Homocysteine and Cardiovascular Disease
- 1 February 1998
- journal article
- review article
- Published by Annual Reviews in Annual Review of Medicine
- Vol. 49 (1) , 31-62
- https://doi.org/10.1146/annurev.med.49.1.31
Abstract
An elevated level of total homocysteine (tHcy) in blood, denoted hyperhomocysteinemia, is emerging as a prevalent and strong risk factor for atherosclerotic vascular disease in the coronary, cerebral, and peripheral vessels, and for arterial and venous thromboembolism. The basis for these conclusions is data from about 80 clinical and epidemiological studies including more than 10,000 patients. Elevated tHcy confers a graded risk with no threshold, is independent of but may enhance the effect of the conventional risk factors, and seems to be a particularly strong predictor of cardiovascular mortality. Hyperhomocysteinemia is attributed to commonly occurring genetic and acquired factors including deficiencies of folate and vitamin B12. Supplementation with B-vitamins, in particular with folic acid, is an efficient, safe, and inexpensive means to reduce an elevated tHcy level. Studies are now in progress to establish whether such therapy will reduce cardiovascular risk.Keywords
This publication has 247 references indexed in Scilit:
- A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductaseNature Genetics, 1995
- Homocysteine response to methionine challenge in four obligate heterozygotes for homocystinuria and relationship with cystathionine β ‐synthase mutationsJournal of Inherited Metabolic Disease, 1995
- Persistent hypermethioninaemia with dominant inheritanceJournal of Inherited Metabolic Disease, 1991
- Homocysteine, factor VII and antithrombin III in subjects with different gene dosage for cystathionine β‐synthaseJournal of Inherited Metabolic Disease, 1988
- Neuropsychiatric Disorders Caused by Cobalamin Deficiency in the Absence of Anemia or MacrocytosisNew England Journal of Medicine, 1988
- Oxidation of low-density lipoprotein by thiol compounds leads to its recognition by the acetyl LDL receptorBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1987
- Protein‐Bound Homocyst(e)ine in Patients With Rheumatoid Arthritis Undergoing D‐Penicillamine TreatmentThe Journal of Clinical Pharmacology, 1986
- Heterozygosity for Homocystinuria in Premature Peripheral and Cerebral Occlusive Arterial DiseaseNew England Journal of Medicine, 1985
- Homocystinuria associated with decreased methylenetetrahydrofolate reductase activityBiochemical and Biophysical Research Communications, 1972
- The identification of homocystine in the urineBiochemical and Biophysical Research Communications, 1962