Hallmarks of cardiovascular ageing

Mahmoud Abdellatif1,2,3,4, Peter P Rainer5,6, Simon Sedej5,6,7

  • 1Department of Cardiology, Medical University of Graz, Graz, Austria. mahmoud.abdellatif@medunigraz.at.

Insights

Cardiovascular aging is driven by eight molecular hallmarks, including inflammation and cell senescence. Targeting these hallmarks may reduce age-related cardiovascular disease risk.

Area of Science:

  • Cardiovascular biology and aging research.

Background:

  • Cardiovascular diseases are a leading cause of mortality and morbidity worldwide.
  • Maintaining cardiovascular health is crucial for promoting both organismal healthspan and lifespan.
  • Cardiovascular aging may precede or underlie age-related health deterioration.

Purpose of the Study:

  • To identify common molecular hallmarks of cardiovascular aging.
  • To propose a hierarchical order for these hallmarks.
  • To discuss therapeutic strategies targeting these hallmarks to reduce cardiovascular risk in older individuals.

Main Methods:

  • This review synthesizes current research on molecular mechanisms of cardiovascular aging.
  • It proposes a framework of eight common molecular hallmarks.
  • It discusses potential therapeutic interventions based on these hallmarks.

Main Results:

  • Eight molecular hallmarks common to cardiovascular aging are identified: disabled macroautophagy, loss of proteostasis, genomic instability (including clonal hematopoiesis of indeterminate potential), epigenetic alterations, mitochondrial dysfunction, cell senescence, dysregulated neurohormonal signaling, and inflammation.
  • A hierarchical order distinguishing primary (upstream) from antagonistic and integrative (downstream) hallmarks is proposed.
  • Therapeutic targeting of these hallmarks is discussed as a strategy to attenuate residual cardiovascular risk.

Conclusions:

  • Cardiovascular aging is characterized by eight interconnected molecular hallmarks.
  • Understanding the hierarchy of these hallmarks is crucial for developing effective interventions.
  • Targeting these hallmarks offers potential therapeutic avenues to improve cardiovascular healthspan and lifespan in aging populations.

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