-
Je něco špatně v tomto záznamu ?
Effect of vericiguat on left ventricular structure and function in patients with heart failure with reduced ejection fraction: The VICTORIA echocardiographic substudy
B. Pieske, E. Pieske-Kraigher, CSP. Lam, V. Melenovský, K. Sliwa, Y. Lopatin, JL. Arango, MC. Bahit, CM. O'Connor, MJ. Patel, L. Roessig, DA. Morris, M. Kropf, CM. Westerhout, Y. Zheng, PW. Armstrong, VICTORIA Study Group
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Medline Complete (EBSCOhost)
od 2000-03-01 do Před 1 rokem
Wiley Free Content
od 1999 do Před 1 rokem
PubMed
36994634
DOI
10.1002/ejhf.2836
Knihovny.cz E-zdroje
- MeSH
- echokardiografie MeSH
- funkce levé komory srdeční MeSH
- heterocyklické sloučeniny bicyklické * MeSH
- lidé MeSH
- srdeční selhání * diagnostické zobrazování farmakoterapie chemicky indukované MeSH
- tepový objem MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
AIM: Vericiguat significantly reduced the primary composite outcome of heart failure (HF) hospitalization or cardiovascular death in the VICTORIA trial. It is unknown if these outcome benefits are related to reverse left ventricular (LV) remodelling with vericiguat in patients with HF with reduced ejection fraction (HFrEF). The aim of this study was to compare the effects of vericiguat versus placebo on LV structure and function after 8 months of therapy in patients with HFrEF. METHODS AND RESULTS: Standardized transthoracic echocardiography (TTE) was performed at baseline and after 8 months of therapy in a subset of HFrEF patients in VICTORIA. The co-primary endpoints were changes in LV end-systolic volume index (LVESVI) and LV ejection fraction (LVEF). Quality assurance and central reading were performed by an echocardiographic core laboratory blinded to treatment assignment. A total of 419 patients (208 vericiguat, 211 placebo) with high-quality paired TTE at baseline and 8 months were included. Baseline clinical characteristics were well balanced between treatment groups and echocardiographic characteristics were representative of patients with HFrEF. LVESVI significantly declined (60.7 ± 26.8 to 56.8 ± 30.4 ml/m2 ; p < 0.01) and LVEF significantly increased (33.0 ± 9.4% to 36.1 ± 10.2%; p < 0.01) in the vericiguat group, but similarly in the placebo group (absolute changes for vericiguat vs. placebo: LVESVI -3.8 ± 15.4 vs. -7.1 ± 20.5 ml/m2 ; p = 0.07 and LVEF +3.2 ± 8.0% vs. +2.4 ± 7.6%; p = 0.31). The absolute rate per 100 patient-years of the primary composite endpoint at 8 months tended to be lower in the vericiguat group (19.8) than the placebo group (29.6) (p = 0.07). CONCLUSIONS: In this pre-specified echocardiographic study, significant improvements in LV structure and function occurred over 8 months in both vericiguat and placebo in a high-risk HFrEF population with recent worsening HF. Further studies are warranted to define the mechanisms of vericiguat's benefit in HFrEF.
Canadian VIGOUR Centre University of Alberta Edmonton AB Canada
Cape Heart Institute University of Cape Town Cape Town South Africa
Charité University Medicine German Heart Center Berlin Germany
Department of Cardiology Institute for Clinical and Experimental Medicine Prague Czech Republic
INECO Neurociencias Oroño Fundación INECO Rosario Argentina
Inova Heart and Vascular Institute Falls Church VA USA
Merck and Co Inc Rahway NJ USA
National Heart Centre Singapore and Duke National University of Singapore Singapore Singapore
Unidad de Cirugía Cardiovascular de Guatemala Guatemala City Guatemala
Volgograd State Medical University Volgograd Regional Cardiology Center Volgograd Russian Federation
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc23017019
- 003
- CZ-PrNML
- 005
- 20231026105333.0
- 007
- ta
- 008
- 231013s2023 enk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1002/ejhf.2836 $2 doi
- 035 __
- $a (PubMed)36994634
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a enk
- 100 1_
- $a Pieske, Burkert $u Charité University Medicine, German Heart Center, Berlin, Germany
- 245 10
- $a Effect of vericiguat on left ventricular structure and function in patients with heart failure with reduced ejection fraction: The VICTORIA echocardiographic substudy / $c B. Pieske, E. Pieske-Kraigher, CSP. Lam, V. Melenovský, K. Sliwa, Y. Lopatin, JL. Arango, MC. Bahit, CM. O'Connor, MJ. Patel, L. Roessig, DA. Morris, M. Kropf, CM. Westerhout, Y. Zheng, PW. Armstrong, VICTORIA Study Group
- 520 9_
