Bone status in men with heart failure: results from the Studies Investigating Co‐morbidities Aggravating Heart Failure

Author:

Loncar Goran123,Garfias‐Veitl Tania34,Valentova Miroslava34,Vatic Mirela34,Lainscak Mitja5,Obradović Danilo6,Dschietzig Thomas Bernd7,Doehner Wolfram8910,Jankowska Ewa A.1112,Anker Stefan D.81013,von Haehling Stephan34

Affiliation:

1. Dedinje Cardiovascular Institute Belgrade Serbia

2. Faculty of Medicine University of Belgrade Belgrade Serbia

3. Department of Cardiology and Pneumology University Medical Center Goettingen, Georg‐ August University Goettingen Germany

4. German Center for Cardiovascular Research (DZHK) Partner Site Goettingen Goettingen Germany

5. Department of Internal Medicine, General Hospital Murska Sobota and Faculty of Medicine University of Ljubljana Ljubljana Slovenia

6. Department of Cardiology/Internal Medicine Heart Center Leipzig‐University Leipzig Leipzig Germany

7. Immundiagnostik AG Neuruppin Germany

8. Berlin Institute of Health‐Center for Regenerative Therapies (BCRT) Charité‐ Universitätsmedizin Berlin Berlin Germany

9. Department of Cardiology (Virchow Klinikum) Charité University Medical Center Berlin Berlin Germany

10. German Center for Cardiovascular Research (DZHK) Partner Site Berlin Berlin Germany

11. Department of Translational Cardiology and Clinical Registries, Institute of Heart Diseases Wroclaw Medical University Wroclaw Poland

12. Institute of Heart Diseases University Hospital Wroclaw Poland

13. Division of Cardiology and Metabolism ‐ Heart Failure, Cachexia & Sarcopenia, Department of Cardiology (Virchow Klinikum) Charité University Medical Center Berlin Berlin Germany

Abstract

AimTo assess bone status expressed as hip bone mineral density (BMD) in men with heart failure (HF).Methods and resultsA 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).ConclusionsPatients 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.

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. May 2023 at a glance: focus on pathophysiology, comorbidities and devices;European Journal of Heart Failure;2023-05

2. Bones in heart failure: missing piece of the body wasting puzzle;European Journal of Heart Failure;2023-04-10

3. Chronic heart failure and osteoporosis: etiological and clinical-pathogenetic relationships;Shidnoevropejskij zurnal vnutrisnoi ta simejnoi medicini;2023

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