Iwamoto Jun, Uzawa Mitsuyoshi
Institute for Integrated Sports Medicine, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582, Japan.
Department of Orthopaedic Surgery, Keiyu Orthopaedic Hospital, Gunma, Japan.
Clin Rheumatol. 2016 Jan;35(1):205-12. doi: 10.1007/s10067-014-2812-y. Epub 2014 Nov 1.
A retrospective study was performed to evaluate the outcome of alendronate treatment for 7 years among Japanese men with osteoporosis or osteopenia and clinical risk factors for fractures. Thirty-five Japanese men with osteoporosis or osteopenia and clinical risk factors for fractures (mean age at baseline 58.2 years) who had been treated with alendronate for over 7 years in our outpatient clinic were analyzed. The lumbar spine or total hip bone mineral density (BMD) was measured using dual energy X-ray absorptiometry; the urinary levels of cross-linked N-terminal telopeptides of type I collagen (NTX) and the serum levels of alkaline phosphatase (ALP) were monitored; the incidence of fractures during the 7-year treatment period was then assessed. The urinary NTX and serum ALP levels decreased (-46.1% at 3 months and -21.1% at 7 years, respectively) and the lumbar spine and total hip BMD increased (+14.2 and +10.1% at 7 years, respectively), compared with the baseline values. Four patients (11.4%) experienced vertebral fractures, and one patient (2.9%) experienced a nonvertebral fracture. No serious adverse events were observed, including osteonecrosis of the jaw or atypical femoral fractures. These results suggested that alendronate suppressed bone turnover and increased the lumbar spine and total hip BMD from the baseline values over the course of the 7-year treatment period without causing any severe adverse events in Japanese men with osteoporosis or osteopenia and clinical risk factors for fractures.
开展了一项回顾性研究,以评估阿仑膦酸钠对患有骨质疏松症或骨量减少以及存在骨折临床风险因素的日本男性进行7年治疗的效果。分析了35名患有骨质疏松症或骨量减少以及骨折临床风险因素(基线时平均年龄58.2岁)且在我们门诊接受阿仑膦酸钠治疗超过7年的日本男性。使用双能X线吸收法测量腰椎或全髋部骨密度(BMD);监测I型胶原交联N末端肽(NTX)的尿水平和碱性磷酸酶(ALP)的血清水平;然后评估7年治疗期间的骨折发生率。与基线值相比,尿NTX和血清ALP水平下降(3个月时分别下降46.1%,7年时分别下降21.1%),腰椎和全髋部BMD增加(7年时分别增加14.2%和10.1%)。4名患者(11.4%)发生椎体骨折,1名患者(2.9%)发生非椎体骨折。未观察到严重不良事件,包括颌骨坏死或非典型股骨骨折。这些结果表明,在患有骨质疏松症或骨量减少以及骨折临床风险因素的日本男性中,阿仑膦酸钠在7年治疗期间抑制了骨转换,使腰椎和全髋部BMD较基线值增加,且未引起任何严重不良事件。