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Bone status in men with heart failure: results from the Studies Investigating Co-morbidities Aggravating Heart
Goran Loncar1,2,3, Tania Garfias-Veitl3,4, Miroslava Valentova3,4
1Dedinje Cardiovascular Institute, Belgrade, Serbia.
Insights
Men with heart failure (HF) experience bone loss over time. Lower bone mineral density (BMD) in HF patients is linked to poorer survival, with osteocalcin and osteoprotegerin as key indicators.
Area of Science:
- Cardiology
- Endocrinology
- Geriatrics
Background:
- Heart failure (HF) is associated with various comorbidities, including metabolic disturbances.
- Bone metabolism alterations are increasingly recognized in patients with chronic diseases like HF.
- Assessing bone status in men with HF is crucial for understanding disease progression and patient outcomes.
Purpose of the Study:
- To evaluate bone mineral density (BMD) at the hip in men diagnosed with heart failure (HF).
- To identify potential correlations between BMD, bone turnover markers, and clinical parameters in HF patients.
- To determine the prognostic value of BMD and bone markers for survival in this population.
Main Methods:
- Dual-energy X-ray absorptiometry (DXA) was used to measure hip bone mineral density (BMD) in 141 male patients with HF.
- Markers of bone metabolism, including osteocalcin and osteoprotegerin, were analyzed.
- Patient survival was tracked over an 8-year follow-up period, with statistical analyses performed to identify predictors of outcomes.
Main Results:
- Patients with lower hip BMD were older, more likely to be sarcopenic, and had lower peak oxygen consumption compared to those with higher BMD.
- Elevated levels of osteoprotegerin and osteocalcin were observed in patients with lower BMD.
- A significant reduction in BMD was noted over a 30-month follow-up period in a subset of patients.
- Serum osteocalcin independently predicted lower hip BMD, while hip BMD and serum osteoprotegerin independently predicted impaired survival.
Conclusions:
- Heart failure patients experience progressive bone mineral density (BMD) loss.
- Osteocalcin serves as an independent marker for lower hip BMD, and osteoprotegerin predicts mortality in HF patients.
- Early assessment of BMD and bone turnover markers in HF patients may allow for timely interventions to improve prognosis.
Aim:
To assess bone status expressed as hip bone mineral density (BMD) in men with heart failure (HF).
Methods And Results:
A total of 141 male patients with HF underwent dual energy X-ray absorptiometry to assess their BMD. We analysed markers of bone metabolism. Patients were classified as lower versus higher BMD according to the median hip BMD (median = 1.162 g/cm2 ). Survival was assessed over 8 years of follow-up. Patients with lower BMD were older (71 ± 10 vs. 66 ± 9 years, p = 0.004), more likely to be sarcopenic (37% vs. 7%, p < 0.001) and to have lower peak oxygen consumption (absolute peak VO2 1373 ± 480 vs. 1676 ± 447 ml/min, p < 0.001), had higher osteoprotegerin and osteocalcin levels (both p < 0.05) compared to patients with higher BMD. Among 47 patients with repeated BMD assessments, a significant reduction in BMD was noted over 30 months of follow-up. In multivariate logistic regression analysis, serum osteocalcin remained independently related with lower BMD (odds ratio [OR] 1.738, 95% confidence interval [CI] 1.136-2.660, p = 0.011). Hip BMD and serum osteoprotegerin were independent predictors of impaired survival on Cox proportional hazard analysis (hazard ratio [HR] 0.069, 95% CI 0.011-0.444, p = 0.005, and HR 0.638, 95% CI 0.472-0.864, p = 0.004, respectively).
Conclusions:
Patients with HF lose BMD over time. Markers of bone turnover can help in identifying patients at risk with osteocalcin being an independent marker of lower hip BMD and osteoprotegerin an independent predictor of death. HF patients with increased osteocalcin and osteoprotegerin may benefit from BMD assessment as manifest osteoporosis seems to be too late for clinically meaningful intervention in HF.
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