Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), 33011 Oviedo, Spain.
Redes de Investigación Cooperativa Orientadas a Resultados en Salud (RICORS), RICORS2040 (Kidney Disease), 28040 Madrid, Spain.
Nutrients. 2024 Feb 22;16(5):605. doi: 10.3390/nu16050605.
Bone represents a metabolically active tissue subject to continuous remodeling orchestrated by the dynamic interplay between osteoblasts and osteoclasts. These cellular processes are modulated by a complex interplay of biochemical and mechanical factors, which are instrumental in assessing bone remodeling. This comprehensive evaluation aids in detecting disorders arising from imbalances between bone formation and reabsorption. Osteoporosis, characterized by a reduction in bone mass and strength leading to heightened bone fragility and susceptibility to fractures, is one of the more prevalent chronic diseases. Some epidemiological studies, especially in patients with chronic kidney disease (CKD), have identified an association between osteoporosis and vascular calcification. Notably, low bone mineral density has been linked to an increased incidence of aortic calcification, with shared molecules, mechanisms, and pathways between the two processes. Certain molecules emerging from these shared pathways can serve as biomarkers for bone and mineral metabolism. Detecting and evaluating these alterations early is crucial, requiring the identification of biomarkers that are reliable for early intervention. While traditional biomarkers for bone remodeling and vascular calcification exist, they suffer from limitations such as low specificity, low sensitivity, and conflicting results across studies. In response, efforts are underway to explore new, more specific biomarkers that can detect alterations at earlier stages. The aim of this review is to comprehensively examine some of the emerging biomarkers in mineral metabolism and their correlation with bone mineral density, fracture risk, and vascular calcification as well as their potential use in clinical practice.
骨骼是一种代谢活跃的组织,不断受到成骨细胞和破骨细胞之间动态相互作用的调节。这些细胞过程受到生化和机械因素的复杂相互作用的调节,这些因素对于评估骨重塑至关重要。这种全面的评估有助于发现由于骨形成和吸收之间的不平衡而引起的疾病。骨质疏松症是一种常见的慢性疾病,其特征是骨量和骨强度减少,导致骨脆性增加,易发生骨折。一些流行病学研究,特别是在慢性肾脏病(CKD)患者中,已经确定了骨质疏松症与血管钙化之间的关联。值得注意的是,低骨密度与主动脉钙化的发生率增加有关,这两个过程之间存在共同的分子、机制和途径。这些共同途径中出现的某些分子可以作为骨和矿物质代谢的生物标志物。早期发现和评估这些变化至关重要,需要识别可靠的早期干预生物标志物。虽然存在用于骨重塑和血管钙化的传统生物标志物,但它们存在特异性低、灵敏度低以及研究之间结果不一致等局限性。因此,正在努力探索新的、更特异的生物标志物,以更早地检测到变化。本综述的目的是全面检查矿物质代谢中一些新兴的生物标志物及其与骨矿物质密度、骨折风险和血管钙化的相关性,以及它们在临床实践中的潜在用途。