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Accelerated biological aging: unveiling the path to cardiometabolic multimorbidity, dementia, and mortality
1Department of Neurology, Chengdu Seventh People's Hospital, Chengdu, China.
Insights
Accelerated biological aging significantly increases the risk of cardiometabolic multimorbidity (CMM), dementia, and mortality. Maintaining healthy cardiovascular metrics may help counteract age acceleration and its adverse health outcomes.
Area of Science:
- Gerontology
- Cardiovascular Medicine
- Epidemiology
Background:
- Cardiometabolic multimorbidity (CMM) and aging are significant public health challenges.
- CMM involves the coexistence of multiple cardiometabolic diseases (CMD) such as stroke, ischemic heart disease, and diabetes.
Purpose of the Study:
- To investigate the association between biological aging and the progression of CMM towards dementia and mortality.
- To examine the role of accelerated biological aging in the development of cardiometabolic diseases and their long-term health consequences.
Main Methods:
- Utilized the UK Biobank cohort, including 415,147 individuals.
- Calculated biological age using KDM-BA and PhenoAge algorithms to identify accelerated aging.
- Employed fully-adjusted Cox regression models to analyze risks over an 11-year follow-up period.
Main Results:
- Accelerated aging was linked to significantly higher risks of developing CMD, CMM, dementia, and mortality.
- Individuals with accelerated aging showed increased hazard ratios for CMM, dementia, and mortality, both from a CMD-free state and with existing CMD.
- Cardiometabolic multimorbidity partially mediated the effect of accelerated aging on dementia and mortality.
Conclusions:
- Biological aging encompasses the progression from cardiometabolic disease-free status to CMM, dementia, and death.
- The Life's Essential 8 score presents a potential target for interventions aimed at mitigating age acceleration and its associated health risks.
Background:
Cardiometabolic multimorbidity (CMM) and aging are increasing public health concerns. This prospective study used UK Biobank cohort to investigate the relationship between biological aging and the trajectory of CMM to dementia and mortality.
Methods:
CMM is the coexistence of at least two cardiometabolic diseases (CMD), including stroke, ischemic heart disease, and diabetes. Biological age was calculated using the KDM-BA and PhenoAge algorithms. Accelerated aging indicated biological age advances more rapidly than chronological age.
Results:
The study included 415,147 individuals with an average age of 56.5 years. During the average 11-year follow-up period, CMD-free individuals with accelerated aging had a significantly greater risk of CMD (KDM-BA, HR 1.456; PhenoAge, HR 1.404), CMM (KDM-BA, HR 1.952; PhenoAge, HR 1.738), dementia (KDM-BA, HR 1.243; PhenoAge, HR 1.212), and mortality (KDM-BA, HR 1.821; PhenoAge, HR 2.047) in fully-adjusted Cox regression models (p < 0.05 for all). Accelerated aging had adjusted HRs of 1.489 (KDM-BA) and 1.488 (PhenoAge) for CMM, 1.434 (KDM-BA) and 1.514 (PhenoAge) for dementia, and 1.943 (KDM-BA) and 2.239 (PhenoAge) for mortality in participants with CMD at baseline (p < 0.05 for all). CMM significantly mediated accelerated aging's indirect effects on dementia by 13.7% (KDM-BA, HR) and 21.6% (PhenoAge); those on mortality were 4.7% (KDM-BA) and 5.2% (PhenoAge). The population attributable-risk of Life's Essential 8 score (≥80 vs. <80) were 0.79 and 0.43 for KDM-BA and PhenoAge accelerated aging, respectively.
Conclusion:
Biological aging involves the entire trajectory of CMM from a CMD-free state to CMD, to CMM, and ultimately to dementia and death. Life's Essential 8 may be a potential target to counter age acceleration.
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