemia / pathology
  • Male
  • Methylenetetrahydrofolate Reductase (NADPH2) / genetics*
  • Middle Aged
  • Mutation

Substances

  • Methylenetetrahydrofolate Reductase (NADPH2)