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Increased bone resorption is associated with increased risk of cardiovascular events in men: the MINOS study
Pawel Szulc1, Elizabeth J Samelson, Douglas P Kiel
1INSERM Research Unit 831 and University of Lyon, Lyon, France. pawel.szulc@inserm.fr
Insights
Older men with low bone density or high bone resorption face double the risk of heart attack and stroke. Osteoporosis screening may benefit cardiovascular health in men.
Area of Science:
- Gerontology
- Cardiology
- Endocrinology
Background:
- Cardiovascular disease and osteoporosis are prevalent in aging men.
- Shared underlying mechanisms may link bone and vascular health.
Purpose of the Study:
- To investigate the association between bone mineral density (BMD), bone turnover markers (BTMs), and cardiovascular events in men aged 50 and older.
Main Methods:
- Prospective study of 744 men (age >=50) over 7.5 years.
- Assessed BMD (spine, whole body, forearm) and BTMs (bone resorption markers).
- Analyzed risk of myocardial infarction and stroke, adjusting for confounders.
Main Results:
- Low BMD (lowest quartile) was associated with a 2-fold increased risk of cardiovascular events.
- High bone resorption markers (highest quartile) also showed a 2-fold increased risk of cardiovascular events.
- Findings remained significant after adjusting for confounders and prevalent cardiovascular disease.
Conclusions:
- Low bone mineral density and high bone resorption indicate increased risk for myocardial infarction and stroke in older men.
- Men diagnosed with osteoporosis may warrant cardiovascular disease screening.
- Further research into shared biological pathways is needed to identify at-risk individuals and develop treatments.
Abstract:
Better assessment of the association between cardiovascular disease and osteoporosis in older men may help identify shared etiologies for bone and heart health in this population. We assessed the association of BMD and bone turnover markers (BTMs) with risk of cardiovascular events (myocardial infarction or stroke) in 744 men >or=50 yr of age. During the 7.5-yr prospective follow-up, 43 strokes and 40 myocardial infarctions occurred in 79 men. After adjustment for confounders (age, weight, height, smoking, education, physical activity, self-reported history of diabetes, hypertension, and prevalent ischemic heart disease), men in the lowest quartile of BMD at the spine, whole body, and forearm had a 2-fold increased risk of cardiovascular events. Men in the highest quartile of bone resorption markers (deoxypyridinoline [DPD], C-telopeptide of type I collagen) had a 2-fold increased risk of cardiovascular events (e.g., multivariable-adjusted hazard ratio [including additional adjustment for BMD] was 2.11 [95% CI: 1.26-3.56], for the highest quartile of free DPD relative to the lowest three quartiles). The results were similar for men without prevalent ischemic heart disease and for myocardial infarction and stroke analyzed separately. Our data suggest that men with low BMD or high bone resorption may be at increased risk of myocardial infarction and stroke in addition to fracture. Thus, men with osteoporosis may benefit from screening for cardiovascular disease. Further study to elucidate the biological mechanism shared by bone and vascular disease may help efforts to identify men at risk or develop treatment.
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