特立帕肽
德诺苏马布
骨质疏松症
医学
骨吸收
内科学
药品
骨矿物
骨形成
内分泌学
双膦酸盐
骨密度
药理学
临床试验
骨重建
重症监护医学
骨密度保护剂
药物治疗
标识
DOI:10.1210/clinem/dgaa007
摘要
The proliferation of drugs with unique modes of action for treating osteoporosis has been most welcome. Fear of complications, even though rare, associated with long-term bisphosphonates (BPs) changed prescribing patterns. The BPs are stored in bone for years. Drugs not stored in bone; for example, abaloparatide, teriparatide, denosumab, and romosozumab have expanded our armamentarium for treating osteoporosis but have brought new challenges. Bone accrued during treatment with the last 3 drugs, and perhaps abaloparatide, is lost rapidly after their withdrawal due to rebound increase in bone resorption. Treatment with these drugs must be followed by administration of an antiresorptive agent. The article by Kendler et al. (1) in this issue of JCEM reports alendronate preserves bone accrued during administration of denosumab.
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