Differences in NT-proBNP Response and Prognosis in Men and Women With Heart Failure With Reduced Ejection Fraction.


Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
18 05 2021
Historique:
pubmed: 7 5 2021
medline: 28 10 2021
entrez: 6 5 2021
Statut: ppublish

Résumé

Background NT-proBNP (N-terminal pro-B-type natriuretic peptide) is a prognostic biomarker in heart failure (HF) with reduced ejection fraction. However, it is unclear whether there is a sex difference in NT-proBNP response and whether the therapeutic goal of NT-proBNP ≤1000 pg/mL has equivalent prognostic value in men and women with HF with reduced ejection fraction. Methods and Results In a secondary analysis of the GUIDE-IT (Guiding Evidence Based Therapy Using Biomarker Intensified Treatment) trial we analyzed trends in NT-proBNP and goal attainment by sex. Differences in clinical characteristics, HF treatment, and time to all-cause death or HF hospitalization were compared. Landmark analysis at 3 months determined the prognostic value of early NT-proBNP goal achievement in men and women. Of the 286 (32%) women and 608 (68%) men in the GUIDE-IT trial, women were more likely to have a nonischemic cause and shorter duration of HF. Guideline-directed medical therapy was less intense over time in women. The absolute NT-proBNP values were consistently lower in women; however, the change in NT-proBNP and clinical outcomes were similar. After adjustment, women achieving the NT-proBNP goal had an 82% reduction in death or HF hospitalization compared with a 59% reduction in men. Conclusions Men and women with HF with reduced ejection fraction had a similar NT-proBNP response despite less intensive HF treatment among women. However, compared with men, the early NT-proBNP goal of ≤1000 pg/mL had greater prognostic value in women. Future efforts should be aimed at intensifying guideline-directed medical therapy in women, which may result in greater NT-proBNP reductions and improved outcomes in women with HF with reduced ejection fraction. Registration URL: https://www.clinicaltrials.gov; Unique identifier: NCT01685840.

Identifiants

pubmed: 33955231
doi: 10.1161/JAHA.120.019712
pmc: PMC8200692
doi:

Substances chimiques

Adrenergic beta-Antagonists 0
Angiotensin Receptor Antagonists 0
Angiotensin-Converting Enzyme Inhibitors 0
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, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e019712

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Auteurs

Melissa A Daubert (MA)

Duke University Medical Center Durham NC.
Duke Clinical Research Institute Durham NC.

Eric Yow (E)

Duke Clinical Research Institute Durham NC.

Huiman X Barnhart (HX)

Duke University Medical Center Durham NC.
Duke Clinical Research Institute Durham NC.

Ileana L Piña (IL)

Wayne State University Detroit MI.

Tariq Ahmad (T)

Yale School of Medicine New Haven CT.

Eric Leifer (E)

National Heart, Lung and Blood Institute Bethesda MD.

Lawton Cooper (L)

National Heart, Lung and Blood Institute Bethesda MD.

Patrice Desvigne-Nickens (P)

National Heart, Lung and Blood Institute Bethesda MD.

Mona Fiuzat (M)

Duke University Medical Center Durham NC.

Kirkwood Adams (K)

University of North Carolina Chapel Hill NC.

Justin Ezekowitz (J)

University of Alberta Edmonton Alberta Canada.

David J Whellan (DJ)

Thomas Jefferson University Philadelphia PA.

James L Januzzi (JL)

Massachusetts General Hospital Boston MA.

Christopher M O'Connor (CM)

Duke University Medical Center Durham NC.
Inova Heart and Vascular Institute Falls Church VA.

G Michael Felker (GM)

Duke University Medical Center Durham NC.
Duke Clinical Research Institute Durham NC.

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