Effects of the sodium-glucose cotransporter 2 inhibitor empagliflozin on vascular function in patients with chronic heart failure

被引:0
作者
Kolwelter, Julie [1 ,2 ]
Bosch, Agnes [1 ]
Jung, Susanne [2 ]
Stabel, Lena [1 ]
Kannenkeril, Dennis [1 ]
Ott, Christian [1 ]
Bramlage, Peter [3 ]
Schiffer, Mario [1 ]
Achenbach, Stephan [2 ]
Schmieder, Roland E. [1 ]
机构
[1] Univ Hosp Erlangen, Friedrich Alexander Univ Erlangen Nuremberg FAU, Dept Hypertens & Nephrol, Ulmenweg 18, D-91054 Erlangen, Germany
[2] Univ Hosp Erlangen, Friedrich Alexander Univ Erlangen Nuremberg FAU, Dept Cardiol, Erlangen, Germany
[3] Inst Pharmacol & Prevent Med, Cloppenburg, Germany
来源
ESC HEART FAILURE | 2022年 / 8卷 / 06期
关键词
Chronic heart failure; Empagliflozin; SGLT2; inhibitor; Vascular function; Central haemodynamics; Blood pressure;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims Impairment of vascular function contributes to the progression of chronic heart failure (HF) by increasing the afterload. Treatment with selective sodium-glucose cotransporter 2 (SGLT2) inhibitors improves the prognosis of HF, but the precise mechanisms remain unclear. The aim of this study was to analyse the effect of empagliflozin on vascular function in patients with HF. Methods and results In an investigator initiated, double-blind, randomized, placebo-controlled, parallel-group, clinical study, patients with HF NYHA II-III and an ejection fraction of 49% or less were randomized 2:1 to receive empagliflozin 10 mg once daily or placebo for 3 months. A total of 74 patients (15% female), aged 66 +/- 9 years, with a mean ejection fraction of 39 +/- 8% and a median NTproBNP of 558 pg/mL (IQR 219-1051 pg/ml), were included. Vascular parameters such as central systolic blood pressure (cSBP), central pulse pressure (cPP), forward (FPH), and reflected pressure pulse height (RPH) decreased under resting conditions after 1 and 3 months (1 month: cSBP -6.4 +/- 8.3 mmHg, P < 0.001, cPP -3.0 +/- 6.6 mmHg, P = 0.004, FPH -2.5 +/- 4.5 mmHg, P = 0.001, RPH -1.6 +/- 3.0 mmHg, P = 0.001; 3 months: cSBP -4.6 +/- 8.4 mmHg, P = 0.001, cPP -3.1 +/- 4.8 mmHg, P < 0.001, FPH -1.7 +/- 3.7 mmHg, P = 0.004, RPH -1.4 +/- 2.5 mmHg, P = 0.001) in patients treated with empagliflozin (n = 45). In accordance, cSBP and cPP decreased in patients with empagliflozin treatment under 24 h ambulatory conditions after 1 and 3 months (1 month: cSBP -4.8 +/- 10.1 mmHg, P = 0.003, cPP -2.0 +/- 5.7 mmHg, P = 0.026; 3 months: cSBP -4.7 +/- 9.0 mmHg, P = 0.002, cPP -2.1 +/- 6.4 mmHg, P = 0.044). In the placebo group, there was no significant change after 1 and 3 months. The decrease in cSBP under resting conditions (-5.7 +/- 2.4 mmHg, P = 0.019) after 1 month and in cSBP (-6.0 +/- 2.6, P = 0.027) as well as in pulse wave velocity (-0.5 +/- 0.2 m/s, P = 0.021) under 24 h ambulatory conditions after 3 months was greater in the empagliflozin group than in the placebo group. Conclusions We found an improvement of vascular function after treatment with empagliflozin that indicates decreased afterload of the left ventricle and may contribute to the beneficial effects of SGLT2 inhibition in HF.
引用
收藏
页码:5327 / 5337
页数:11
相关论文
共 50 条
  • [21] Acute Effects of Preventing Heart Failure by Sodium-Glucose Cotransporter 2 Inhibitors
    Yanai, Hidekatsu
    CARDIOLOGY RESEARCH, 2021, 12 (05) : 324 - 326
  • [22] Tofogliflozin, a sodium-glucose cotransporter 2 inhibitor, improves pulmonary vascular remodeling due to left heart disease in mice
    Joki, Yusuke
    Konishi, Hakuoh
    Takasu, Kiyoshi
    Minamino, Tohru
    JOURNAL OF CARDIOLOGY, 2023, 81 (04) : 347 - 355
  • [23] Promising roles of sodium-glucose cotransporter 2 inhibitors in heart failure prevention and treatment
    Tanaka, Atsushi
    Node, Koichi
    DIABETOLOGY INTERNATIONAL, 2020, 11 (03) : 252 - 260
  • [24] Endothelial function and dysfunction: Impact of sodium-glucose cotransporter 2 inhibitors
    Ugusman, Azizah
    Kumar, Jaya
    Aminuddin, Amilia
    PHARMACOLOGY & THERAPEUTICS, 2021, 224
  • [25] Sodium-glucose cotransporter 2 inhibitors for the management of heart failure
    Nouel, Ana
    Winter, Jose Luis
    Sepulveda, Luis
    REVISTA MEDICA DE CHILE, 2022, 150 (12) : 1647 - 1654
  • [26] Heart failure prevention with sodium-glucose cotransporter 2 inhibitors
    Khan, Muhammad Shahzeb
    Butler, Javed
    JOURNAL OF DIABETES, 2019, 11 (07) : 601 - 604
  • [27] Genetic Variation in Sodium-glucose Cotransporter 2 and Heart Failure
    Katzmann, Julius L.
    Mason, Amy M.
    Marz, Winfried
    Kleber, Marcus E.
    Niessner, Alexander
    Bluher, Matthias
    Speer, Thimoteus
    Laufs, Ulrich
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2021, 110 (01) : 149 - 158
  • [28] Effects of Sodium-Glucose Cotransporter 2 Inhibitors for the Treatment of Patients With Heart Failure Proposal of a Novel Mechanism of Action
    Packer, Milton
    Anker, Stefan D.
    Butler, Javed
    Filippatos, Gerasimos
    Zannad, Faiez
    JAMA CARDIOLOGY, 2017, 2 (09) : 1025 - 1029
  • [29] Effect of sodium-glucose cotransporter 2 inhibitors on cardiac structure and function in type 2 diabetes mellitus patients with or without chronic heart failure: a meta-analysis
    Yu, Yi-Wen
    Zhao, Xue-Mei
    Wang, Yun-Hong
    Zhou, Qiong
    Huang, Yan
    Zhai, Mei
    Zhang, Jian
    CARDIOVASCULAR DIABETOLOGY, 2021, 20 (01)
  • [30] Empagliflozin, a sodium-glucose cotransporter inhibitor enhancing mitochondrial action and cardioprotection in metabolic syndrome
    Li, Yunhao
    Zhang, Zhanming
    Zhang, Zheming
    Zheng, Ningning
    Ding, Xudong
    JOURNAL OF CELLULAR PHYSIOLOGY, 2024, 239 (06)