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   <subfield code="a">Efficacy and safety of odanacatib treatment for patients with osteoporosis: a meta-analysis</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Shi Feng, Zhicheng Luo, Da Liu]</subfield>
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   <subfield code="a">The aim of this study was to evaluate the efficacy and safety of odanacatib (ODN) for the treatment of osteoporosis, using data in studies reported in the literature. We performed a literature search to compare the outcomes of applications of once-weekly ODN 50mg and control. The outcomes of osteoporosis evaluated include primary outcome as bone mineral density (BMD) at different skeletal sites, and secondary outcomes, including adverse events (AEs), such as incidence of skin AEs, fracture, and serious adverse events (SAEs). Four trials were included. Mean difference (95% CI) of lumbar spine BMD was 3.41 (1.57-5.24) at 12months and 4.89 (2.72-7.05) at 24months; mean difference (95% CI) of femoral neck BMD was 1.90 (0.73-3.08) at 12months and 3.85 (2.55-5.15) at 24months; mean difference (95% CI) of total hip BMD was 2.65 (1.20-4.09) at 12months and 3.70 (1.76-5.64) at 24months; risk ratio (95% CI) of AEs was 0.98 (0.91-1.07); risk ratio (95% CI) of SAEs was 1.11 (0.72-1.72); risk ratio (95% CI) of skin AEs was 0.92 (0.63-1.35); and risk ratio (95% CI) of fracture was 0.34 (0.16-0.70). In this study, application of 50mg ODN produced significantly greater BMD increases and lower fracture incidence than that of the control. In addition, ODN was generally well tolerated.</subfield>
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   <subfield code="a">The Japanese Society for Bone and Mineral Research and Springer Japan, 2014</subfield>
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   <subfield code="a">Odanacatib</subfield>
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   <subfield code="u">Department of Orthopaedic Surgery, Shengjing Hospital, China Medical University, 36 Sanhao Road, 110004, Shenyang, China</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
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