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The bone-heart axis: A crucial dialogue in cardiovascular disease
Ying Liu1, Qi Yao1, Jiabin Yu1
1Department of Cardiology, Renmin Hospital of Wuhan University, Wuhan 430060, PR China; Hubei Key Laboratory of Metabolic and Chronic Diseases, Wuhan 430060, PR China.
Insights
The skeletal system influences cardiovascular diseases (CVDs) through the "bone-heart axis". Understanding this crosstalk is key for developing new treatments for conditions like atherosclerosis and heart failure.
Area of Science:
- Endocrinology
- Cardiovascular Medicine
- Skeletal Biology
Background:
- Cardiovascular diseases (CVDs) are a leading cause of death globally.
- The skeletal system plays an endocrine role, influencing cardiovascular health.
- Emerging research highlights the
- bone-heart axis
- a bidirectional communication network between bone and heart.
Purpose of the Study:
- To explore the role of osteocrine factors in cardiovascular regulation.
- To elucidate the mechanisms of the bone-heart axis in CVD pathogenesis.
- To advocate for a shift towards understanding interorgan communication for therapeutic development.
Main Methods:
- Review of current scientific literature on osteocrine factors and CVDs.
- Analysis of the regulatory networks between skeletal and cardiovascular systems.
- Investigation of pathological processes influenced by the bone-heart axis.
Main Results:
- Osteocrine factors (FGF23, LCN2, DKK1, MYDGF, OCN, SOST) are implicated in cardiovascular regulation.
- The bone-heart axis influences mineral metabolism, vascular calcification, and myocardial energy.
- Dysregulation of this axis accelerates atherosclerosis (AS) and heart failure (HF).
Conclusions:
- The bone-heart axis is a critical determinant of cardiovascular health.
- Understanding the spatiotemporal dynamics of this axis is essential for precision medicine.
- Targeting the bone-heart crosstalk offers potential for integrated skeletal and cardiovascular protection.
Abstract:
Cardiovascular diseases (CVDs), the leading cause of global mortality, are now understood to be profoundly influenced by the endocrine regulatory functions of the skeletal system. Emerging evidence suggests that osteocrine factors, including fibroblast growth factor-23 (FGF23), lipocalin-2 (LCN2), Dickkopf-1 (DKK1), myeloid-derived growth factor (MYDGF), osteocalcin (OCN), and sclerostin (SOST), establish bidirectional regulatory networks with the cardiovascular system, termed the "bone-heart axis". This axis regulates critical pathological processes, including mineral metabolism, vascular calcification, and myocardial energy homeostasis. Dysregulation of this crosstalk accelerates the progression of atherosclerosis (AS), heart failure (HF), and other CVDs. Therefore, current research necessitates a paradigm shift from univariate analyses to elucidating the spatiotemporal dynamics of interorgan communication, thereby facilitating the development of precision therapeutic strategies for integrated skeletal and cardiovascular protection.
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