Plasma homocysteine in venous thromboembolism

Haemostasis. 1991;21(1):51-7. doi: 10.1159/000216202.

Abstract

Severe hyperhomocysteinemia due to inborn errors of methionine metabolism results in precocious development of arteriosclerosis and predisposition to venous and arterial thromboembolism. Although the findings of several studies have indicated that mild hyperhomocysteinemia is common in occlusive arterial disease, no similar studies have been made on venous thromboembolism. In this study of subjects under 50 years of age, we found no significant differences in the plasma homocysteine concentrations, either in the fasting state or after methionine loading, between 42 patients with venous thromboembolism and 42 healthy controls. Nonetheless, male patients manifested a tendency toward higher homocysteine concentrations than male controls; 6 patients (14%) versus 2 controls (5%) responded abnormally to methionine loading which might indicate heterozygosity for cystathionine synthase deficiency. Thus, further studies on plasma homocysteine in venous thromboembolism are warranted.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Creatinine / blood
  • Cystathionine beta-Synthase / deficiency
  • Cystathionine beta-Synthase / genetics
  • Fasting
  • Female
  • Folic Acid / blood
  • Genetic Carrier Screening
  • Genotype
  • Homocysteine / blood*
  • Homocystinuria / complications
  • Homocystinuria / genetics
  • Humans
  • Male
  • Methionine
  • Thromboembolism / blood*
  • Thromboembolism / etiology
  • Vitamin B 12 / blood

Substances

  • Homocysteine
  • Folic Acid
  • Methionine
  • Creatinine
  • Cystathionine beta-Synthase
  • Vitamin B 12