Study finds risk factors for vertebral fractures and bone loss after denosumab discontinuation
Denosumab reduces bone resorption and improves bone mineral density (BMD). A recent study suggests that the age, treatment duration, and prior bisphosphonate therapy are all associated with potential bone mineral density (BMD) loss following the discontinuation of denosumab therapy. The study findings were published in the journal Bone on December 26, 2020.
Unlike bisphosphonates, denosumab is not incorporated into the bone. Therefore, its effect on bone resorption stops after treatment discontinuation. Denosumab discontinuation without subsequent bisphosphonates (BPs) is associated with bone loss and multiple vertebral fractures. However, the risk factors of bone loss and multiple fractures remain unclear. Therefore, researchers of Switzerland conducted a study to identify the risk factors for bone loss and vertebral fractures after denosumab discontinuation.
It was a retrospective study of 219 women with osteoporosis who discontinued denosumab treatment and received subsequent treatment with zoledronate, other BPs or a selective estrogen receptor modulator (SERM), or no therapy. Researchers analyzed the fracture rate, longitudinal bone mineral density (BMD) changes and bone turnover markers (BTMs) within 2years after denosumab discontinuation. They used the linear regression model, to evaluate the loss of BMD and age, BMI (kg/m2), denosumab treatment duration, pre-treatment, prior fracture state, baseline T-scores, use of glucocorticoids or aromatase inhibitors and BMD gains under denosumab therapy.
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