The Effect of Sacubitril/Valsartan on Left Ventricular Myocardial Deformation in Heart Failure with Preserved Ejection Fraction (PARAMOUNT trial)

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

The Effect of Sacubitril/Valsartan on Left Ventricular Myocardial Deformation in Heart Failure with Preserved Ejection Fraction (PARAMOUNT trial). / PARAMOUNT Investigators.

In: Journal of Cardiac Failure, Vol. 29, No. 6, 2023, p. 968-973.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

PARAMOUNT Investigators 2023, 'The Effect of Sacubitril/Valsartan on Left Ventricular Myocardial Deformation in Heart Failure with Preserved Ejection Fraction (PARAMOUNT trial)', Journal of Cardiac Failure, vol. 29, no. 6, pp. 968-973. https://doi.org/10.1016/j.cardfail.2023.03.019

APA

PARAMOUNT Investigators (2023). The Effect of Sacubitril/Valsartan on Left Ventricular Myocardial Deformation in Heart Failure with Preserved Ejection Fraction (PARAMOUNT trial). Journal of Cardiac Failure, 29(6), 968-973. https://doi.org/10.1016/j.cardfail.2023.03.019

Vancouver

PARAMOUNT Investigators. The Effect of Sacubitril/Valsartan on Left Ventricular Myocardial Deformation in Heart Failure with Preserved Ejection Fraction (PARAMOUNT trial). Journal of Cardiac Failure. 2023;29(6):968-973. https://doi.org/10.1016/j.cardfail.2023.03.019

Author

PARAMOUNT Investigators. / The Effect of Sacubitril/Valsartan on Left Ventricular Myocardial Deformation in Heart Failure with Preserved Ejection Fraction (PARAMOUNT trial). In: Journal of Cardiac Failure. 2023 ; Vol. 29, No. 6. pp. 968-973.

Bibtex

@article{5fc5d57b8cb04fa8a6170309b19cb0de,
title = "The Effect of Sacubitril/Valsartan on Left Ventricular Myocardial Deformation in Heart Failure with Preserved Ejection Fraction (PARAMOUNT trial)",
abstract = "Background: Global longitudinal strain (GLS) and global circumferential strain (GCS) have been shown to be impaired in heart failure with preserved ejection fraction. We sought to assess whether treating patients with heart failure with preserved ejection fraction with sacubitril/valsartan would significantly improve GLS and GCS compared with valsartan alone. Methods and Results: PARAMOUNT (Prospective Comparison of ARNI With ARB on Management of Heart Failure With Preserved Ejection Fraction Trial) was a phase II, randomized, parallel-group, double-blind multicenter trial in 301 patients with New York Heart Association functional class II–III heart failure, a left ventricular ejection fraction of 45%, and an N-terminal pro-B-type natriuretic peptide of ≥400 pg/mL. Participants were randomly assigned (1:1) to sacubitril/valsartan titrated to 200 mg twice daily or valsartan titrated to 160 mg twice daily for 36 weeks. We assessed changes in the GLS and the GCS from baseline to 36 weeks, adjusting for baseline value, in patients with sufficient imaging quality for 2-dimensitonal speckle tracking analysis at both timepoints (n = 60 sacubitril/valsartan, n = 75 valsartan only). GCS was significantly improved at 36 weeks in the sacubitril/valsartan group when compared with the valsartan group (Δ4.42%, 95% confidence interval [CI] 0.67–8.17, P =.021), with no significant difference observed in GLS (Δ0.25%, 95% CI, –1.19 to 1.70, P =.73). Patients with a history of hospitalization for heart failure had a differentially greater improvement in GCS when treated with sacubitril/valsartan. Conclusions: In patients with heart failure with preserved ejection fraction, sacubitril/valsartan improved GCS but not GLS when compared with valsartan during a 36-week period. This trial is registered at ClinicalTrials.gov, NCT00887588.",
keywords = "echocardiography, HFpEF, randomizel clinical trial, sacubitril, strain",
author = "Tor Biering-S{\o}rensen and {H{\o}jbjerg Lassen}, {Mats Christian} and Amil Sham and Brian Claggett and Michael Zile and Burkert Pieske and Elisabeth Pieske-Kraigher and Adriaan Voors and Victor Shi and Martin Lefkowitz and Milton Packer and McMurray, {John J.V.} and Solomon, {Scott D.} and {PARAMOUNT Investigators}",
note = "Publisher Copyright: {\textcopyright} 2023 The Author(s)",
year = "2023",
doi = "10.1016/j.cardfail.2023.03.019",
language = "English",
volume = "29",
pages = "968--973",
journal = "Journal of Cardiac Failure",
issn = "1071-9164",
publisher = "Churchill Livingstone",
number = "6",

}

RIS

TY - JOUR

T1 - The Effect of Sacubitril/Valsartan on Left Ventricular Myocardial Deformation in Heart Failure with Preserved Ejection Fraction (PARAMOUNT trial)

AU - Biering-Sørensen, Tor

AU - Højbjerg Lassen, Mats Christian

AU - Sham, Amil

AU - Claggett, Brian

AU - Zile, Michael

AU - Pieske, Burkert

AU - Pieske-Kraigher, Elisabeth

AU - Voors, Adriaan

AU - Shi, Victor

AU - Lefkowitz, Martin

AU - Packer, Milton

AU - McMurray, John J.V.

