4.7 Article

Natriuretic Peptide Response and Outcomes in Chronic Heart Failure With Reduced Ejection Fraction

Journal

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
Volume 74, Issue 9, Pages 1205-1217

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jacc.2019.06.055

Keywords

heart failure; natriuretic peptides; outcomes

Funding

  1. National Heart, Lung, and Blood Institute (NHLBI) [H105448, HL105451, HL105457]
  2. Roche Diagnostics
  3. Hutter Family Professorship
  4. Abbott Diagnostics
  5. Singulex
  6. Prevencio
  7. Novartis
  8. Cleveland Heart Labs
  9. NHLBI
  10. Merck
  11. Bayer
  12. Amgen
  13. Otsuka
  14. Boehringer Ingelheim
  15. Bristol-Myers Squibb
  16. CIHR
  17. Oxygen Therapeutics
  18. HeartFlow
  19. National Institute on Aging
  20. CVR Global
  21. ResMed
  22. Aegerion Pharmaceuticals
  23. National Institutes of Health
  24. American Heart Association

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BACKGROUND The GUIDE-IT (GUIDing Evidence Based Therapy Using Biomarker Intensified Treatment in Heart Failure) trial demonstrated that a strategy to guide application of guideline-directed medical therapy (GDMT) by reducing amino-terminal pro-B-type natriuretic peptide (NT-proBNP) was not superior to GDMT alone. OBJECTIVES The purpose of this study was to examine the prognostic meaning of NT-proBNP changes following heart failure (HF) therapy intensification relative to the goal NT-proBNP value of 1,000 pg/ml explored in the GUIDE-IT trial. METHODS A total of 638 study participants were included who were alive and had available NT-proBNP results 90 days after randomization. Rates of subsequent cardiovascular (CV) death/HF hospitalization or all-cause mortality during follow-up and Kansas City Cardiomyopathy Questionnaire (KCCQ) overall scores were analyzed. RESULTS A total of 198 (31.0%) subjects had an NT-proBNP <= 1,000 pg/ml at 90 days with no difference in achievement of NT-proBNP goal between the biomarker-guided and usual care arms. NT-proBNP <= 1,000 pg/ml by 90 days was associated with longer freedom from CV/HF hospitalization or all-cause mortality (p < 0.001 for both) and lower adjusted hazard of subsequent HF hospitalization/CV death (hazard ratio: 0.26; 95% confidence interval: 0.15 to 0.46; p < 0.001) and all-cause mortality (hazard ratio: 0.34; 95% confidence interval: 0.15 to 0.77; p = 0.009). Regardless of elevated baseline concentration, an NT-proBNP <= 1,000 pg/ml at 90 days was associated with better outcomes and significantly better KCCQ overall scores (p = 0.02). CONCLUSIONS Patients with heart failure with reduced ejection fraction whose NT-proBNP levels decreased to <= 1,000 pg/ml during GDMT had better outcomes. These findings may help to understand the results of the GUIDE-IT trial. (Guiding Evidence Based Therapy Using Biomarker Intensified Treatment [GUIDE-IT]; NCT01685840) (C) 2019 by the American College of Cardiology Foundation.

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