Literature DB >> 8949585

Homocystinuria: what about mild hyperhomocysteinaemia?

M van den Berg1, G H Boers.   

Abstract

Hyperhomocysteinaemia is associated with an increased risk of atherosclerotic vascular disease and thromboembolism, in both men and women. A variety of conditions can lead to elevated homocysteine levels, but the relation between high levels and vascular disease is present regardless of the underlying cause. Pooled data from a large number of studies demonstrate that mild hyperhomocysteinaemia after a standard methionine load is present in 21% of young patients with coronary artery disease, in 24% of patients with cerebrovascular disease, and in 32% of patients with peripheral vascular disease. From such data an odds ratio of 13.0 (95% confidence interval 5.9 to 28.1), as an estimate of the relative risk of vascular disease at a young age, can be calculated in subjects with an abnormal response to methionine loading. Furthermore, mild hyperhomo-cysteinaemia can lead to a two- or three-fold increase in the risk of recurrent venous thrombosis. Elevated homocysteine levels can be reduced to normal in virtually all cases by simple and safe treatment with vitamin B6, folic acid, and betaine, each of which is involved in methionine metabolism. A clinically beneficial effect of such an intervention, currently under investigation, would make large-scale screening for this risk factor mandatory.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8949585      PMCID: PMC2398569          DOI: 10.1136/pgmj.72.851.513

Source DB:  PubMed          Journal:  Postgrad Med J        ISSN: 0032-5473            Impact factor:   2.401


  39 in total

Review 1.  Plasma homocysteine, a risk factor for vascular disease: plasma levels in health, disease, and drug therapy.

Authors:  P M Ueland; H Refsum
Journal:  J Lab Clin Med       Date:  1989-11

Review 2.  Impaired homocysteine metabolism in early-onset cerebral and peripheral occlusive arterial disease. Effects of pyridoxine and folic acid treatment.

Authors:  L Brattström; B Israelsson; B Norrving; D Bergqvist; J Thörne; B Hultberg; A Hamfelt
Journal:  Atherosclerosis       Date:  1990-02       Impact factor: 5.162

3.  Hyperhomocysteinemia: an independent risk factor for vascular disease.

Authors:  R Clarke; L Daly; K Robinson; E Naughten; S Cahalane; B Fowler; I Graham
Journal:  N Engl J Med       Date:  1991-04-25       Impact factor: 91.245

Review 4.  Clinical significance of pharmacological modulation of homocysteine metabolism.

Authors:  H Refsum; P M Ueland
Journal:  Trends Pharmacol Sci       Date:  1990-10       Impact factor: 14.819

5.  Improved identification of heterozygotes for homocystinuria due to cystathionine synthase deficiency by the combination of methionine loading and enzyme determination in cultured fibroblasts.

Authors:  G H Boers; B Fowler; A G Smals; F J Trijbels; A I Leermakers; W J Kleijer; P W Kloppenborg
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

6.  Endothelial cell injury due to copper-catalyzed hydrogen peroxide generation from homocysteine.

Authors:  G Starkebaum; J M Harlan
Journal:  J Clin Invest       Date:  1986-04       Impact factor: 14.808

7.  The natural history of homocystinuria due to cystathionine beta-synthase deficiency.

Authors:  S H Mudd; F Skovby; H L Levy; K D Pettigrew; B Wilcken; R E Pyeritz; G Andria; G H Boers; I L Bromberg; R Cerone
Journal:  Am J Hum Genet       Date:  1985-01       Impact factor: 11.025

8.  The association of elevated plasma homocyst(e)ine with progression of symptomatic peripheral arterial disease.

Authors:  L M Taylor; R D DeFrang; E J Harris; J M Porter
Journal:  J Vasc Surg       Date:  1991-01       Impact factor: 4.268

9.  Thermolabile methylenetetrahydrofolate reductase: an inherited risk factor for coronary artery disease.

Authors:  S S Kang; P W Wong; A Susmano; J Sora; M Norusis; N Ruggie
Journal:  Am J Hum Genet       Date:  1991-03       Impact factor: 11.025

10.  Intermediate hyperhomocysteinemia resulting from compound heterozygosity of methylenetetrahydrofolate reductase mutations.

Authors:  S S Kang; P W Wong; H G Bock; A Horwitz; A Grix
Journal:  Am J Hum Genet       Date:  1991-03       Impact factor: 11.025

View more
  3 in total

1.  Hyperhomocyst(e)inemia.

Authors: 
Journal:  Curr Treat Options Cardiovasc Med       Date:  2000-02

Review 2.  Hyperhomocysteinaemia and associated disease.

Authors:  R C Bakker; D P Brandjes
Journal:  Pharm World Sci       Date:  1997-06

3.  Hyperhomocysteinaemia.

Authors:  T O Cheng
Journal:  Postgrad Med J       Date:  1997-09       Impact factor: 2.401

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.