Combination of low-dose folic acid and pyridoxine for treatment of hyperhomocysteinaemia in patients with premature arterial disease and their relatives

Citation
R. Van Der Griend et al., Combination of low-dose folic acid and pyridoxine for treatment of hyperhomocysteinaemia in patients with premature arterial disease and their relatives, ATHEROSCLER, 143(1), 1999, pp. 177-183
Citations number
35
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Journal title
ATHEROSCLEROSIS
ISSN journal
00219150 → ACNP
Volume
143
Issue
1
Year of publication
1999
Pages
177 - 183
Database
ISI
SICI code
0021-9150(199903)143:1<177:COLFAA>2.0.ZU;2-F
Abstract
Hyperhomocysteinaemia is an independent risk factor for atherosclerotic dis ease and venous thrombosis. The optimal homocysteine-lowering vitamin dose and target total homocysteine (tHcy) concentration are currently unknown. W e prospectively studied the homocysteine-lowering effect after 8 weeks low- dose combination of folic acid (0.5 mg) and pyridoxine (100 mg) in 49 hyper homocysteinaemic persons (33 patients with documented premature arterial di sease and 16 of their first-degree relatives). Hyperhomocysteinaemia was in both sexes defined as fasting tHcy concentration > 12 mu mol/l and/or post -methionine load tHcy concentration > 38 mu mol/l. Low-dose Vitamin therapy significantly reduced fasting tHcy concentration (median 13.9 to 9.3 mu mo l/l, reduction 32% (95% CI: 27-37%)) and post-load tHcy concentration (medi an 55.2 to 36.5 mu mol/l, reduction 30% (95% CI: 25-35%)). Fasting tHcy red uction was similar in women and men, as well as in patients and relatives. Post-load tHcy reduction was significantly less in men compared to women (P = 0.04) and in relatives compared to patients (P = 0.03). Although low-dos e combination of folic acid and pyridoxine results in a substantial reducti on of tHcy concentrations (30-32%) in subjects with hyperhomocysteinaemia, the normalisation percentage to predefined criteria was less impressive (49 %). (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.