Prospective Study of Hyperhomocysteinemia as an Adverse Cardiovascular Risk Factor in End-Stage Renal Disease

Author:

Moustapha Ali1,Naso Arabi1,Nahlawi Maher1,Gupta Anjan1,Arheart Kristopher L.1,Jacobsen Donald W.1,Robinson Killian1,Dennis Vincent W.1

Affiliation:

1. From the Departments of Internal Medicine (A.M., A.N., M.N., A.G.), Biostatistics and Epidemiology (K.A.), Cell Biology (D.W.J.), Cardiology (K.R.), and Nephrology and Hypertension (V.W.D.), The Cleveland Clinic Foundation, Cleveland, Ohio. Dr Gupta is currently at the Department of Cardiology, Sinai Samaritan Medical Center, Milwaukee, Wis.

Abstract

Background —Retrospective and case-control studies show that hyperhomocysteinemia is an independent risk factor for atherosclerosis in patients with end-stage renal disease. We studied prospectively the association between total homocysteine and cardiovascular outcomes. Methods and Results —In all, 167 patients (93 men, 74 women; mean age, 56.3±14.7 years) were followed for a mean duration of 17.4±6.4 months. Cardiovascular events and causes of mortality were related to total homocysteine values and other cardiovascular risk factors. Cox regression analysis was used to identify the independent predictors for cardiovascular events and mortality. Fifty-five patients (33%) developed cardiovascular events and 31 (19%) died, 12 (8%) of cardiovascular causes. Total plasma homocysteine values ranged between 7.9 and 315.0 μmol/L. Levels were higher in patients who had cardiovascular events or died of cardiovascular causes (43.0±48.6 versus 26.9±14.9 μmol/L, P =.02). The relative risk (RR) for cardiovascular events, including death, increased 1% per μmol/L increase in total homocysteine concentration (RR, 1.01; CI, 1.00 to 1.01; P =.01). Conclusions —These prospective observations confirm that hyperhomocysteinemia is an independent risk factor for cardiovascular morbidity and mortality in end-stage renal disease, with an increased RR of 1% per μmol/L increase in total homocysteine concentration. Interventional studies are needed to evaluate the possible effects of modifying this risk factor in these patients.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference19 articles.

1. US Renal Data System USRDS. Annual Data Report; National Institutes of Health National Institute of Diabetes and Digestive and Kidney Diseases Bethesda Md April 1996 1996.

2. Chauveau P Chadefaux B Coude M Aupetit J Hannedouche T Kamoun P Jungers P. Hyperhomocysteinaemia a risk factor for atherosclerosis in chronic uremic patients. Kidney Int . 1993;43(suppl 41):S72–S77.

3. Hyperhomocysteinemia and the risk for vascular disease in hemodialysis patients.

4. Rapid HPLC determination of total homocysteine and other thiols in serum and plasma: sex differences and correlation with cobalamin and folate concentrations in healthy subjects

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