Cardiovascular actions of mineralocorticoid receptor antagonists in patients with chronic kidney disease: A systematic review and meta-analysis of randomized trials

被引:12
作者
Ng, Khai P. [1 ,2 ]
Arnold, Julia [1 ,2 ]
Sharif, Adnan [1 ,2 ]
Gill, Paramjit [3 ]
Townend, Jonathan N. [2 ,4 ]
Ferro, Charles J. [1 ,2 ]
机构
[1] Queen Elizabeth Hosp, Dept Nephrol, Birmingham B15 2WB, W Midlands, England
[2] Univ Birmingham, Birmingham B15 2TT, W Midlands, England
[3] Univ Birmingham, Primary Care Clin Sci, Birmingham B15 2TT, W Midlands, England
[4] Queen Elizabeth Hosp, Dept Cardiol, Birmingham, W Midlands, England
基金
美国国家卫生研究院;
关键词
Mineralocorticoid receptor antagonists; chronic kidney disease; cardiovascular actions; aldosterone; safety; meta-analysis; systematic review; ANGIOTENSIN-ALDOSTERONE SYSTEM; CONVERTING ENZYME-INHIBITOR; DOUBLE-BLIND; DIABETIC-NEPHROPATHY; ADDITIVE THERAPY; RENAL-DISEASE; SPIRONOLACTONE; BLOCKADE; ALBUMINURIA; SAFETY;
D O I
10.1177/1470320315575849
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Introduction: The safety and actions of mineralocorticoid receptor antagonists on surrogate markers of cardiovascular disease as well as major patient level cardiovascular end-points in patients with chronic kidney disease are unclear. Methods: MEDLINE, EMBASE, Trip Database, Cochrane Central Register of Controlled Trials, Cochrane Renal Group specialized register, Current Controlled Trials and clinicaltrials.gov were searched for relevant trials. Results: Twenty-nine trials (1581 patients) were included. Overall, mineralocorticoid receptor antagonists lowered both systolic and diastolic blood pressure (-5.24, 95% confidence interval (CI) -8.65, -1.82 mmHg; p=0.003 and -1.96, 95% CI -3.22, -0.69 mmHg; p=0.002 respectively). There were insufficient data to perform a meta-analysis of other cardiovascular effects. However, a systematic review of the studies included suggested a consistent improvement in surrogate markers of cardiovascular disease. Overall, the use of mineralocorticoid receptor antagonists was associated with an increased serum potassium (0.23, 95% CI 0.13, 0.33 mmol/l; p<0.0001) and higher risk ratio (1.76, 95% CI 1.20, 2.57; p=0.001) of hyperkalemia. Data on long-term cardiovascular outcomes and mortality were not available in any of the trials. Conclusions: The long-term effects of mineralocorticoid receptor antagonists on cardiovascular events, mortality and safety need to be established.
引用
收藏
页码:599 / 613
页数:15
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