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Published on: November 5, 2016
Age and Human Regenerative Capacity Impact of Cardiovascular Risk Factors
Ibhar Al Mheid1, Salim S Hayek1, Yi-An Ko1
1From the Division of Cardiology, Emory Clinical Cardiovascular Research Institute, Emory-Georgia Tech, Predictive Health Institute, Atlanta, GA.
Healthy aging does not decrease circulating progenitor cells (PCs). However, cardiovascular disease risk factors initially boost PCs in younger individuals but lower them in older adults, impacting regenerative capacity.
Area of Science:
- Cardiovascular health
- Regenerative medicine
- Aging research
Background:
- Human endogenous reparative capacity and its association with aging, cardiovascular disease (CVD), and risk factors (RFs) remain unclear.
- Circulating progenitor cells (PCs) are key indicators of regenerative potential.
- The impact of RFs and CVD on PC levels during aging requires investigation.
Purpose of the Study:
- To investigate the aging of endogenous reparative capacity.
- To determine if cardiovascular disease or its risk factors affect reparative capacity.
- To examine the effect of healthy aging versus aging with RFs or CVD on circulating progenitor cell (PC) levels.
Main Methods:
- Analyzed data from 2792 adult subjects categorized by RFs and CVD status.
- Enumerated PCs using flow cytometry, identifying specific cell surface markers.
- Utilized multivariable adjustment to assess associations between age, RFs, CVD, and PC counts.
Main Results:
- PC counts were higher in younger individuals, males, and those with larger body size.
- Both increasing age and higher RF/CVD burden were independently associated with lower PC counts.
- PC counts remained stable with age in healthy individuals, but interactions showed RFs increased PCs in younger subjects and decreased them in older subjects.
Conclusions:
- Circulating PC levels do not decline during healthy aging.
- RF exposure initially stimulates PC mobilization in younger individuals.
- Continued RF/CVD exposure is linked to reduced PC levels in later life, indicating an overall decline in regenerative capacity over the lifespan.
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