NT-proBNP Goal Achievement Is Associated With Significant Reverse Remodeling and Improved Clinical Outcomes in HFrEF.


Journal

JACC. Heart failure
ISSN: 2213-1787
Titre abrégé: JACC Heart Fail
Pays: United States
ID NLM: 101598241

Informations de publication

Date de publication:
02 2019
Historique:
received: 27 07 2018
revised: 05 10 2018
accepted: 12 10 2018
pubmed: 7 1 2019
medline: 17 3 2020
entrez: 7 1 2019
Statut: ppublish

Résumé

This study aims to assess the association between biomarker-guided therapy and left ventricular (LV) remodeling. In patients with heart failure with reduced ejection fraction (HFrEF), it is unclear if lowering natriuretic peptides reflects structural and functional changes in the heart. This study aims to assess the association between biomarker-guided therapy and left ventricular (LV) remodeling. The GUIDE-IT (Guiding Evidence Based Therapy Using Biomarker Intensified Treatment in Heart Failure) Echo Substudy was a multicenter study that randomized 268 patients with HFrEF (EF ≤40%) to either pro-B-type natriuretic peptide (NT-proBNP)-guided treatment or usual care. Echocardiograms were performed at baseline and 12 months in 124 patients. Remodeling indices and clinical outcomes were compared between treatment arms and by achievement of the NT-proBNP goal of <1,000 pg/ml at 12 months. At 12 months, the changes in EF and LV volumes were similar between the biomarker-guided and usual care arms with no difference in clinical outcomes; however, lowering NT-proBNP to <1,000 pg/ml, regardless of treatment strategy, was associated with a significantly greater increase in EF compared with those not reaching goal (9.9 ± 8.8% vs. 2.9 ± 7.9%; p < 0.001) and lower LV volumes. The extent of reverse remodeling correlated with the change in NT-proBNP: a decrease of 1,000 pg/ml was associated with an increase in EF of 6.7% and a reduction in systolic and diastolic volumes of 17.3 ml/m Among patients with HFrEF, lowering NT-proBNP to <1,000 pg/ml by 12 months was associated with significant reverse remodeling and improved outcomes. A greater reduction in NT-proBNP was associated with more extensive reverse remodeling. (Guiding Evidence Based Therapy Using Biomarker Intensified Treatment [GUIDE-IT]; NCT01685840).

Sections du résumé

OBJECTIVES
This study aims to assess the association between biomarker-guided therapy and left ventricular (LV) remodeling.
BACKGROUND
In patients with heart failure with reduced ejection fraction (HFrEF), it is unclear if lowering natriuretic peptides reflects structural and functional changes in the heart. This study aims to assess the association between biomarker-guided therapy and left ventricular (LV) remodeling.
METHODS
The GUIDE-IT (Guiding Evidence Based Therapy Using Biomarker Intensified Treatment in Heart Failure) Echo Substudy was a multicenter study that randomized 268 patients with HFrEF (EF ≤40%) to either pro-B-type natriuretic peptide (NT-proBNP)-guided treatment or usual care. Echocardiograms were performed at baseline and 12 months in 124 patients. Remodeling indices and clinical outcomes were compared between treatment arms and by achievement of the NT-proBNP goal of <1,000 pg/ml at 12 months.
RESULTS
At 12 months, the changes in EF and LV volumes were similar between the biomarker-guided and usual care arms with no difference in clinical outcomes; however, lowering NT-proBNP to <1,000 pg/ml, regardless of treatment strategy, was associated with a significantly greater increase in EF compared with those not reaching goal (9.9 ± 8.8% vs. 2.9 ± 7.9%; p < 0.001) and lower LV volumes. The extent of reverse remodeling correlated with the change in NT-proBNP: a decrease of 1,000 pg/ml was associated with an increase in EF of 6.7% and a reduction in systolic and diastolic volumes of 17.3 ml/m
CONCLUSIONS
Among patients with HFrEF, lowering NT-proBNP to <1,000 pg/ml by 12 months was associated with significant reverse remodeling and improved outcomes. A greater reduction in NT-proBNP was associated with more extensive reverse remodeling. (Guiding Evidence Based Therapy Using Biomarker Intensified Treatment [GUIDE-IT]; NCT01685840).

Identifiants

pubmed: 30611722
pii: S2213-1779(18)30784-4
doi: 10.1016/j.jchf.2018.10.014
pii:
doi:

Substances chimiques

Biomarkers 0
Peptide Fragments 0
Protein Precursors 0
pro-brain natriuretic peptide (1-76) 0
Natriuretic Peptide, Brain 114471-18-0

Banques de données

ClinicalTrials.gov
['NCT01685840']

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

158-168

Informations de copyright

Copyright © 2019 American College of Cardiology Foundation. All rights reserved.

Auteurs

Melissa A Daubert (MA)

Duke University Medical Center, Durham, North Carolina; Duke Clinical Research Institute, Durham, North Carolina. Electronic address: melissa.daubert@duke.edu.

Kirkwood Adams (K)

University of North Carolina, Chapel Hill, North Carolina.

Eric Yow (E)

Duke Clinical Research Institute, Durham, North Carolina.

Huiman X Barnhart (HX)

Duke University Medical Center, Durham, North Carolina; Duke Clinical Research Institute, Durham, North Carolina.

Pamela S Douglas (PS)

Duke University Medical Center, Durham, North Carolina; Duke Clinical Research Institute, Durham, North Carolina.

Susan Rimmer (S)

Duke Clinical Research Institute, Durham, North Carolina.

Casey Norris (C)

Duke Clinical Research Institute, Durham, North Carolina.

Lawton Cooper (L)

National Heart, Lung, and Blood Institute, Bethesda, Maryland.

Eric Leifer (E)

National Heart, Lung, and Blood Institute, Bethesda, Maryland.

Patrice Desvigne-Nickens (P)

National Heart, Lung, and Blood Institute, Bethesda, Maryland.

Kevin Anstrom (K)

Duke University Medical Center, Durham, North Carolina; Duke Clinical Research Institute, Durham, North Carolina.

Mona Fiuzat (M)

Duke University Medical Center, Durham, North Carolina.

Justin Ezekowitz (J)

University of Alberta, Edmonton, Alberta, Canada.

Daniel B Mark (DB)

Duke University Medical Center, Durham, North Carolina; Duke Clinical Research Institute, Durham, North Carolina.

Christopher M O'Connor (CM)

Duke University Medical Center, Durham, North Carolina; Inova Heart and Vascular Institute, Falls Church, Virginia.

James Januzzi (J)

Massachusetts General Hospital, Boston, Massachusetts.

G Michael Felker (GM)

Duke University Medical Center, Durham, North Carolina; Duke Clinical Research Institute, Durham, North Carolina.

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Classifications MeSH