Cited by 67Cardiac Ischemia and ReperfusionCardiac Fibrosis and RemodelingCardiovascular Function and Risk Factors

Cardiomyocyte ageing and cardioprotection: consensus document from the ESC working groups cell biology of the heart and myocardial function

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Ruiz-Meana, Marisol, Bou-Teen, Diana, Ferdinandy, Péter, Gyongyosi, Mariann, Pesce, Maurizio, Perrino, Cinzia, Schulz, Rainer, Sluijter, Joost P G +3 more·2020·Cardiovascular Research

Abstract

Advanced age is a major predisposing risk factor for the incidence of coronary syndromes and comorbid conditions which impact the heart response to cardioprotective interventions. Advanced age also significantly increases the risk of developing post-ischaemic adverse remodelling and heart failure after ischaemia/reperfusion (IR) injury. Some of the signalling pathways become defective or attenuated during ageing, whereas others with well-known detrimental consequences, such as glycoxidation or proinflammatory pathways, are exacerbated. The causative mechanisms responsible for all these changes are yet to be elucidated and are a matter of active research. Here, we review the current knowledge about the pathophysiology of cardiac ageing that eventually impacts on the increased susceptibility of cells to IR injury and can affect the efficiency of cardioprotective strategies.

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  • Because mature cardiomyocytes have a low proliferation rate, the injured area in the aging heart is replaced by fibrotic scar tissue, resulting in organ failure.

    “In addition, because mature cardiomyocytes have a low rate of proliferation, the injured area in the aging heart is replaced by fibrotic scar tissue, resulting in organ failure.141”

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Research works printed but not linked: 3

  1. Paneni F, Diaz Canestro C, Libby P, Luscher TF, Camici GG. The aging cardiovascu- lar system: understanding it at the cellular and clinical levels. J Am Coll Cardiol 2017; 69:1952-1967.
  2. Zhu B, Zhang L, Liang C, Liu B, Pan X, Wang Y, Zhang Y, Zhang Y, Xie W, Yan B, Liu F, Yip H-K, Yu X-y, Li Y. Stem cell-derived exosomes prevent aging-induced car- diac dysfunction through a novel exosome/lncRNA MALAT1/NF-kappaB/TNF-alpha signaling pathway. Oxid Med Cell Longev 2019;2019:1-14.
  3. Wang X-X, Wang X-L, Tong M-M, Gan L, Chen H, Wu S-S, Chen J-X, Li R-L, Wu Y, Zhang H-y, Zhu Y, Li Y-X, He J-h, Wang M, Jiang W. SIRT6 protects cardiomyo- cytes against ischemia/reperfusion injury by augmenting FoxO3alpha-dependent an- tioxidant defense mechanisms. Basic Res Cardiol 2016;111:13.

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Authors
Ruiz-Meana, M., Bou-Teen, D., Ferdinandy, P., Gyongyosi, M., Pesce, M., Perrino, C., Schulz, R., Sluijter, J. P. G., Tocchetti, C. G., Thum, T., & Madonna, R.
Affiliations
  • Department of Cardiology, Hospital Universitari Vall d’Hebron, Vall d’Hebron Institut de Recerca (VHIR), Universitat Autonoma de Barcelona and Centro de Investigación Biomédica en Red-CV, CIBER-CV , Madrid,
  • Semmelweis University (HU)
  • Department of Cardiology, Medical University of Vienna , Waehringer Guertel 18-20, A-1090 Vienna,
  • Centro Cardiologico Monzino (IT)
  • Federico II University Hospital (IT)
  • Justus-Liebig-Universität Gießen (DE)
  • Utrecht University (NL)
  • Medizinische Hochschule Hannover (DE)
  • University of Pisa (IT)
Corresponding author
Madonna, Rosalinda
Venue
Cardiovascular Research
Published
2020-05-08
Volume
116
Issue
11
Pages
1835-1849
ISSN
  • 0008-6363 (ISSN-L)
  • 1755-3245
OpenAlex
W3023592989
Cited by
67
References
158
Citations by year
2026: 11 · 2025: 12 · 2024: 9 · 2023: 11 · 2022: 13 · 2021: 7 · 2020: 4
FWCI
5.75
Type
journal article
Language
en
Open access
Locations
  • Cardiovascular Research (publishedVersion)
  • PubMed (publishedVersion)
  • CINECA IRIS Institutial research information system (University of Pisa) (submittedVersion)
  • Utrecht University Repository (Utrecht University) (submittedVersion, other-oa)
Funders
  • COST Action EU-CARDIOPROTECTION (CA16225)
  • COST
  • European Cooperation in Science and Technology
  • ISCIII (PI19-01196)
  • European Regional Development Fundings
  • Federico II University
  • Ricerca di Ateneo
  • Incyte s.r.l. and from Ministero dell’Istruzione
  • Università e Ricerca Scientifica (549901_2020)
  • National Research, Development and Innovation Office of Hungary
  • National Heart Program (NVKP 16-1-2016-0017)
  • Higher Education Institutional Excellence Program
  • Ministry of Human Capacities in Hungary
  • Therapeutic Devepment
  • Semmelweis University
Topics
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Cardiac Ischemia and Reperfusion
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac Fibrosis and Remodeling
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Function and Risk Factors
Keywords
cardiac aging, cardiomyocytes, cardioprotection, ischemia-reperfusion injury, heart failure, glycoxidation, inflammation, signaling pathways, coronary syndrome, old age
MeSH terms
Heart Disease Risk Factors, Age Factors, Aging, Animals, Disease Models, Animal, Extracellular Matrix, Heart Diseases, Humans, Phenotype, Prognosis, Cellular Senescence, Risk Assessment, Myocytes, Cardiac

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