Sacubitril/valsartan versus enalapril on exercise capacity in patients with heart failure with reduced ejection

Marcelo Rodrigues Dos Santos1, Maria-Janieire de Nazaré Nunes Alves1, Camila Paixão Jordão1

  • 1Instituto Do Coração (InCor), Hospital Das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.

Insights

Sacubitril/valsartan did not significantly improve exercise capacity, measured by peak oxygen consumption and the 6-minute walk test, compared to enalapril in patients with heart failure with reduced ejection fraction over 24 weeks.

Area of Science:

  • Cardiology
  • Exercise Physiology
  • Pharmacology

Background:

  • Sacubitril/valsartan is known to reduce mortality in heart failure with reduced ejection fraction (HFrEF).
  • The impact of sacubitril/valsartan on exercise capacity in HFrEF patients compared to enalapril remains unclear.

Purpose of the Study:

  • To compare the effects of sacubitril/valsartan versus enalapril on exercise capacity in patients with HFrEF.
  • To evaluate changes in peak oxygen consumption (VO2) and 6-minute walk test (6-MWT) performance.

Main Methods:

  • A randomized trial involving 52 HFrEF participants (left ventricular ejection fraction <40%).
  • Participants received either sacubitril/valsartan (target 400 mg/day) or enalapril (target 40 mg/day) for 24 weeks.
  • Exercise capacity assessed via cardiopulmonary exercise testing (peak VO2) and 6-MWT.

Main Results:

  • Both sacubitril/valsartan and enalapril showed increases in peak VO2 and 6-MWT over 24 weeks.
  • No statistically significant differences in the improvement of peak VO2 or 6-MWT were observed between the sacubitril/valsartan and enalapril groups at 12 or 24 weeks.
  • While sacubitril/valsartan showed a trend towards greater improvement in 6-MWT at 24 weeks, this difference was not statistically significant.

Conclusions:

  • Sacubitril/valsartan did not offer substantial improvements in peak VO2 or 6-MWT compared to enalapril in HFrEF patients.
  • Exercise capacity benefits observed were similar between the two treatment groups over the 24-week study period.

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