Literature DB >> 8123653

Treatment of mild hyperhomocysteinemia in vascular disease patients.

D G Franken1, G H Boers, H J Blom, F J Trijbels, P W Kloppenborg.   

Abstract

Mild hyperhomocysteinemia is recognized as a risk factor for premature arteriosclerotic disease. A few vitamins and other substances have been reported to reduce blood homocysteine levels, but normalization of elevated blood homocysteine concentrations with any of these substances has not been reported. Therefore, we screened 421 patients suffering from premature peripheral or cerebral occlusive arterial disease by oral methionine loading tests for the presence of mild hyperhomocysteinemia. Thirty-three percent of patients with peripheral and 20% of patients with cerebral occlusive arterial disease were identified with mild hyperhomocysteinemia (14% of the men, 34% of the premenopausal women, and 26% of the postmenopausal women). Mildly hyperhomocysteinemic patients were administered vitamin B6 250 mg daily. After 6 weeks methionine loading tests were again assessed to evaluate the effect of treatment. Patients with nonnormalized homocysteine concentrations were further treated with vitamin B6 250 mg daily and/or folic acid 5 mg daily and/or betaine 6 g daily, solely or in any combination. Vitamin B6 treatment normalized the afterload homocysteine concentration in 56% of the treated patients (71% of the men, 45% of the premenopausal women, and 88% of the postmenopausal women). Further treatment resulted in a normalization of homocysteine levels in 95% of the remaining cases. Thus, mild hyperhomocysteinemia, which is frequently encountered in patients with premature arteriosclerotic disease, can be reduced to normal in virtually all cases by safe and simple treatment with vitamin B6, folic acid, and betaine, each of which is involved in methionine metabolism.

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Year:  1994        PMID: 8123653     DOI: 10.1161/01.atv.14.3.465

Source DB:  PubMed          Journal:  Arterioscler Thromb        ISSN: 1049-8834


  23 in total

1.  Determinants and vitamin responsiveness of intermediate hyperhomocysteinemia (> or = 40 micromol/liter). The Hordaland Homocysteine Study.

Authors:  A B Guttormsen; P M Ueland; I Nesthus; O Nygård; J Schneede; S E Vollset; H Refsum
Journal:  J Clin Invest       Date:  1996-11-01       Impact factor: 14.808

2.  [A young patient with multiple arterial occlusions].

Authors:  C Panzere; A Brieke; B Bräuer; F Eggemann; H M Becker; P Dieterle
Journal:  Med Klin (Munich)       Date:  1998-05-15

3.  A cost-benefit analysis of a cardiovascular disease prevention trial, using folate supplementation as an example.

Authors:  J Hornberger
Journal:  Am J Public Health       Date:  1998-01       Impact factor: 9.308

Review 4.  Assessment of homocysteine status.

Authors:  H Refsum; T Fiskerstrand; A B Guttormsen; P M Ueland
Journal:  J Inherit Metab Dis       Date:  1997-06       Impact factor: 4.982

5.  Lowering blood homocysteine with folic acid based supplements: meta-analysis of randomised trials. Homocysteine Lowering Trialists' Collaboration.

Authors: 
Journal:  BMJ       Date:  1998-03-21

Review 6.  The role of vitamins in the pathogenesis and treatment of hyperhomocyst(e)inaemia.

Authors:  J B Ubbink
Journal:  J Inherit Metab Dis       Date:  1997-06       Impact factor: 4.982

Review 7.  Hyperhomocysteinaemia; with reference to its neuroradiological aspects.

Authors:  M van den Berg; M S van der Knaap; G H Boers; C D Stehouwer; J A Rauwerda; J Valk
Journal:  Neuroradiology       Date:  1995-07       Impact factor: 2.804

Review 8.  New approaches to the prevention of atherosclerosis.

Authors:  M Naito; T Hayashi; A Iguchi
Journal:  Drugs       Date:  1995-09       Impact factor: 9.546

Review 9.  Homocysteine levels in patients with stroke: clinical relevance and therapeutic implications.

Authors:  G J Hankey; J W Eikelboom
Journal:  CNS Drugs       Date:  2001       Impact factor: 5.749

10.  Does the polymorphism 677C-T of the 5,10-methylenetetrahydrofolate reductase gene contribute to homocysteine-related vascular disease?

Authors:  L Thuillier; B Chadefaux-Vekemans; J P Bonnefont; A Kara; J Aupetit; C Rochette; G Montalescot; M C Couty; P Kamoun; A Ankri
Journal:  J Inherit Metab Dis       Date:  1998-12       Impact factor: 4.982

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