Antioxidant therapy in hemodialysis patients: a systematic review

被引:91
作者
Coombes, Jeff S. [2 ]
Fassett, Robert G. [1 ,2 ,3 ]
机构
[1] Royal Brisbane & Womens Hosp, Dept Renal Med, Brisbane, Qld 4029, Australia
[2] Univ Queensland, Sch Human Movement Studies, Brisbane, Qld, Australia
[3] Univ Queensland, Sch Med, Brisbane, Qld, Australia
关键词
ESRD; oxidative stress; vitamin C; VITAMIN-E SUPPLEMENTATION; STAGE RENAL-DISEASE; LOW-DENSITY-LIPOPROTEIN; RANDOMIZED-CONTROLLED-TRIAL; PLACEBO-CONTROLLED TRIAL; BLOOD MONONUCLEAR-CELLS; CHRONIC KIDNEY-DISEASE; RED GRAPE JUICE; OXIDATIVE STRESS; LIPID-PEROXIDATION;
D O I
10.1038/ki.2011.341
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Antioxidants have been used as therapies to decrease oxidative stress and improve CVD risk in hemodialysis (HD) patients. A systematic search of the Medline database (search date 30 April 2011) found 56 studies investigating the effects of antioxidant therapies on biomarkers of oxidative stress (53 studies) or clinical outcomes (3 studies). The majority were small trials using a nonrandomized open-label design with a single HD group (no HD controls). Alpha-tocopherol was the most investigated antioxidant, with 20/25 studies reporting that this vitamin decreased oxidative stress, and one clinical outcome trial in 196 patients finding that it protected against secondary CVD. Studies using vitamin C were more equivocal, with 4/11 showing decreased oxidative stress and one clinical outcome trial showing no effect on morbidity or mortality. N-acetylcysteine was the most efficacious agent, with 4/4 studies indicating a decrease in oxidative stress and one trial (n = 134) showing reduced CVD events. Seven studies have used therapy containing a combination of antioxidants, with five of these reporting decreased oxidative stress. Most intervention studies in HD patients, such as statin therapy and increased dialysis dose, have failed to show improvement in CVD outcomes. Two intervention trials using different antioxidants have found CVD benefits, suggesting that this line of therapy is effective in this resistant population. These studies require validation in larger, adequately powered trials. Kidney International (2012) 81, 233-246; doi: 10.1038/ki.2011.341; published online 5 October 2011
引用
收藏
页码:233 / 246
页数:14
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