4.5 Article

Reverse Cardiac Remodeling Following Initiation of Sacubitril/Valsartan in Patients With Heart Failure With and Without Diabetes

Journal

JACC-HEART FAILURE
Volume 9, Issue 2, Pages 137-145

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.jchf.2020.09.014

Keywords

cardiac remodeling; diabetes; heart failure; NT-proBNP; sacubitril/valsartan

Funding

  1. National Heart, Lung, and Blood Institute
  2. American Heart Association
  3. Merck
  4. Amgen
  5. Cytokinetics
  6. Roche Diagnostics
  7. Dennis and Marilyn Barry Fund in Cardiovascular Research
  8. Alnylam
  9. AstraZeneca
  10. Bellerophon
  11. Bayer
  12. Bristol Myers Squibb
  13. Celladon
  14. Eidos
  15. Gilead
  16. GlaxoSmithKline
  17. Ionis
  18. Lilly
  19. Lone Star Heart
  20. Mesoblast
  21. MyoKardia
  22. NIH/NHLBI
  23. Neurotronik
  24. Novartis
  25. Respicardia
  26. Sanofi Pasteur
  27. Theracos
  28. Roche
  29. Abbott
  30. Janssen
  31. Singulex
  32. Prevencio

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The study found that patients with heart failure and reduced ejection fraction (HFrEF) with or without type 2 diabetes mellitus (T2DM) can both benefit from sacubitril/valsartan therapy in terms of N-terminal pro-b-type natriuretic peptide levels, cardiac remodeling measures, and overall health status improvement.
OBJECTIVE This study sought to determine whether patients with heart failure and reduced ejection fraction (HFrEF) with type 2 diabetes mellitus (T2DM) have similar reverse cardiac remodeling with sacubitril/valsartan as patients without T2DM. BACKGROUND Sacubitril/valsartan promotes reverse cardiac remodeling and improves outcomes in patients with HFrEF. Patients with HFrEF with T2DM have worse prognosis than those without T2DM. METHODS In this post hoc analysis of PROVE-HF (Prospective Study of Biomarkers, Symptom Improvement, and Ventricular Remodeling During Sacubitril/Valsartan Therapy for Heart Failure), we examined changes in N-terminal pro-b-type natriuretic peptide (NT-proBNP), measures of cardiac remodeling, and Kansas City Cardiomyopathy Questionnaire Overall Summary (KCCQ-OS) scores from baseline to 12 months following initiation of sacubitril/valsartan between patients with HFrEF with and without T2DM. Using latent growth curve modeling, we evaluated the longitudinal association between changes in NT-proBNP, left ventricular ejection fraction, and KCCQ-OS. RESULTS Among 794 patients enrolled, 361 (45.5%) had T2DM. NT-proBNP concentrations were modestly higher at baseline among patients with T2DM but were reduced after initiation of sacubitril/valsartan. Cross-sectional improvement was observed in left ventricular ejection fraction (T2DM: 283% at baseline and 37% at 12 months vs. non-T2DM: 28.1% at baseline and 38.3% at 12 months) and KCCQ-OS (T2DM: 71 at baseline and 83 at 12 months vs. non-T2DM: 76 at baseline and 88 at 12 months). Similar changes were also observed for other echocardiographic measures. In longitudinal analyses, the average NT-proBNP change was similar in patients with T2DM (-5.6% vs. -7.1% per 90-day interval; p 0.64), whereas improvements in KCCQ-OS scores were slightly smaller (2.1 vs. 3.46 per 90-day interval; p = 0.07). CONCLUSIONS Sacubitril/valsartan favorably affects natriuretic peptide levels, reverse cardiac remodeling, and health status in patients with HFrEF with and without T2DM. (C) 2021 The Authors. Published by Elsevier on behalf of the American College of Cardiology Foundation.

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