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NDT Advance Access originally published online on November 14, 2007
Nephrology Dialysis Transplantation 2008 23(2):645-653; doi:10.1093/ndt/gfm485
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© The Author [2007]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org



Homocysteine lowering with folic acid and B vitamins in people with chronic kidney disease—results of the renal Hope-2 study{dagger}

Johannes F. E. Mann, Patrick Sheridan, Matthew J. McQueen, Claes Held, J. Malcolm O. Arnold, George Fodor, Salim Yusuf, Eva M. Lonn on behalf of the HOPE-2 investigators

Department of Medicine, Munich General Hospitals and KfH Kidney Centre, Munich Germany and Department of Medicine, McMaster University, Hamilton, Ontario, Canada

Correspondence to: J. F. E. Mann, MD, Professor of Medicine, Department of Nephrology & Hypertension, Schwabing General Hospital, Kolner Platz 1, Munchen 80804 Germany. Email: johannes.mann{at}kms.mhn.de



  Abstract

Background. Elevated plasma homocysteine levels are reported to be associated with higher rates of vascular diseases. Plasma homocysteine increases in chronic kidney disease (CKD) and could contribute to the increased cardiovascular risk in CKD.

Methods. Participants aged 55 years or older with CKD, defined as estimated GFR<60 ml/min and at high cardiovascular risk, were randomly assigned to the combination of folic acid, 2.5 mg, vitamin B6, 50 mg and vitamin B12, 1 mg (n = 307) or placebo (n = 312) daily for 5 years. The primary outcome was a composite of death from cardiovascular causes, myocardial infarction and stroke.

Results. Mean baseline plasma homocysteine was 15.9 ± 7.3 µmol/l in the active treatment group and 15.7 ± 5.7 µmol/l in placebo group and decreased to 11.9 ± 3.3 µmol/l (P < 0.001) on active treatment (15.5 ± 4.5 on placebo). Primary outcome events occurred in 90 participants (29.3%) on active therapy and in 80 (25.6%) on placebo (relative risk, 1.19; 95% confidence interval, 0.88–1.61; P = 0.25). There were no significant treatment benefits on death from cardiovascular causes (1.24; 0.84–1.83), myocardial infarction (1.10; 0.76–1.61) and stroke (1.00; 0.54–1.85). More participants in the active treatment group were hospitalized for heart failure (1.98; 1.21–3.26; P = 0.007) and for unstable angina (1.70; 1.02–2.83; P = 0.04). Incidence of primary outcome increased with decreasing GFR.

Conclusions. Active treatment with B vitamins lowered homocysteine levels in participants with CKD but did not reduce cardiovascular risk.

Keywords: clinical trial; homocysteine; myocardial infarction; stroke


{dagger}A full listing of the HOPE-2 Investigators has been published previously (reference 29)

Received for publication: 8. 3.07
Accepted in revised form: 26. 6.07


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