Hyperhomocysteinemia and arteriovenous fistula thrombosis in hemodialysis patients

Am J Kidney Dis. 2005 Apr;45(4):702-7. doi: 10.1053/j.ajkd.2005.01.004.

Abstract

Background: To date, the relationship between vascular access (VA) failure and plasma total homocysteine level has been investigated only in mixed dialysis populations (ie, patients with a native arteriovenous [AV] fistula or arterial graft), whereas almost no data exist for hemodialysis patients with a native AV fistula.

Methods: In this prospective cohort study, we examined the relationship between plasma total homocysteine level and the methylenetetrahydrofolate reductase (MTHFR) gene and VA-related incident morbidity in a cohort of 205 hemodialysis patients, all with a native AV fistula.

Results: During follow-up, 78 patients experienced 1 or more VA thrombotic episodes. Patients with incident VA thrombosis had a significantly greater plasma total homocysteine level compared with patients without this event (P = 0.046). In Kaplan-Meier survival analysis, the hazard ratio for VA thrombosis increased in parallel with homocysteine level, such that patients in the third homocysteine level tertile had a relative risk for this outcome 1.72 times (95% CI, 1.21 to 2.24) greater than in those in the first tertile (log-rank test, 6.81; P = 0.009). In a multiple Cox regression model, plasma total homocysteine level was confirmed to be an independent predictor of AV fistula outcome. Plasma total homocysteine level was significantly greater (P < 0.001) in patients with the TT genotype of the MTHFR gene than in those with the CT or CC genotype.

Conclusion: VA thrombosis in dialysis patients is associated with hyperhomocysteinemia. Intervention studies are needed to clarify whether decreasing plasma homocysteine concentrations may prevent VA failure in hemodialysis patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Amino Acid Substitution
  • Arteriovenous Shunt, Surgical / adverse effects*
  • Cohort Studies
  • Comorbidity
  • Diabetic Nephropathies / complications
  • Diabetic Nephropathies / therapy
  • Disease Susceptibility
  • Female
  • Follow-Up Studies
  • Genotype
  • Humans
  • Hyperhomocysteinemia / complications*
  • Hyperhomocysteinemia / enzymology
  • Hyperhomocysteinemia / genetics
  • Incidence
  • Kidney Failure, Chronic / complications
  • Kidney Failure, Chronic / therapy
  • Life Tables
  • Male
  • Methylenetetrahydrofolate Reductase (NADPH2) / genetics
  • Middle Aged
  • Mutation, Missense
  • Point Mutation
  • Prospective Studies
  • Recurrence
  • Renal Dialysis*
  • Risk
  • Thrombophilia / enzymology
  • Thrombophilia / etiology*
  • Thrombophilia / genetics
  • Thrombosis / epidemiology*
  • Thrombosis / etiology

Substances

  • Methylenetetrahydrofolate Reductase (NADPH2)