Genetic aspects of hyperhomocysteinemia in chronic kidney disease

Semin Nephrol. 2006 Jan;26(1):8-13. doi: 10.1016/j.semnephrol.2005.06.003.

Abstract

Patients with chronic kidney disease who are on dialysis or with a kidney transplant have higher total plasma homocysteine concentrations than individuals who are free from kidney disease. Several single-nucleotide polymorphisms of genes encoding enzymes that are involved in homocysteine metabolism have been studied in these patients. These polymorphisms are located in genes encoding of 5,10-methylenetetrahydrofolate reductase (MTHFR), methionine synthase reductase, methionine synthase, cystathionine beta-synthase, glutamate carboxy peptidase II, reduced folate carrier 1, and transcobalamin II. Among the single-nucleotide polymorphisms studied, only MTHFR 677C>T was associated consistently with total plasma homocysteine levels, but there currently is no evidence of any association between MTHFR 677C>T genotype and long-term outcomes.

Publication types

  • Review

MeSH terms

  • Chronic Disease
  • Humans
  • Hyperhomocysteinemia / etiology*
  • Hyperhomocysteinemia / genetics*
  • Kidney Diseases / complications*
  • Methylenetetrahydrofolate Reductase (NADPH2) / genetics
  • Polymorphism, Genetic

Substances

  • Methylenetetrahydrofolate Reductase (NADPH2)