No effect of B vitamins on ADMA levels in patients at increased cardiovascular risk

Clin Endocrinol (Oxf). 2006 May;64(5):495-501. doi: 10.1111/j.1365-2265.2006.02497.x.

Abstract

Objective: Asymmetric dimethylarginine (ADMA) is a recently identified potent cardiovascular risk factor. ADMA levels are increased in hyperhomocysteinaemia and the metabolism of ADMA is linked with that of homocysteine in several ways. Treatment with B vitamins effectively reduces homocysteine levels, but studies investigating the effect on ADMA levels are scarce and show conflicting results. In this study we evaluated the effect of treatment with B vitamins on ADMA levels in two high cardiovascular risk populations.

Methods: In study I, 110 siblings of patients with clinical atherosclerotic disease and postmethionine hyperhomocysteinaemia were treated with 5 mg of folic acid and 250 mg of pyridoxine or placebo, and were analysed after 1 year. In study II, 41 patients with type 2 diabetes and mild hyperhomocysteinaemia were analysed after 6 months treatment with 5 mg of folic acid or placebo.

Results: A correlation between baseline homocysteine and ADMA levels was found, which was partly due to confounding by renal function. Homocysteine levels decreased by 43% in study I and by 28% in study II. In both studies, treatment with B vitamins had no effect at all on ADMA, arginine/ADMA ratio and SDMA levels. This result was confirmed in multiple linear regression analyses with adjustment for baseline values and gender.

Conclusions: Our studies indicate that B vitamins, despite causing a substantial reduction in plasma homocysteine levels, have no beneficial effect on ADMA levels.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Adolescent
  • Adult
  • Arginine / analogs & derivatives*
  • Arginine / blood
  • Atherosclerosis / blood
  • Atherosclerosis / drug therapy
  • Cardiovascular Diseases / blood
  • Cardiovascular Diseases / prevention & control*
  • Diabetes Mellitus, Type 2 / blood
  • Diabetes Mellitus, Type 2 / drug therapy
  • Double-Blind Method
  • Drug Administration Schedule
  • Female
  • Folic Acid / therapeutic use*
  • Humans
  • Hyperhomocysteinemia / blood
  • Hyperhomocysteinemia / drug therapy*
  • Linear Models
  • Male
  • Middle Aged
  • Pyridoxine / therapeutic use*
  • Risk Factors
  • Time Factors
  • Treatment Failure
  • Vitamin B Complex / therapeutic use*

Substances

  • dimethylarginine
  • Vitamin B Complex
  • N,N-dimethylarginine
  • Folic Acid
  • Arginine
  • Pyridoxine