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Associations of Biological Age and Heart Age Accelerations With New-Onset Stroke in Individuals With
Hao Zhu1, Hannah Lui1, Li He2
1Department of Paediatrics and Adolescent Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
Insights
Biological age acceleration and heart age acceleration are linked to increased stroke risk in individuals with cardiovascular-kidney-metabolic (CKM) syndrome. Men with accelerated heart age are particularly vulnerable, highlighting potential new risk stratification tools.
Area of Science:
- Cardiovascular Medicine
- Gerontology
- Public Health
Background:
- Cardiovascular-kidney-metabolic (CKM) syndrome presents a significant stroke risk.
- Current risk stratification indicators for stroke in CKM syndrome are limited.
- Biological age and heart age acceleration are emerging markers of physiological aging.
Purpose of the Study:
- To investigate the association between biological age acceleration (BioAge-gap) and heart age acceleration (HeartAge-gap) with new-onset stroke in CKM syndrome.
- To identify effective risk stratification indicators for stroke prevention in CKM syndrome patients.
- To explore potential gender-specific differences in stroke risk related to accelerated aging.
Main Methods:
- Prospective cohort study using data from the China Health and Retirement Longitudinal Study (CHARLS) (2015-2020).
- Calculation of BioAge-gap using the Klemera-Doubal method and HeartAge-gap using the Framingham risk score.
- Analysis of 7283 participants (aged 45-75) with physician-diagnosed stroke as the primary outcome.
Main Results:
- Biological age acceleration (BioAge-gap) was positively associated with new-onset stroke (OR = 1.05, p < 0.01).
- Accelerated heart age (HeartAge-gap ≥ 0 years) significantly increased stroke risk (74% for 0-5 years, 141% for ≥5 years).
- A significant gender interaction was observed, with men showing higher vulnerability to stroke with accelerated heart age.
Conclusions:
- Biological age acceleration and heart age acceleration are significant predictors of new-onset stroke in individuals with CKM syndrome.
- These intuitive aging metrics can enhance stroke risk stratification and primary prevention strategies.
- Targeted interventions for men with accelerated heart age may be crucial for mitigating stroke risk in CKM syndrome.
Abstract:
Individuals with cardiovascular-kidney-metabolic (CKM) syndrome face an elevated risk of stroke, yet effective risk stratification indicators remain limited. This prospective study aims to investigate the associations of biological age acceleration (BioAge-gap) and heart age acceleration (HeartAge-gap) with new-onset stroke in individuals with CKM syndrome Stages 0-3, utilizing data from the China Health and Retirement Longitudinal Study (CHARLS) collected between 2015 and 2020. Baseline BioAge-gap and HeartAge-gap were calculated via the Klemera-Doubal method (KDM) and Framingham risk score (FRS), respectively. The primary outcome was self-reported physician-diagnosed stroke identified during the 2018 and 2020 follow-ups. Analysis of 7283 eligible participants aged 45-75 years revealed a positive association between BioAge-gap and new-onset stroke (odds ratio [OR] = 1.05, p < 0.01). Furthermore, compared to participants with a non-positive HeartAge-gap, those with HeartAge-gaps of 0-5 years and ≥5 years exhibited significantly increased risks of stroke by 74% and 141%, respectively. Subgroup analyses and interaction tests identified a significant gender interaction in the association between HeartAge-gap and stroke, indicating that men with accelerated heart age represent a vulnerable subgroup. Restricted cubic splines (RCSs) confirmed a linear association, and sensitivity analyses validated the robustness of these findings. Integrating these intuitive indicators into clinical practice could facilitate primary stroke prevention and mitigate CKM syndrome progression.
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