Laboratory of Osteoblast Biology and Pathology, INSERM, U606, Paris 75475, France.
Osteoporos Int. 2011 Jun;22(6):1659-67. doi: 10.1007/s00198-010-1369-0. Epub 2010 Sep 2.
Oestrogen deficiency increases the rate of bone remodelling which, in association with a negative remodelling balance (resorption exceeding formation), results in impaired bone architecture, mass and strength. Current anti-osteoporotic drugs act on bone remodelling by inhibiting bone resorption or by promoting its formation. An alternative therapeutic approach is based on the concept of inducing opposite effects on bone resorption and formation. One therapeutic agent, strontium ranelate, was shown to induce opposite effects on bone resorption and formation in pre-clinical studies and to reduce fracture risk in postmenopausal osteoporotic patients. How strontium ranelate acts to improve bone strength in humans remains a matter of debate, however. This review of the most recent pre-clinical and clinical studies is a critical analysis of strontium ranelate's action on bone resorption and formation and how it increases bone mass, microarchitecture and strength in postmenopausal osteoporotic women.
雌激素缺乏会增加骨重塑的速度,这与负性重塑平衡(吸收超过形成)相关,导致骨结构、质量和强度受损。目前的抗骨质疏松药物通过抑制骨吸收或促进其形成来作用于骨重塑。一种替代的治疗方法基于诱导骨吸收和形成相反作用的概念。一种治疗剂,雷奈酸锶,在临床前研究中显示出对骨吸收和形成的相反作用,并降低绝经后骨质疏松症患者的骨折风险。然而,雷奈酸锶如何在人体中增强骨强度仍然存在争议。这篇对最新的临床前和临床研究的综述是对雷奈酸锶对骨吸收和形成作用的批判性分析,以及它如何增加绝经后骨质疏松妇女的骨量、微结构和强度。