Watts Nelson B
University of Cincinnati College of Medicine, University of Cincinnati Bone Health and Osteoporosis Center, Cincinnati, OH, USA.
Clin Geriatr Med. 2003 May;19(2):395-414. doi: 10.1016/s0749-0690(02)00069-1.
Bisphosphonates represent the agents of choice for most patients with osteoporosis. They are the best studied of all agents for the prevention of bone loss and reduction in fractures. They increase BMD, primarily at the lumbar spine, but also at the proximal femur. In patients who have established osteoporosis, bisphosphonates reduce the risk of vertebral fractures, and are the only agents in prospective trials to reduce the risk of hip fractures and other nonvertebral fractures. Bisphosphonates reduce the risk of fracture quickly. The risk of radiographic vertebral deformities is reduced after 1 year of treatment with risedronate [68]. The risk of clinical vertebral fractures is reduced after 1 year of treatment with alendronate [69] and just 6 months' treatment with risedronate [157]. The antifracture effect of risedronate has been shown to continue through 5 years of treatment [158]. Alendronate and risedronate are approved by the FDA for prevention of bone loss in recently menopausal women, for treatment of postmenopausal osteoporosis, and for prevention (risedronate) and treatment (alendronate and risedronate) of glucocorticoid-induced osteoporosis. Alendronate is also approved for treatment of osteoporosis in men. Other bisphosphonates (etidronate for oral use, pamidronate and zoledronate for intravenous infusion) are also available and can be used off label for patients who cannot tolerate approved agents. Although bisphosphonates combined with estrogen or raloxifene produce greater gains in bone mass compared with single-agent treatment, the use of two antiresorptive agents in combination cannot be recommended because the benefit on fracture risk has not been demonstrated and because of increased cost and side effects.
双膦酸盐是大多数骨质疏松症患者的首选药物。它们是所有预防骨质流失和减少骨折药物中研究最充分的。它们主要增加腰椎的骨密度,但也能增加股骨近端的骨密度。在已确诊骨质疏松症的患者中,双膦酸盐可降低椎体骨折的风险,并且是前瞻性试验中唯一能降低髋部骨折和其他非椎体骨折风险的药物。双膦酸盐能迅速降低骨折风险。使用利塞膦酸钠治疗1年后,影像学椎体畸形的风险降低[68]。使用阿仑膦酸钠治疗1年后以及使用利塞膦酸钠仅治疗6个月后,临床椎体骨折的风险降低[69,157]。利塞膦酸钠的抗骨折作用已被证明可持续至治疗5年[158]。阿仑膦酸钠和利塞膦酸钠已获美国食品药品监督管理局(FDA)批准,用于预防近期绝经后女性的骨质流失、治疗绝经后骨质疏松症以及预防(利塞膦酸钠)和治疗(阿仑膦酸钠和利塞膦酸钠)糖皮质激素诱导的骨质疏松症。阿仑膦酸钠还被批准用于治疗男性骨质疏松症。其他双膦酸盐(口服依替膦酸二钠、静脉输注帕米膦酸二钠和唑来膦酸)也可供使用,对于无法耐受已获批药物的患者可用于非适应证用药。尽管与单药治疗相比,双膦酸盐与雌激素或雷洛昔芬联合使用能使骨量增加更多,但不推荐联合使用两种抗吸收药物,因为尚未证明其对骨折风险有益,且成本增加和副作用增多。