Secondary prevention with antioxidants of cardiovascular disease in endstage renal disease (SPACE): randomised placebo-controlled trial

被引:807
作者
Boaz, M [1 ]
Smetana, S
Weinstein, T
Matas, Z
Gafter, U
Iaina, A
Knecht, A
Weissgarten, Y
Brunner, D
Fainaru, M
Green, MS
机构
[1] E Wolfson Med Ctr, Inst Nephrol, IL-58100 Holon, Israel
[2] Tel Aviv Univ, Sackler Fac Med, Dept Epidemiol & Prevent Med, IL-69978 Tel Aviv, Israel
[3] E Wolfson Med Ctr, Biochem Lab, IL-58100 Holon, Israel
[4] E Wolfson Med Ctr, Inst Physiol Hyg, IL-58100 Holon, Israel
[5] Tel Aviv Univ, Sackler Fac Med, Rabin Med Ctr, Lipid Res Lab, IL-69978 Tel Aviv, Israel
[6] Israel Ctr Dis Control, Tel Hashomer, Israel
[7] Rabin Med Ctr, Dept Nephrol, Petah Tiqwa, Israel
[8] Ichilov Med Ctr, Dept Nephrol, Tel Aviv, Israel
[9] Chaim Sheba Med Ctr, Dept Nephrol, IL-52621 Tel Hashomer, Israel
[10] Asaf Harofeh Med Ctr, Dept Nephrol, Zrifin, Israel
关键词
D O I
10.1016/S0140-6736(00)02783-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Excess cardiovascular mortality has been documented in chronic haemodialysis patients. Oxidative stress is greater in haemodialysis patients with prevalent cardiovascular disease than in those without, suggesting a role for oxidative stress in excess cardiovascular disease in haemodialysis. We investigated the effect of high-dose vitamin E supplementation on cardiovascular disease outcomes in haemodialysis patients with pre-existing cardiovascular disease. Methods Haemodialysis patients with pre-existing cardiovascular disease (n=196) aged 40-75 years at baseline from six dialysis centres were enrolled and randomised to receive 800 IU/day vitamin E or matching placebo. Patients were followed for a median 519 days. The primary endpoint was a composite variable consisting of: myocardial infarction (fatal and non-fatal), ischaemic stroke, peripheral vascular disease (excluding the arteriovenous fistula), and unstable angina. Secondary outcomes included each of the component outcomes, total mortality, and cardiovascular-disease mortality. Findings A total of 15 (16%) of the 97 patients assigned to vitamin E and 33 (33%) of the 99 patients assigned to placebo had a primary endpoint (relative risk 0.46 [95% CI 0.27-0.78], p=0.014). Five (5.1%) patients assigned to vitamin E and 17 (17.2%) patients assigned to placebo had myocardial infarction (0.3 [0.11-0.78], p=0.016). No significant differences in other secondary endpoints, cardiovascular disease, or total mortality were detected. Interpretation In haemodialysis patients with prevalent cardiovascular disease, supplementation with 800 IU/day vitamin E reduces composite cardiovascular diesease endpoints and myocardial infarction.
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收藏
页码:1213 / 1218
页数:6
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