GLP-1 receptor agonists and myocardial metabolism in atrial fibrillation

被引:1
|
作者
Zhong, Jiani [1 ,2 ]
Chen, Hang [1 ,2 ]
Liu, Qiming [1 ]
Zhou, Shenghua [1 ]
Liu, Zhenguo [3 ,4 ]
Xiao, Yichao [1 ]
机构
[1] Cent South Univ, Xiangya Hosp 2, Dept Cardiovasc Med, Changsha 410011, Peoples R China
[2] Cent South Univ, Xiangya Sch Med, Changsha 410008, Peoples R China
[3] Univ Missouri, Ctr Precis Med, Columbia, MO 65211 USA
[4] Univ Missouri, Sch Med, Dept Med, Div Cardiovasc Med, Columbia, MO 65211 USA
关键词
Atrial fibrillation; Glucagon-like peptide-1 receptor agonists; Metabolism; GLUCAGON-LIKE PEPTIDE-1; HEART-FAILURE; CARDIOVASCULAR OUTCOMES; CARDIAC-HYPERTROPHY; REPERFUSION INJURY; ENDOTHELIAL-CELLS; OXIDATIVE STRESS; GLUCOSE-UPTAKE; DOUBLE-BLIND; EXENDIN-4;
D O I
10.1016/j.jpha.2023.12.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Atrial fibrillation (AF) is the most common cardiac arrhythmia. Many medical conditions, including hypertension, diabetes, obesity, sleep apnea, and heart failure (HF), increase the risk for AF. Cardiomyocytes have unique metabolic characteristics to maintain adenosine triphosphate production. Significant changes occur in myocardial metabolism in AF. Glucagon-like peptide-1 receptor agonists (GLP-1RAs) have been used to control blood glucose fluctuations and weight in the treatment of type 2 diabetes mellitus (T2DM) and obesity. GLP-1RAs have also been shown to reduce oxidative stress, inflammation, autonomic nervous system modulation, and mitochondrial function. This article reviews the changes in metabolic characteristics in cardiomyocytes in AF. Although the clinical trial outcomes are unsatisfactory, the findings demonstrate that GLP-1 RAs can improve myocardial metabolism in the presence of various risk factors, lowering the incidence of AF. (c) 2023 The Author(s). Published by Elsevier B.V. on behalf of Xi'an Jiaotong University. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
下载
收藏
页数:13
相关论文
共 50 条
  • [1] GLP-1 RECEPTOR AGONISTS AND CARDIOVASCULAR OUTCOMES IN PATIENTS WITH ATRIAL FIBRILLATION AND DIABETES
    Rangavajla, Gautam
    Ayub, Muhammad Talha
    Thoma, Floyd
    Mulukutla, Suresh
    Zhu, Jianhui
    Jain, Sandeep K.
    Saba, Samir F.
    Bhonsale, Aditya
    JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2024, 83 (13) : 192 - 192
  • [2] GLP-1 receptor agonists and the risk of atrial fibrillation: a real-world evidence
    Shin, J. I.
    Xu, Y.
    Boyle, T.
    Lyu, B.
    Ballew, S.
    Selvin, E.
    Chang, A.
    Inker, L.
    Grams, M.
    DIABETES RESEARCH AND CLINICAL PRACTICE, 2023, 197
  • [3] GLP-1 receptor agonists in NAFLD
    Petit, J. -M.
    Verges, B.
    DIABETES & METABOLISM, 2017, 43 : 2S28 - 2S33
  • [4] Emerging GLP-1 receptor agonists
    Lund, Asger
    Knop, Filip K.
    Vilsboll, Tina
    EXPERT OPINION ON EMERGING DRUGS, 2011, 16 (04) : 607 - 618
  • [5] GLP-1 receptor agonists today
    Marre, Michel
    Penfornis, Alfred
    DIABETES RESEARCH AND CLINICAL PRACTICE, 2011, 93 (03) : 317 - 327
  • [6] The Future of the GLP-1 Receptor Agonists
    Hirsch, Irl B.
    JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2019, 321 (15): : 1457 - 1458
  • [7] Positioning on GLP-1 receptor agonists
    Gimenez, Sergio
    Piskorz, Daniel
    Martinez Demaria, Diego
    Nanfara, Silvia
    Lorenzatti, Alberto
    Zapata, Gerardo
    Aguinaga Arrascue, Luis
    Perna, Eduardo
    REVISTA DE LA FEDERACION ARGENTINA DE CARDIOLOGIA, 2021, 50 : 4 - 10
  • [8] GLP-1 Receptor Agonists, the Holy Grail Preventing Atrial Fibrillation in Patients With T2D?
    Stoll, Lisa
    Lo, James C.
    JACC-BASIC TO TRANSLATIONAL SCIENCE, 2023, 8 (08): : 937 - 938
  • [9] Future Perspectives on GLP-1 Receptor Agonists and GLP-1/glucagon Receptor Co-agonists in the Treatment of NAFLD
    Seghieri, Marta
    Christensen, Alexander S.
    Andersen, Andreas
    Solini, Anna
    Knop, Filip K.
    Vilsboll, Tina
    FRONTIERS IN ENDOCRINOLOGY, 2018, 9
  • [10] The Cardiovascular Effects of GLP-1 Receptor Agonists
    Okerson, Theodore
    Chilton, Robert J.
    CARDIOVASCULAR THERAPEUTICS, 2012, 30 (03) : e146 - e155