Echocardiographic evaluation of the effects of sacubitril-valsartan on vascular properties in heart failure patients.
Adult
Aged
Aminobutyrates
/ adverse effects
Angiotensin II Type 1 Receptor Blockers
/ adverse effects
Biphenyl Compounds
Case-Control Studies
Drug Combinations
Echocardiography
Female
Heart Failure
/ diagnostic imaging
Humans
Male
Middle Aged
Neprilysin
/ antagonists & inhibitors
Predictive Value of Tests
Prospective Studies
Protease Inhibitors
/ adverse effects
Tetrazoles
/ adverse effects
Time Factors
Treatment Outcome
Valsartan
Vascular Stiffness
/ drug effects
Vasodilation
/ drug effects
Aorta
Aortic distensibility
Entresto
Vascular stiffness
Journal
The international journal of cardiovascular imaging
ISSN: 1875-8312
Titre abrégé: Int J Cardiovasc Imaging
Pays: United States
ID NLM: 100969716
Informations de publication
Date de publication:
Feb 2020
Feb 2020
Historique:
received:
09
07
2019
accepted:
22
09
2019
pubmed:
5
10
2019
medline:
12
3
2020
entrez:
5
10
2019
Statut:
ppublish
Résumé
Increased vascular stiffness is known to be an independent predictor of mortality in patients with heart failure with reduced ejection fraction (HFrEF). The effects of sacubitril-valsartan on vascular structure and function have not been systematically studied in this patient population. We hypothesized that aortic distensibility (AD) and fractional area change (AFAC), as assessed by 2D transthoracic echocardiography (TTE), would improve over time in HFrEF patients on sacubitril-valsartan therapy, due to the vasodilatory properties of the medication. We prospectively studied 30 patients with HFrEF (25 < EF < 40%) on optimal guideline-directed medical therapy who were subsequently started on sacubitril-valsartan. Patients underwent serial 2D TTE imaging at baseline, 3 and 6 months following therapy initiation. Ascending aortic diameters were measured 3 cm above the aortic valve in the parasternal long-axis view and used to calculate AD and AFAC, two markers of vascular compliance. For reference, we also measured AD and AFAC in 30 healthy, age and gender-matched controls at a single time point. Normal controls had significantly higher values of AD and AFAC than HFrEF patients at baseline (AD: 4.0 ± 1.1 vs. 2.2 ± 0.9 cm
Identifiants
pubmed: 31583499
doi: 10.1007/s10554-019-01708-4
pii: 10.1007/s10554-019-01708-4
pmc: PMC7135917
mid: NIHMS1565676
doi:
Substances chimiques
Aminobutyrates
0
Angiotensin II Type 1 Receptor Blockers
0
Biphenyl Compounds
0
Drug Combinations
0
Protease Inhibitors
0
Tetrazoles
0
Valsartan
80M03YXJ7I
Neprilysin
EC 3.4.24.11
sacubitril and valsartan sodium hydrate drug combination
WB8FT61183
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
271-278Subventions
Organisme : NHLBI NIH HHS
ID : T32 HL007381
Pays : United States
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