Gogakos Apostolos I, Anastasilakis Athanasios D
Department of Endocrinology, Hippokration General Hospital of Thessaloniki, Thessaloniki, Greece.
Department of Endocrinology, 424 General Military Hospital, Thessaloniki, Greece.
Expert Opin Pharmacother. 2025 Feb;26(3):265-278. doi: 10.1080/14656566.2025.2451741. Epub 2025 Jan 15.
Osteoporosis is a metabolic skeletal disease characterized by low bone mass and strength, and increased risk for fragility fractures. It is a major health issue in aging populations, due to fracture-associated increased disability and mortality. Antiresorptive treatments are first line choices in most of the cases.
Bone homeostasis is complicated, and multiple factors can compromise skeletal health. Bone turnover is a continuous process regulated by the coupled activities of bone cells that preserves skeletal strength and integrity. Imbalance between bone resorption and formation leads to bone loss and increased susceptibility to fractures. Antiresorptives prevent bone loss and reduce fracture risk, by targeting osteoclastogenesis and osteoclast function and survival. Their major drawback is the coupling of osteoclast and osteoblast activity, due to which any reduction in bone resorption is followed by suppression of bone formation.
During the last couple of decades significant progress has been made in understanding of the genetic and molecular basis of osteoporosis. Critical pathways and key molecules that mediate regulation of bone resorption have been identified. These factors may underpin novel therapeutic avenues for osteoporosis, but their potential for translation into clinical applications is yet to be tested.
骨质疏松症是一种代谢性骨骼疾病,其特征为骨量和骨强度降低,以及脆性骨折风险增加。由于骨折相关的残疾和死亡率增加,它是老年人群中的一个主要健康问题。在大多数情况下,抗吸收治疗是一线选择。
骨稳态很复杂,多种因素会损害骨骼健康。骨转换是一个由骨细胞的耦合活动调节的连续过程,可维持骨骼强度和完整性。骨吸收与骨形成之间的失衡会导致骨质流失和骨折易感性增加。抗吸收药物通过靶向破骨细胞生成、破骨细胞功能和存活来预防骨质流失并降低骨折风险。它们的主要缺点是破骨细胞与成骨细胞活动的耦合,因此任何骨吸收的减少都会随后抑制骨形成。
在过去几十年中,在理解骨质疏松症的遗传和分子基础方面取得了重大进展。已经确定了介导骨吸收调节的关键途径和关键分子。这些因素可能为骨质疏松症提供新的治疗途径,但其转化为临床应用的潜力尚待测试。