TY - JOUR
T1 - Senescence-related myocardial dysfunction
T2 - Keeping a young heart
AU - Ajjan, Ramzi A
AU - Huckstepp, Robert T R
AU - Akbar, Naveed
AU - Bauersachs, Johann
AU - Lok, Jesher Ching Wai
AU - Choppy-Madeleine, Juel
AU - Christopher, Gary
AU - Dalakoti, Mayank
AU - Dawson-Plincke, Emily
AU - Dodds, John
AU - Ellison-Hughes, Georgina M
AU - Emanueli, Costanza
AU - George, Christopher H
AU - Goyal, Anushka
AU - Higginbotham, Victoria
AU - Holzner, Lorenz
AU - Kanamarlapudi, Venkateswarlu
AU - Madeddu, Paolo
AU - Mauro, Claudio
AU - Lewis-McDougall, Fiona
AU - Murray, Andrew J
AU - Damien Genetus, Renita Peter
AU - Short, Emma
AU - Sussman, Mark A
AU - Tavares, Adriana A S
AU - Thompson, Samuel
AU - Wadodkar, Morya
AU - Calimport, Stuart R G
AU - Bentley, Barry L
PY - 2026/3/6
Y1 - 2026/3/6
N2 - The heart, a vital organ, works without interruption and constantly adjusts to the ever-changing demands on our body. It adapts to physiological and pathological changes, including exercise and emotional state, as well as metabolic, respiratory, and vascular abnormalities. The pumping action of the heart is determined by the health of the myocardium, which undergoes changes with ageing that are both under-investigated and incompletely understood, potentially impacting our approach to pathological conditions. Here, the alterations in cellular, tissue, and gross physiological function of the heart with age are discussed. At the molecular level, non-coding RNAs influence cellular senescence, and extracellular vesicles induce fibrosis through matrix remodelling. Mitochondrial dysfunction and altered fatty acid oxidation reduce cellular energetics, whilst accumulation of reactive oxygen species and steatosis, as well as telomere shortening coupled with reduced autophagy, limit the myocardium’s regenerative capability. Loss of cardiomyocytes, combined with senescence, requires compensatory hypertrophy, inducing myocardial stiffness and altered muscle function. In addition to these direct alterations in myocardial characteristics with ageing, other factors that can affect the myocardium indirectly are addressed, including valve calcification, resulting in regurgitation and/or stenosis; vascular abnormalities, reducing compliance and exacerbating hypertension; fibrosis leading to cardiac arrhythmias; and autonomic dysregulation, reducing cardiac adaptability. Finally, potential modulation of cardiac ageing is discussed whilst also addressing which senescent modifications should be considered as ageing-related physiological changes of the myocardium. A better understanding of myocardial ageing will differentiate physiological changes from early, preventable, and reversible pathological changes, consequently helping to optimize management of individuals with or at risk of myocardial disease by taking into account diverse trajectories of myocardial ageing.
AB - The heart, a vital organ, works without interruption and constantly adjusts to the ever-changing demands on our body. It adapts to physiological and pathological changes, including exercise and emotional state, as well as metabolic, respiratory, and vascular abnormalities. The pumping action of the heart is determined by the health of the myocardium, which undergoes changes with ageing that are both under-investigated and incompletely understood, potentially impacting our approach to pathological conditions. Here, the alterations in cellular, tissue, and gross physiological function of the heart with age are discussed. At the molecular level, non-coding RNAs influence cellular senescence, and extracellular vesicles induce fibrosis through matrix remodelling. Mitochondrial dysfunction and altered fatty acid oxidation reduce cellular energetics, whilst accumulation of reactive oxygen species and steatosis, as well as telomere shortening coupled with reduced autophagy, limit the myocardium’s regenerative capability. Loss of cardiomyocytes, combined with senescence, requires compensatory hypertrophy, inducing myocardial stiffness and altered muscle function. In addition to these direct alterations in myocardial characteristics with ageing, other factors that can affect the myocardium indirectly are addressed, including valve calcification, resulting in regurgitation and/or stenosis; vascular abnormalities, reducing compliance and exacerbating hypertension; fibrosis leading to cardiac arrhythmias; and autonomic dysregulation, reducing cardiac adaptability. Finally, potential modulation of cardiac ageing is discussed whilst also addressing which senescent modifications should be considered as ageing-related physiological changes of the myocardium. A better understanding of myocardial ageing will differentiate physiological changes from early, preventable, and reversible pathological changes, consequently helping to optimize management of individuals with or at risk of myocardial disease by taking into account diverse trajectories of myocardial ageing.
U2 - 10.1093/eurheartj/ehag095
DO - 10.1093/eurheartj/ehag095
M3 - Article
SN - 0195-668X
JO - European Heart Journal
JF - European Heart Journal
ER -