Heart Disease and Ageing: The Roles of Senescence, Mitochondria, and Telomerase in Cardiovascular Disease

Subcell Biochem. 2023:103:45-78. doi: 10.1007/978-3-031-26576-1_4.

Abstract

During ageing molecular damage leads to the accumulation of several hallmarks of ageing including mitochondrial dysfunction, cellular senescence, genetic instability and chronic inflammation, which contribute to the development and progression of ageing-associated diseases including cardiovascular disease. Consequently, understanding how these hallmarks of biological ageing interact with the cardiovascular system and each other is fundamental to the pursuit of improving cardiovascular health globally. This review provides an overview of our current understanding of how candidate hallmarks contribute to cardiovascular diseases such as atherosclerosis, coronary artery disease and subsequent myocardial infarction, and age-related heart failure. Further, we consider the evidence that, even in the absence of chronological age, acute cellular stress leading to accelerated biological ageing expedites cardiovascular dysfunction and impacts on cardiovascular health. Finally, we consider the opportunities that modulating hallmarks of ageing offer for the development of novel cardiovascular therapeutics.

Keywords: Ageing; Atherosclerosis; Cardiovascular; Heart failure; Inflammation; Remodelling; Senescence; Senolytic.

Publication types

  • Review

MeSH terms

  • Aging / genetics
  • Cardiovascular Diseases* / genetics
  • Cellular Senescence
  • Heart Diseases*
  • Humans
  • Mitochondria / genetics
  • Telomerase* / genetics

Substances

  • Telomerase