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Assessment of Vascular Tone Responsiveness using Isolated Mesenteric Arteries with a Focus on Modulation by Perivascular Adipose Tissues
Published on: June 3, 2019
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.
Abstract:
Normal circulatory function is a key determinant of disease-free life expectancy (healthspan). Indeed, pathologies affecting the cardiovascular system, which are growing in prevalence, are the leading cause of global morbidity, disability and mortality, whereas the maintenance of cardiovascular health is necessary to promote both organismal healthspan and lifespan. Therefore, cardiovascular ageing might precede or even underlie body-wide, age-related health deterioration. In this Review, we posit that eight molecular hallmarks are common denominators in cardiovascular ageing, namely disabled macroautophagy, loss of proteostasis, genomic instability (in particular, clonal haematopoiesis of indeterminate potential), epigenetic alterations, mitochondrial dysfunction, cell senescence, dysregulated neurohormonal signalling and inflammation. We also propose a hierarchical order that distinguishes primary (upstream) from antagonistic and integrative (downstream) hallmarks of cardiovascular ageing. Finally, we discuss how targeting each of the eight hallmarks might be therapeutically exploited to attenuate residual cardiovascular risk in older individuals.
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