Department of Medicine, Cambridge Biomedical Campus, Cambridge, UK.
Department of Medicine, Oregon Health and Science University, Portland, OR, USA; Mary MacKillop Institute for Health, Australian Catholic University, Melbourne, VIC, Australia.
Lancet. 2019 Jan 26;393(10169):364-376. doi: 10.1016/S0140-6736(18)32112-3.
Fractures resulting from osteoporosis become increasingly common in women after age 55 years and men after age 65 years, resulting in substantial bone-associated morbidities, and increased mortality and health-care costs. Research advances have led to a more accurate assessment of fracture risk and have increased the range of therapeutic options available to prevent fractures. Fracture risk algorithms that combine clinical risk factors and bone mineral density are now widely used in clinical practice to target high-risk individuals for treatment. The discovery of key pathways regulating bone resorption and formation has identified new approaches to treatment with distinctive mechanisms of action. Osteoporosis is a chronic condition and long-term, sometimes lifelong, management is required. In individuals at high risk of fracture, the benefit versus risk profile is likely to be favourable for up to 10 years of treatment with bisphosphonates or denosumab. In people at a very high or imminent risk of fracture, therapy with teriparatide or abaloparatide should be considered; however, since treatment duration with these drugs is restricted to 18-24 months, treatment should be continued with an antiresorptive drug. Individuals at high risk of fractures do not receive adequate treatment and strategies to address this treatment gap-eg, widespread implementation of Fracture Liaison Services and improvement of adherence to therapy-are important challenges for the future.
骨质疏松症导致的骨折在女性中 55 岁以后、男性中 65 岁以后变得越来越常见,导致大量与骨骼相关的发病率和死亡率增加,以及医疗保健费用增加。研究进展使得对骨折风险的评估更加准确,并增加了预防骨折的治疗选择范围。目前,将临床危险因素和骨密度相结合的骨折风险算法已广泛用于临床实践,以针对高风险人群进行治疗。调节骨吸收和形成的关键途径的发现为具有独特作用机制的治疗方法开辟了新途径。骨质疏松症是一种慢性疾病,需要长期甚至终身管理。在骨折风险高的个体中,使用双膦酸盐或地舒单抗治疗 10 年的获益与风险比可能是有利的。对于骨折风险非常高或即将发生骨折的患者,应考虑使用特立帕肽或abaloparatide 治疗;然而,由于这些药物的治疗持续时间限于 18-24 个月,因此应继续使用抗吸收药物进行治疗。骨折风险高的个体并未接受充分的治疗,解决这一治疗差距的策略(例如,广泛实施骨折联络服务和提高治疗依从性)是未来的重要挑战。