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Randomized Teriparatide [Human Parathyroid Hormone (PTH) 1–34] Once-Weekly Efficacy Research (TOWER) Trial for Examining the Reduction in New Vertebral Fractures in Subjects with Primary Osteoporosis and High Fracture Risk

特立帕肽 医学 骨质疏松症 安慰剂 股骨颈 骨矿物 相对风险 随机对照试验 骨密度 入射(几何) 外科 临床终点 置信区间 内科学 泌尿科 物理 替代医学 病理 光学
作者
Toshitaka Nakamura,Toshitsugu Sugimoto,Tetsuo Nakano,Hideaki Kishimoto,Masako Ito,Masao Fukunaga,Hiroshi Hagino,Teruki Sone,Hideki Yoshikawa,Yoshiki Nishizawà,Takuo Fujita,Masataka Shiraki
出处
期刊:The Journal of Clinical Endocrinology and Metabolism [The Endocrine Society]
卷期号:97 (9): 3097-3106 被引量:250
标识
DOI:10.1210/jc.2011-3479
摘要

Weekly teriparatide injection at a dose of 56.5 μg has been shown to increase bone mineral density.A phase 3 study was conducted to determine the efficacy of once-weekly teriparatide injection for reducing the incidence of vertebral fractures in patients with osteoporosis.In this randomized, multicenter, double-blind, placebo-controlled trial conducted in Japan, the incidence of morphological vertebral fractures by radiographs was assessed.Subjects were 578 Japanese patients between the ages of 65 and 95 yr who had prevalent vertebral fracture.Subjects were randomly assigned to receive once-weekly s.c. injections of teriparatide (56.5 μg) or placebo for 72 wk.The primary endpoint was the incidence of new vertebral fracture.Once-weekly injections of teriparatide reduced the risk of new vertebral fracture with a cumulative incidence of 3.1% in the teriparatide group, compared with 14.5% in the placebo group (P < 0.01), and a relative risk of 0.20 (95% confidence interval, 0.09 to 0.45). At 72 wk, teriparatide administration increased bone mineral density by 6.4, 3.0, and 2.3% at the lumbar spine, the total hip, and the femoral neck, respectively, compared with the placebo (P < 0.01). Adverse events (AE) and the dropout rates by AE were more frequently experienced in the teriparatide group, but AE were generally mild and tolerable.Weekly s.c. administration of teriparatide at a dose of 56.5 μg may provide another option of anabolic treatments in patients with osteoporosis at higher fracture risk.
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