AU - Solomon, Scott D.

AU - PARAMOUNT Investigators

N1 - Publisher Copyright: © 2023 The Author(s)

PY - 2023

Y1 - 2023

N2 - Background: Global longitudinal strain (GLS) and global circumferential strain (GCS) have been shown to be impaired in heart failure with preserved ejection fraction. We sought to assess whether treating patients with heart failure with preserved ejection fraction with sacubitril/valsartan would significantly improve GLS and GCS compared with valsartan alone. Methods and Results: PARAMOUNT (Prospective Comparison of ARNI With ARB on Management of Heart Failure With Preserved Ejection Fraction Trial) was a phase II, randomized, parallel-group, double-blind multicenter trial in 301 patients with New York Heart Association functional class II–III heart failure, a left ventricular ejection fraction of 45%, and an N-terminal pro-B-type natriuretic peptide of ≥400 pg/mL. Participants were randomly assigned (1:1) to sacubitril/valsartan titrated to 200 mg twice daily or valsartan titrated to 160 mg twice daily for 36 weeks. We assessed changes in the GLS and the GCS from baseline to 36 weeks, adjusting for baseline value, in patients with sufficient imaging quality for 2-dimensitonal speckle tracking analysis at both timepoints (n = 60 sacubitril/valsartan, n = 75 valsartan only). GCS was significantly improved at 36 weeks in the sacubitril/valsartan group when compared with the valsartan group (Δ4.42%, 95% confidence interval [CI] 0.67–8.17, P =.021), with no significant difference observed in GLS (Δ0.25%, 95% CI, –1.19 to 1.70, P =.73). Patients with a history of hospitalization for heart failure had a differentially greater improvement in GCS when treated with sacubitril/valsartan. Conclusions: In patients with heart failure with preserved ejection fraction, sacubitril/valsartan improved GCS but not GLS when compared with valsartan during a 36-week period. This trial is registered at ClinicalTrials.gov, NCT00887588.

AB - Background: Global longitudinal strain (GLS) and global circumferential strain (GCS) have been shown to be impaired in heart failure with preserved ejection fraction. We sought to assess whether treating patients with heart failure with preserved ejection fraction with sacubitril/valsartan would significantly improve GLS and GCS compared with valsartan alone. Methods and Results: PARAMOUNT (Prospective Comparison of ARNI With ARB on Management of Heart Failure With Preserved Ejection Fraction Trial) was a phase II, randomized, parallel-group, double-blind multicenter trial in 301 patients with New York Heart Association functional class II–III heart failure, a left ventricular ejection fraction of 45%, and an N-terminal pro-B-type natriuretic peptide of ≥400 pg/mL. Participants were randomly assigned (1:1) to sacubitril/valsartan titrated to 200 mg twice daily or valsartan titrated to 160 mg twice daily for 36 weeks. We assessed changes in the GLS and the GCS from baseline to 36 weeks, adjusting for baseline value, in patients with sufficient imaging quality for 2-dimensitonal speckle tracking analysis at both timepoints (n = 60 sacubitril/valsartan, n = 75 valsartan only). GCS was significantly improved at 36 weeks in the sacubitril/valsartan group when compared with the valsartan group (Δ4.42%, 95% confidence interval [CI] 0.67–8.17, P =.021), with no significant difference observed in GLS (Δ0.25%, 95% CI, –1.19 to 1.70, P =.73). Patients with a history of hospitalization for heart failure had a differentially greater improvement in GCS when treated with sacubitril/valsartan. Conclusions: In patients with heart failure with preserved ejection fraction, sacubitril/valsartan improved GCS but not GLS when compared with valsartan during a 36-week period. This trial is registered at ClinicalTrials.gov, NCT00887588.

KW - echocardiography

KW - HFpEF

KW - randomizel clinical trial

KW - sacubitril

KW - strain

UR - http://www.scopus.com/inward/record.url?scp=85159173189&partnerID=8YFLogxK

U2 - 10.1016/j.cardfail.2023.03.019

DO - 10.1016/j.cardfail.2023.03.019

M3 - Journal article

C2 - 37031887

AN - SCOPUS:85159173189

VL - 29

SP - 968

EP - 973

JO - Journal of Cardiac Failure

JF - Journal of Cardiac Failure

SN - 1071-9164

IS - 6

ER -

ID: 347753037