Abstract

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.

Keywords

TeriparatideDenosumabMedicineOsteoporosisIntensive care medicineBone healthBone mineralPediatricsInternal medicine

MeSH Terms

AgedBone DensityBone Density Conservation AgentsDenosumabDiphosphonatesFemaleHumansMaleMiddle AgedOsteoporosisOsteoporotic FracturesParathyroid Hormone-Related ProteinRisk FactorsTeriparatide

Affiliated Institutions

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Publication Info

Year
2019
Type
review
Volume
393
Issue
10169
Pages
364-376
Citations
2038
Access
Closed

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2038
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Cite This

Juliet Compston, Michael R. McClung, William D. Leslie (2019). Osteoporosis. The Lancet , 393 (10169) , 364-376. https://doi.org/10.1016/s0140-6736(18)32112-3

Identifiers

DOI
10.1016/s0140-6736(18)32112-3
PMID
30696576

Data Quality

Data completeness: 81%