Relationship of ejection fraction and natriuretic peptide trajectories in heart failure with baseline reduced and mid-range ejection fraction.


Journal

American heart journal
ISSN: 1097-6744
Titre abrégé: Am Heart J
Pays: United States
ID NLM: 0370465

Informations de publication

Date de publication:
01 2022
Historique:
received: 21 12 2020
accepted: 21 08 2021
pubmed: 29 8 2021
medline: 8 4 2022
entrez: 28 8 2021
Statut: ppublish

Résumé

The prognostic importance of trajectories of neurohormones relative to left ventricular function over time in heart failure with reduced and mid-range EF (HFrEF and HFmrEF) is poorly defined. To evaluate left ventricular ejection fraction (LVEF) and B-type natriuretic peptide (BNP) trajectories in HFrEF and HFmrEF. Analyses of LVEF and BNP trajectories after incident HF admissions presenting with abnormal LV systolic function were performed using 3 methods: a Cox proportional hazards model with time-varying covariates, a dual longitudinal-survival model with shared random effects, and an unsupervised analysis to capture 3 discrete trajectories for each parameter. Among 1,158 patients (68.9 ± 13.0 years, 53.3% female), both time-varying LVEF measurements (P=.001) and log-transformed BNP measurements (p-values=2 × 10 Although LVEF trajectories have greater temporal variation, BNP trajectories provide additive prognostication and an even stronger association with survival times in heart failure patients with abnormal LV systolic function.

Sections du résumé

BACKGROUND
The prognostic importance of trajectories of neurohormones relative to left ventricular function over time in heart failure with reduced and mid-range EF (HFrEF and HFmrEF) is poorly defined.
OBJECTIVE
To evaluate left ventricular ejection fraction (LVEF) and B-type natriuretic peptide (BNP) trajectories in HFrEF and HFmrEF.
METHODS
Analyses of LVEF and BNP trajectories after incident HF admissions presenting with abnormal LV systolic function were performed using 3 methods: a Cox proportional hazards model with time-varying covariates, a dual longitudinal-survival model with shared random effects, and an unsupervised analysis to capture 3 discrete trajectories for each parameter.
RESULTS
Among 1,158 patients (68.9 ± 13.0 years, 53.3% female), both time-varying LVEF measurements (P=.001) and log-transformed BNP measurements (p-values=2 × 10
CONCLUSION
Although LVEF trajectories have greater temporal variation, BNP trajectories provide additive prognostication and an even stronger association with survival times in heart failure patients with abnormal LV systolic function.

Identifiants

pubmed: 34453882
pii: S0002-8703(21)00220-9
doi: 10.1016/j.ahj.2021.08.015
pmc: PMC8633031
mid: NIHMS1735717
pii:
doi:

Substances chimiques

Natriuretic Peptide, Brain 114471-18-0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-10

Subventions

Organisme : NHLBI NIH HHS
ID : R21 HL140445
Pays : United States
Organisme : NHLBI NIH HHS
ID : K01 HL142848
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL127654
Pays : United States
Organisme : NHLBI NIH HHS
ID : R56 HL135556
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL147104
Pays : United States
Organisme : NHLBI NIH HHS
ID : R25 HL126146
Pays : United States
Organisme : NHLBI NIH HHS
ID : L30 HL148881
Pays : United States

Informations de copyright

Copyright © 2021. Published by Elsevier Inc.

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Auteurs

Kenneth C Bilchick (KC)

Department of Medicine, University of Virginia Health System, Charlottesville, Virginia. Electronic address: bilchick@virginia.edu.

Patrick Stafford (P)

Department of Medicine, University of Virginia Health System, Charlottesville, Virginia.

Olusola Laja (O)

Department of Medicine, University of Virginia Health System, Charlottesville, Virginia.

Comfort Elumogo (C)

Department of Medicine, University of Virginia Health System, Charlottesville, Virginia.

Persey Bediako (P)

Department of Medicine, University of Virginia Health System, Charlottesville, Virginia.

Nora Tolbert (N)

Department of Medicine, University of Virginia Health System, Charlottesville, Virginia.

Douglas Sawch (D)

Department of Medicine, University of Virginia Health System, Charlottesville, Virginia.

Sthuthi David (S)

Department of Medicine, University of Virginia Health System, Charlottesville, Virginia.

Nishtha Sodhi (N)

Department of Medicine, University of Virginia Health System, Charlottesville, Virginia.

Anita Barber (A)

Department of Medicine, University of Virginia Health System, Charlottesville, Virginia.

Younghoon Kwon (Y)

Division of Cardiology, University of Washington, Seattle, Washington.

Nishaki Mehta (N)

Department of Medicine, William Beaumont Hospital, Royal Oak, Michigan.

Brandy Patterson (B)

Department of Medicine, University of Virginia Health System, Charlottesville, Virginia.

Khadijah Breathett (K)

Division of Cardiology, Department of Medicine, Sarver Heart Center, University of Arizona, Tucson.

Sula Mazimba (S)

Department of Medicine, University of Virginia Health System, Charlottesville, Virginia.

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Classifications MeSH