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Relation between bone mineral density, bone loss and the risk of cardiovascular disease in a Chinese cohort
Cheng Shen1, Juan Deng, Rui Zhou
1Department of Cardiovascular Surgery, Daping Hospital, Third Military Medical University, Chongqing, China.
Insights
Low bone mineral density (BMD) and rapid bone loss increase cardiovascular disease (CVD) risk. Lifestyle factors like smoking and drinking also elevate CVD risk, while adiponectin may offer protection.
Area of Science:
- Gerontology
- Cardiology
- Endocrinology
Background:
- Cardiovascular disease (CVD) and osteoporosis share risk factors like aging, smoking, and hypertension.
- Previous research on bone mineral density (BMD) and CVD risk yields conflicting results.
- Limited data exists on the association between BMD loss rate and CVD incidence.
Purpose of the Study:
- To investigate the relationship between BMD, bone loss rate, and CVD risk over five years.
- To analyze these associations within a Chinese cohort.
Main Methods:
- A 5-year prospective study involving 6,092 Chinese adults aged 30-75.
- Collected baseline data on demographics, BMD, lifestyle, medical history, and blood markers.
- Utilized Cox proportional hazards analysis to assess BMD and CVD incidence.
Main Results:
- Over five years, 118 subjects developed CVD.
- Baseline BMD, bone loss rate, smoking, and alcohol consumption were independent predictors of increased CVD risk.
- Elevated osteoprotegerin and leptin levels correlated with higher CVD risk, while higher adiponectin levels were associated with decreased CVD risk.
Conclusions:
- Bone health and cardiovascular health are interconnected.
- Understanding the link between osteoporosis and CVD is crucial for elucidating their shared pathogenesis.
- BMD and bone loss rate are significant indicators for cardiovascular risk assessment.
Abstract:
Cardiovascular disease (CVD) and osteoporosis share some common risk factors such as old age, smoking, alcoholic drinking, hypertension, diabetes mellitus, and hyperlipidemia. Although previous studies have investigated the association of bone mineral density (BMD) with CVD, the results were conflicting. There are limited studies on the association of BMD loss rate with CVD. We therefore conducted a 5-year prospective study to examine the relation among BMD, bone loss, and risk of CVD in a Chinese cohort. Of 9,657 community residents 30 to 75 years old, 6,092 were enrolled in the study and followed annually for 5 years. At baseline demographic data, BMD, smoking and drinking statuses, medical history, and blood samples were collected. Cox proportional hazards analysis was used to evaluate the association of BMD and incidence of CVD. Over the 5-year follow-up period, CVD developed in 118 subjects. Baseline BMD, bone loss rate, current smoking, daily alcoholic ingestion, and higher osteoprotegerin and leptin levels were independently associated with increased risk of CVD, whereas higher baseline adiponectin level was associated with decreased risk of CVD in women and men. In conclusion, uncovering the relation linking osteoporosis and CVD is important for understanding the pathogenesis of these 2 common disorders.
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