Strategies to attenuate pathological remodeling in heart failure

被引:11
作者
Eapen, Zubin
Rogers, Joseph G. [1 ,2 ]
机构
[1] Duke Univ, Med Ctr, Div Cardiol, Dept Med, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Duke Clin Res Inst, Durham, NC 27710 USA
关键词
cardiac resynchronization therapy; cardiac support device; heart failure; ventricular remodeling; LEFT-VENTRICULAR DYSFUNCTION; ACUTE MYOCARDIAL-INFARCTION; DOPPLER-ECHOCARDIOGRAPHIC EVIDENCE; CARDIAC RESYNCHRONIZATION THERAPY; RANDOMIZED INTERVENTION TRIAL; CONVERTING-ENZYME-INHIBITORS; LONG-TERM PROGRESSION; ACORN CLINICAL-TRIAL; SYSTOLIC DYSFUNCTION; ANGIOTENSIN-II;
D O I
10.1097/HCO.0b013e32832a11ff
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review The incidence of heart failure is increasing due to an aging population and improved management of diseases that are precursors to ventricular dysfunction. The success of therapeutic advances has created a challenge for the next generation of investigational heart failure treatments because the mortality rate has decreased to such a degree that larger trials will be needed to demonstrate mortality advantage. Prior work has linked favorable changes in ventricular geometry to improved survival, suggesting that remodeling may be a suitable surrogate endpoint. Recent findings In addition to the established benefits of neurohormonal blockade, new mechanical and electrical therapies are proving beneficial in heart failure. Passive cardiac support devices and cardiac resynchronization therapy have been recently demonstrated to induce reverse remodeling of the left ventricle and may improve outcomes, including quality of life, functional status, and mortality. Summary Ventricular remodeling is strongly correlated with improvement in other heart failure outcomes. Early phase trials of novel therapeutics should carefully examine remodeling to obtain an efficacy signal. Larger clinical investigations should include remodeling metrics as endpoints and consider their use in a composite primary endpoint to reduce trial size.
引用
收藏
页码:223 / 229
页数:7
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