Tanaka Sakae, Yamamoto Takanori, Oda Eisei, Nakamura Masaki, Fujiwara Saeko
Department of Orthopaedic Surgery, Graduate School of Medicine, University of Tokyo, Hongo 7-3-1, Bunkyo-ku, Tokyo, 113-8655, Japan.
Medical Science, Lilly Research Laboratories, Medical Development Unit Japan, Eli Lilly Japan K.K., Isogami-dori, Chuo-ku, Kobe, 651-0086, Japan.
J Bone Miner Metab. 2018 Jan;36(1):87-94. doi: 10.1007/s00774-016-0809-0. Epub 2016 Dec 27.
We conducted a retrospective cohort study using a de-identified hospital administrative claims database to assess the risk of non-vertebral fracture in Japanese women with osteoporosis treated with raloxifene compared with alendronate. The study included Japanese women ≥50 years of age with newly initiated alendronate or raloxifene treatment between July 2008 and March 2013 (index date was defined as the day of first prescription for alendronate or raloxifene), and had any claim with an osteoporosis definition during the study period. A total of 37,056 patients in the database initiated treatment, and there were 4802 and 1250 patients included in the alendronate and raloxifene analysis groups, respectively. The mean observation period in the alendronate group (529.2 days) was significantly longer than that for the raloxifene group (473.5 days, P < 0.001). Non-vertebral fractures accumulated linearly, at a similar rate, for both study drugs: incidence at 1 year was 2.83 and 2.64% for the alendronate and raloxifene groups, respectively. For the relative risk of non-vertebral fracture within 1 year, the adjusted hazard ratio was 0.933 for raloxifene versus alendronate, indicating that the relative risk of non-vertebral fracture was similar for the two drugs. The effectiveness of raloxifene in preventing non-vertebral fractures in Japanese women with osteoporosis was similar to that of alendronate. Therefore, raloxifene may be worthy of consideration as an alternative treatment.
我们进行了一项回顾性队列研究,使用去识别化的医院管理索赔数据库,以评估与阿仑膦酸钠相比,接受雷洛昔芬治疗的日本骨质疏松症女性发生非椎体骨折的风险。该研究纳入了2008年7月至2013年3月期间开始新使用阿仑膦酸钠或雷洛昔芬治疗的年龄≥50岁的日本女性(索引日期定义为首次开具阿仑膦酸钠或雷洛昔芬处方的日期),且在研究期间有任何符合骨质疏松症定义的索赔记录。数据库中共有37056名患者开始治疗,阿仑膦酸钠分析组和雷洛昔芬分析组分别有4802名和1250名患者。阿仑膦酸钠组的平均观察期(529.2天)显著长于雷洛昔芬组(473.5天,P<0.001)。两种研究药物的非椎体骨折均呈线性累积,累积速率相似:阿仑膦酸钠组和雷洛昔芬组1年时的发病率分别为2.83%和2.64%。对于1年内非椎体骨折的相对风险,雷洛昔芬与阿仑膦酸钠相比的调整后风险比为0.933,表明两种药物的非椎体骨折相对风险相似。雷洛昔芬在预防日本骨质疏松症女性非椎体骨折方面的有效性与阿仑膦酸钠相似。因此,雷洛昔芬可能值得作为一种替代治疗方法加以考虑。