Department of Medicine, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
Eur J Endocrinol. 2022 Sep 12;187(4):R65-R80. doi: 10.1530/EJE-22-0574. Print 2022 Oct 1.
Fractures occur in about half of older White women, and almost a third of older White men. However, 80% of the older individuals who have fractures do not meet the bone density definition of osteoporosis, suggesting that this definition is not an appropriate threshold for offering treatment. Fracture risk can be estimated based on clinical risk factors with or without bone density. A combination of calculated risk, fracture history, and bone density is used in treatment decisions. Medications available for reducing fracture risk act either to inhibit bone resorption or to promote bone formation. Romosozumab is unique in that it has both activities. Bisphosphonates are the most widely used interventions because of their efficacy, safety, and low cost. Continuous use of oral bisphosphonates for >5 years increases the risk of atypical femoral fractures, so is usually punctuated with drug holidays of 6-24 months. Denosumab is a further potent anti-resorptive agent given as 6-monthly s.c. injections. It is comparable to the bisphosphonates in efficacy and safety but has a rapid offset of effect after discontinuation so must be followed by an alternative drug, usually a bisphosphonate. Teriparatide stimulates both bone formation and resorption, substantially increases spine density, and reduces vertebral and non-vertebral fracture rates, though data for hip fractures are scant. Treatment is usually limited to 18-24 months, followed by the transition to an anti-resorptive. Romosozumab is given as monthly s.c. injections for 1 year, followed by an anti-resorptive. This sequence prevents more fractures than anti-resorptive therapy alone. Because of cost, anabolic drugs are usually reserved for those at very high fracture risk. 25-hydroxyvitamin D levels should be maintained above 30 nmol/L, using supplements if sunlight exposure is limited. Calcium intake has little effect on bone density and fracture risk but should be maintained above 500 mg/day using dietary sources.
大约一半的老年白人女性和近三分之一的老年白人男性会发生骨折。然而,80%的骨折老年人不符合骨质疏松症的骨密度定义,这表明该定义不是提供治疗的适当标准。可以根据临床危险因素,无论是否有骨密度,来评估骨折风险。计算出的风险、骨折史和骨密度结合用于治疗决策。用于降低骨折风险的药物可以通过抑制骨吸收或促进骨形成来发挥作用。罗莫索单抗的独特之处在于它具有这两种作用。双磷酸盐是最广泛使用的干预措施,因为它们具有疗效、安全性和低成本。口服双磷酸盐连续使用>5 年会增加非典型股骨骨折的风险,因此通常会用 6-24 个月的药物假期打断。地舒单抗是另一种强效的抗吸收剂,作为每 6 个月皮下注射。它在疗效和安全性方面与双磷酸盐相当,但在停药后效果迅速消退,因此必须用替代药物,通常是双磷酸盐来跟进。特立帕肽刺激骨形成和吸收,显著增加脊柱密度,并降低椎体和非椎体骨折率,但髋部骨折的数据很少。治疗通常限于 18-24 个月,然后转为抗吸收剂。罗莫索单抗每月皮下注射 1 年,然后转为抗吸收剂。这种方案比单独使用抗吸收剂可以预防更多的骨折。由于成本原因,合成代谢药物通常保留给骨折风险非常高的患者。25-羟维生素 D 水平应保持在 30 nmol/L 以上,如果阳光照射有限,则使用补充剂。钙的摄入量对骨密度和骨折风险影响不大,但应通过饮食来源维持在 500mg/天以上。