Evolving role for mineralocorticoid receptor antagonists in heart failure with preserved ejection fraction

被引:4
|
作者
Miller, Robert J. H. [1 ]
Howlett, Jonathan G. [1 ]
机构
[1] Univ Calgary, Libin Cardiovasc Inst Alberta, Calgary, AB, Canada
关键词
heart failure; heart failure with preserved ejection fraction; mineralocorticoid receptor antagonist; spironolactone; BRAIN NATRIURETIC PEPTIDE; DIASTOLIC FUNCTION; SPIRONOLACTONE THERAPY; ATRIAL-FIBRILLATION; CARDIAC STRUCTURE; OLDER PATIENTS; ALDOSTERONE; DYSFUNCTION; PROGNOSIS; MORTALITY;
D O I
10.1097/HCO.0000000000000147
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of reviewThe majority of randomized clinical trials in heart failure with preserved ejection fraction (HFpEF) have failed to show meaningful improvements in clinical outcomes. Recent randomized trials have shown benefits from mineralocorticoid receptor antagonists (MRAs) in the management of HFpEF. This review will focus on new evidence for MRA therapy in patients with HFpEF.Recent findingsThree randomized trials were reviewed: the Effect of spironolactone on diastolic function and exercise capacity in patients with heart failure with preserved ejection fraction: the Aldo-DHF randomized controlled trial; the Treatment of Preserved Cardiac Function Heart Failure with an Aldosterone Antagonist trial; and its echocardiography substudy. The Aldo-DHF trial showed improvements in echocardiographic measures of diastolic function. In the Treatment of Preserved Cardiac Function Heart Failure With an Aldosterone Antagonist trial, hospitalization for heart failure was significantly reduced with MRA therapy with no difference in the primary outcome of cardiovascular death or hospitalization. In patients with high risk, however, there may be a reduction in cardiovascular mortality. We will also briefly discuss finerenone, a new generation MRA associated with a lower incidence of hyperkalemia.SummaryNew evidence shows that MRA therapy decreases left ventricular mass and left atrial size, reduces hospitalization, and may reduce cardiovascular mortality in patients with high risk.
引用
收藏
页码:168 / 172
页数:5
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