Literature DB >> 9211204

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

J B Ubbink1.   

Abstract

The relation between vitamin nutritional status and circulating plasma homocyst(e)ine concentrations is reviewed. Several studies have shown that plasma concentrations of folate, vitamin B12 and pyridoxal 5'-phosphate are inversely associated with plasma total homocyst(e)ine concentrations. Of the three vitamins mentioned above, folate is the most powerful homocyst(e)ine lowering agent and a daily supplement of 0.65 mg/day is sufficient to normalize moderate hyperhomocyst(e)inaemia in most individuals with normal renal function. In patients with severe renal failure, high doses of folate are required to treat hyperhomocyst(e)inaemia. Folic acid is ineffective in reducing plasma total homocyst(e)ine concentrations in patients with a vitamin B12 deficiency. Vitamin B6 supplementation has no effect on fasting plasma total homocyst(e)ine concentrations, but attenuates the post-methionine load plasma homocyst(e)ine peak. At least one report has shown that some individuals appear to be unable to maintain plasma total homocyst(e)ine concentrations in the normal reference range by a dietary intake of folic acid only. Long-term vitamin supplementation may be indicated in these individuals. However, the clinical benefit of vitamin supplementation has not yet been demonstrated and controlled trials are urgently required.

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Year:  1997        PMID: 9211204     DOI: 10.1023/a:1005329427711

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  45 in total

Review 1.  Will an increased dietary folate intake reduce the incidence of cardiovascular disease?

Authors:  J B Ubbink; P J Becker; W J Vermaak
Journal:  Nutr Rev       Date:  1996-07       Impact factor: 7.110

2.  Effective homocysteine metabolism may protect South African blacks against coronary heart disease.

Authors:  J B Ubbink; W J Vermaak; R Delport; A van der Merwe; P J Becker; H Potgieter
Journal:  Am J Clin Nutr       Date:  1995-10       Impact factor: 7.045

3.  Effect of various regimens of vitamin B6 and folic acid on mild hyperhomocysteinaemia in vascular patients.

Authors:  D G Franken; G H Boers; H J Blom; J M Trijbels
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

Review 4.  Metabolism of sulfur-containing amino acids.

Authors:  M H Stipanuk
Journal:  Annu Rev Nutr       Date:  1986       Impact factor: 11.848

5.  Plasma homocysteine in acute myocardial infarction: homocysteine-lowering effect of folic acid.

Authors:  F Landgren; B Israelsson; A Lindgren; B Hultberg; A Andersson; L Brattström
Journal:  J Intern Med       Date:  1995-04       Impact factor: 8.989

6.  Homocysteine and coronary artery disease in French Canadian subjects: relation with vitamins B12, B6, pyridoxal phosphate, and folate.

Authors:  K Dalery; S Lussier-Cacan; J Selhub; J Davignon; Y Latour; J Genest
Journal:  Am J Cardiol       Date:  1995-06-01       Impact factor: 2.778

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.  Plasma homocyst(e)ine, folate, and vitamin B-12 concentrations and risk for early-onset coronary artery disease.

Authors:  N Pancharuniti; C A Lewis; H E Sauberlich; L L Perkins; R C Go; J O Alvarez; M Macaluso; R T Acton; R B Copeland; A L Cousins
Journal:  Am J Clin Nutr       Date:  1994-04       Impact factor: 7.045

9.  Homocysteinemia due to folate deficiency.

Authors:  S S Kang; P W Wong; M Norusis
Journal:  Metabolism       Date:  1987-05       Impact factor: 8.694

10.  A quantitative assessment of plasma homocysteine as a risk factor for vascular disease. Probable benefits of increasing folic acid intakes.

Authors:  C J Boushey; S A Beresford; G S Omenn; A G Motulsky
Journal:  JAMA       Date:  1995-10-04       Impact factor: 56.272

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Authors:  A Aparicio; P Andrés; J M Perea; A M López-Sobaler; R M Ortega
Journal:  J Nutr Health Aging       Date:  2010-10       Impact factor: 4.075

2.  The C677T mutation of the 5,10-methylenetetrahydrofolate reductase gene is a moderate risk factor for spina bifida in Italy.

Authors:  R de Franchis; A Buoninconti; C Mandato; A Pepe; M P Sperandeo; R Del Gado; V Capra; E Salvaggio; G Andria; P Mastroiacovo
Journal:  J Med Genet       Date:  1998-12       Impact factor: 6.318

  2 in total

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