New simulation model for bone formation markers in osteoporosis patients treated with once-weekly teriparatide

被引:0
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作者
Sakae Tanaka [1 ]
Taiji Adachi [2 ]
Tatsuhiko Kuroda [3 ]
Toshitaka Nakamura [4 ]
Masataka Shiraki [5 ]
Toshitsugu Sugimoto [6 ]
Yasuhiro Takeuchi [7 ]
Mitsuru Saito [8 ]
John P Bilezikian [9 ]
机构
[1] Department of Orthopaedic Surgery,Faculty of Medicine,University of Tokyo,Tokyo,Japan
[2] Department of Biomechanics,Institute for Frontier Medical Sciences,Kyoto University,Kyoto,Japan
[3] Medical Affairs Department,Asahi Kasei Pharma Corporation,Tokyo,Japan
[4] National Center for Global Health and Medicine,Tokyo,Japan
[5] Research Institute and Practice for Involutional Diseases,Nagano,Japan
[6] Internal Medicine ,Shimane University Faculty of Medicine,Izumo,Japan
[7] Toranomon Hospital Endocrine Center,Tokyo,Japan
[8] Department of Orthopaedic Surgery,Jikei University School of Medicine,Tokyo,Japan
[9] Metabolic Bone Diseases Program,Division of Endocrinology,Department of Medicine,College of Physicians and Surgeons,Columbia University,New
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摘要
Daily 20-mg and once-weekly 56.5-mg teriparatide(parathyroid hormone 1–34) treatment regimens increase bone mineral density(BMD) and prevent fractures, but changes in bone turnover markers differ between the two regimens. The aim of the present study was to explain changes in bone turnover markers using once-weekly teriparatide with a simulation model. Temporary increases in bone formation markers and subsequent decreases were observed during once-weekly teriparatide treatment for 72 weeks. These observations support the hypothesis that repeated weekly teriparatide administration stimulates bone remodeling, replacing old bone with new bone and leading to a reduction in the active remodeling surface. A simulation model was developed based on the iterative remodeling cycle that occurs on residual old bone. An increase in bone formation and a subsequent decrease were observed in the preliminary simulation. For each fitted time point, the predicted value was compared to the absolute values of the bone formation and resorption markers and lumbar BMD. The simulation model strongly matched actual changes in bone turnover markers and BMD. This simulation model indicates increased bone formation marker levels in the early stage and a subsequent decrease. It is therefore concluded that remodeling-based bone formation persisted during the entire treatment period with once-weekly teriparatide.
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