- $a AIM: Vericiguat significantly reduced the primary composite outcome of heart failure (HF) hospitalization or cardiovascular death in the VICTORIA trial. It is unknown if these outcome benefits are related to reverse left ventricular (LV) remodelling with vericiguat in patients with HF with reduced ejection fraction (HFrEF). The aim of this study was to compare the effects of vericiguat versus placebo on LV structure and function after 8 months of therapy in patients with HFrEF. METHODS AND RESULTS: Standardized transthoracic echocardiography (TTE) was performed at baseline and after 8 months of therapy in a subset of HFrEF patients in VICTORIA. The co-primary endpoints were changes in LV end-systolic volume index (LVESVI) and LV ejection fraction (LVEF). Quality assurance and central reading were performed by an echocardiographic core laboratory blinded to treatment assignment. A total of 419 patients (208 vericiguat, 211 placebo) with high-quality paired TTE at baseline and 8 months were included. Baseline clinical characteristics were well balanced between treatment groups and echocardiographic characteristics were representative of patients with HFrEF. LVESVI significantly declined (60.7 ± 26.8 to 56.8 ± 30.4 ml/m2 ; p < 0.01) and LVEF significantly increased (33.0 ± 9.4% to 36.1 ± 10.2%; p < 0.01) in the vericiguat group, but similarly in the placebo group (absolute changes for vericiguat vs. placebo: LVESVI -3.8 ± 15.4 vs. -7.1 ± 20.5 ml/m2 ; p = 0.07 and LVEF +3.2 ± 8.0% vs. +2.4 ± 7.6%; p = 0.31). The absolute rate per 100 patient-years of the primary composite endpoint at 8 months tended to be lower in the vericiguat group (19.8) than the placebo group (29.6) (p = 0.07). CONCLUSIONS: In this pre-specified echocardiographic study, significant improvements in LV structure and function occurred over 8 months in both vericiguat and placebo in a high-risk HFrEF population with recent worsening HF. Further studies are warranted to define the mechanisms of vericiguat's benefit in HFrEF.
- 650 _2
- $a lidé $7 D006801
- 650 12
- $a srdeční selhání $x diagnostické zobrazování $x farmakoterapie $x chemicky indukované $7 D006333
- 650 _2
- $a tepový objem $7 D013318
- 650 12
- $a heterocyklické sloučeniny bicyklické $7 D006574
- 650 _2
- $a funkce levé komory srdeční $7 D016277
- 650 _2
- $a echokardiografie $7 D004452
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Pieske-Kraigher, Elisabeth $u Charité University Medicine, German Heart Center, Berlin, Germany
- 700 1_
- $a Lam, Carolyn S P $u National Heart Centre Singapore and Duke-National University of Singapore, Singapore, Singapore
- 700 1_
- $a Melenovský, Vojtěch $u Department of Cardiology, Institute for Clinical and Experimental Medicine, Prague, Czech Republic
- 700 1_
- $a Sliwa, Karen $u Cape Heart Institute, University of Cape Town, Cape Town, South Africa
- 700 1_
- $a Lopatin, Yuri $u Volgograd State Medical University, Volgograd Regional Cardiology Center, Volgograd, Russian Federation
- 700 1_
- $a Arango, Juan Luis $u Unidad de Cirugía Cardiovascular de Guatemala, Guatemala City, Guatemala
- 700 1_
- $a Bahit, M Cecilia $u INECO Neurociencias Oroño, Fundación INECO, Rosario, Argentina
- 700 1_
- $a O'Connor, Christopher M $u Inova Heart and Vascular Institute, Falls Church, VA, USA
- 700 1_
- $a Patel, Mahesh J $u Merck & Co., Inc., Rahway, NJ, USA
- 700 1_
- $a Roessig, Lothar $u Bayer AG, Wuppertal, Germany
- 700 1_
- $a Morris, Daniel A $u Charité University Medicine, German Heart Center, Berlin, Germany
- 700 1_
- $a Kropf, Martin $u Charité University Medicine, German Heart Center, Berlin, Germany
- 700 1_
- $a Westerhout, Cynthia M $u Canadian VIGOUR Centre, University of Alberta, Edmonton, AB, Canada
- 700 1_
- $a Zheng, Yinggan $u Canadian VIGOUR Centre, University of Alberta, Edmonton, AB, Canada
- 700 1_
- $a Armstrong, Paul W $u Canadian VIGOUR Centre, University of Alberta, Edmonton, AB, Canada
- 710 2_
- $a VICTORIA Study Group
- 773 0_
- $w MED00006634 $t European journal of heart failure $x 1879-0844 $g Roč. 25, č. 7 (2023), s. 1012-1021
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/36994634 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y - $z 0
- 990 __
- $a 20231013 $b ABA008
- 991 __
- $a 20231026105328 $b ABA008
- 999 __
- $a ok $b bmc $g 2000505 $s 1203381
- BAS __
- $a 3
- BAS __
- $a PreBMC-MEDLINE
- BMC __
- $a 2023 $b 25 $c 7 $d 1012-1021 $e 20230418 $i 1879-0844 $m European journal of heart failure $n Eur J Heart Fail $x MED00006634
- LZP __
- $a Pubmed-20231013