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Osteoporosis and cardiac remodeling in middle-aged and older adults: a cross-sectional study
Haoran Wang1, Qichao Wang2, Bing He3
1Cardiovascular Institute of Luohe, Luohe Central Hospital, Luohe Medical College, Luohe, 462003, China. washingtonhr@163.com.
Insights
Lower bone mineral density (BMD) is linked to cardiac changes like left atrial enlargement and thicker heart walls. These findings in osteoporosis patients suggest shared pathways between bone loss and cardiovascular remodeling.
Area of Science:
- Cardiovascular Medicine
- Bone Metabolism
- Gerontology
Background:
- Osteoporosis and cardiovascular disease (CVD) are prevalent, particularly in aging populations.
- The intricate relationship between bone mineral density (BMD) and cardiac structure/function requires further elucidation.
Purpose of the Study:
- To investigate the association between BMD and cardiac parameters in a cohort study.
- To identify potential shared pathophysiological mechanisms linking bone loss and cardiac remodeling.
Main Methods:
- Cross-sectional analysis of 1233 participants from the Osteoarthritis and Cardiovascular Health Cohort.
- BMD assessed using T-scores and categorized into normal, osteopenia, and osteoporosis.
- Cardiac structure and function evaluated via echocardiography, measuring parameters like left atrial volume index (LAVI) and relative wall thickness (RWT).
- Multivariable linear regression models adjusted for age, sex, and cardiovascular risk factors.
Main Results:
- Osteoporosis was associated with significantly higher LAVI and RWT compared to normal BMD.
- Lower BMD (T-score) was independently and inversely associated with LAVI and RWT after multivariable adjustment.
- These associations were more pronounced in women and in participants under 50 years of age.
- No significant associations were found with left ventricular mass index, ejection fraction, or diastolic function.
Conclusions:
- Reduced BMD is independently associated with left atrial enlargement and increased cardiac ventricular wall thickness.
- These findings suggest shared underlying mechanisms contributing to both bone loss and cardiac remodeling.
- Further research is warranted to explore these interconnected pathophysiological pathways.
Abstract:
Osteoporosis is associated with cardiovascular disease, but the relationship between bone mineral density (BMD) and cardiac structure and function remains incompletely understood. This cross-sectional study analyzed baseline data from 1233 participants (median age 60 years; 59% female) in the Osteoarthritis and Cardiovascular Health Cohort. BMD was categorized as normal (T-score ≥ - 1.0, n = 364), osteopenia (- 2.5 < T-score < - 1.0, n = 404), or osteoporosis (T-score ≤ - 2.5, n = 465). Cardiac parameters were measured via echocardiography. Multivariable linear regression adjusted for age, sex, and cardiovascular risk factors. Osteoporosis was associated with higher LAVI (median: 29 vs. 26 mL/m2, P < 0.001) and RWT (0.38 vs. 0.37, P = 0.047) compared to normal BMD. After adjustment, T-score was inversely associated with LAVI (β = - 0.358, P = 0.043) and RWT (β = - 0.003, P = 0.013). Subgroup analyses showed stronger effects in women (LAVI β = - 0.737, P = 0.001) and participants < 50 years (LAVI β = - 0.909, P = 0.022). No significant associations were observed for left ventricular mass index, ejection fraction, or diastolic function metrics. Lower BMD, measured by tibial ultrasound, is independently associated with left atrial enlargement and increased ventricular wall thickness, particularly in women and younger adults. These findings suggest shared pathophysiological mechanisms between bone loss and cardiac remodeling, warranting more in-depth research.
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