Tailoring mineralocorticoid receptor antagonist therapy in heart failure patients: are we moving towards a personalized approach?

被引:28
作者
Ferreira, Joao Pedro [1 ,2 ]
Mentz, Robert J. [3 ,4 ]
Pizard, Anne [1 ]
Pitt, Bertram [5 ]
Zannad, Faiez [1 ]
机构
[1] Univ Lorraine, Ctr Invest Clin Plurithemat 1433, INSERM U1116, Nancy, France
[2] Univ Porto, Dept Physiol & Cardiothorac Surg, Cardiovasc Res & Dev Unit, Fac Med, Oporto, Portugal
[3] Duke Univ, Med Ctr, Duke Clin Res Inst, Durham, NC USA
[4] Duke Univ, Med Ctr, Div Cardiol, Dept Med, Durham, NC USA
[5] Univ Michigan, Sch Med, Dept Cardiol, Ann Arbor, MI USA
关键词
Personalized medicine; Mineralocorticoid receptor antagonists; Heart failure; PRESERVED EJECTION FRACTION; MILD PATIENTS HOSPITALIZATION; WORSENING RENAL-FUNCTION; SODIUM ZIRCONIUM CYCLOSILICATE; ACUTE MYOCARDIAL-INFARCTION; EMPHASIS-HF; PROGNOSTIC IMPORTANCE; CLINICAL BENEFITS; AFRICAN-AMERICANS; CARDIAC STRUCTURE;
D O I
10.1002/ejhf.814
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aim of personalized medicine is to offer a tailored approach to each patient in order to provide the most effective therapy, while reducing risks and side effects. The use of mineralocorticoid receptor antagonists (MRAs) has demonstrated major benefits in heart failure with reduced ejection fraction (HFrEF), results with challenging inconsistencies in heart failure with preserved ejection fraction (HFpEF), and 'neutral' preliminary results in acute heart failure. Data derived from landmark trials are generally applied in a 'one size fits all' manner and the development and implementation of more personalized MRA management would offer the potential to improve outcomes and reduce side effects. However, the personalization of pharmacotherapy regimens remains poorly defined in the cardiovascular field (in light of current knowledge) and until further trials targeting specific subpopulations have been conducted, MRAs should be provided to the great majority of HFrEF patients in the absence of contraindication. Spironolactone should be considered for symptomatic HFpEF patients with elevated natriuretic peptides. In the near future, trials should target HFrEF patients using exclusion criteria sourced from landmark trials (e.g. severe renal impairment), select more homogeneous HFpEF populations (e.g. with elevated BNP and structural abnormalities on echocardiography), and determine which patients are likely to benefit from MRAs (e.g. according to prespecified biomarkers).
引用
收藏
页码:974 / 986
页数:13
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