Vestergaard Peter
The Osteoporosis Clinic Aarhus Amtssygehus, Aarhus University Hospital, Aarhus, Denmark.
Treat Endocrinol. 2005;4(5):263-77. doi: 10.2165/00024677-200504050-00001.
Osteoporosis is a condition associated with decreased bone strength and an increased fracture risk. It may be defined based on bone mineral density (BMD) with a T-score at the hip or spine of less than -2.5 standard deviations in young healthy individuals or from an osteoporotic fracture (i.e. a fracture occurring after low-energy trauma or no apparent trauma). Risk factors predisposing to fractures include: increasing age; female gender; low BMD; a prior fragility fracture; a family history of fragility fractures; low bodyweight; lack of estrogen in women (i.e. post menopause); corticosteroid use; smoking; a number of diseases; deficiency in calcium and vitamin D; an increased risk of falls (i.e. impaired vision); immobilization; and Caucasian race. The more risk factors that are present the higher the risk of fractures over the following 10 years. The need to initiate preventive therapy with anti-osteoporotic treatment increases steeply with the absolute fracture risk. Indications for referral for dual energy x-ray absorptiometry measurement of BMD include: age >65 years; age <65 years in postmenopausal women with any of the risk factors already mentioned; premature menopause (<45 years); prolonged amenorrhea (>1 year) in younger women; fragility fractures; and diseases or conditions known to lead to osteoporosis.Anti-resorptive therapies include calcium plus vitamin D, bisphosphonates (alendronate, etidronate, risedronate, ibandronate), selective estrogen receptor modulators (raloxifene), hormone replacement therapy, and calcitonin. Guidelines from several countries on when to initiate anti-resorptive therapy state that therapy may be started in patients with a prior fragility fracture (some guidelines state that in this situation no BMD measurements are necessary) or in patients with a T-score of less than -2.5 (some guidelines state that additional risk factors need to be present in this situation). Some guidelines state that anti-resorptive therapy may be initiated in patients with a T-score in the osteopenic range (from -1 to -2.5, i.e. not frank osteoporosis) in the presence of other risk factors. The cost effectiveness of anti-resorptive therapy increases with the absolute fracture risk. In some scenarios, treatment with bisphosphonates may be cost effective in a 50-year-old woman with an absolute hip fracture risk of >or=1.1% over the next 10 years.
骨质疏松症是一种与骨强度降低和骨折风险增加相关的病症。它可以根据骨矿物质密度(BMD)来定义,在年轻健康个体中,髋部或脊柱的T值小于 -2.5个标准差,或者根据骨质疏松性骨折(即低能量创伤后或无明显创伤后发生的骨折)来定义。导致骨折的危险因素包括:年龄增长;女性性别;低骨密度;既往脆性骨折;脆性骨折家族史;低体重;女性体内雌激素缺乏(即绝经后);使用皮质类固醇;吸烟;多种疾病;钙和维生素D缺乏;跌倒风险增加(即视力受损);固定不动;以及白种人。存在的危险因素越多,未来10年内发生骨折的风险就越高。随着绝对骨折风险的增加,启动抗骨质疏松治疗进行预防的必要性也急剧增加。推荐进行双能X线吸收法测量骨密度的指征包括:年龄>65岁;有上述任何危险因素的绝经后女性年龄<65岁;过早绝经(<45岁);年轻女性长期闭经(>1年);脆性骨折;以及已知会导致骨质疏松症的疾病或状况。抗吸收治疗包括钙加维生素D、双膦酸盐(阿仑膦酸钠、依替膦酸二钠、利塞膦酸钠、伊班膦酸钠)、选择性雌激素受体调节剂(雷洛昔芬)、激素替代疗法和降钙素。几个国家关于何时开始抗吸收治疗的指南指出,对于既往有脆性骨折的患者(一些指南指出在这种情况下无需进行骨密度测量)或T值小于 -2.5的患者(一些指南指出在这种情况下还需要存在其他危险因素)可以开始治疗。一些指南指出,在存在其他危险因素的情况下,对于骨量减少范围(-1至 -2.5,即非明显骨质疏松症)T值的患者可以启动抗吸收治疗。抗吸收治疗的成本效益随着绝对骨折风险的增加而提高。在某些情况下,对于一名50岁女性,未来10年内绝对髋部骨折风险≥1.1%,使用双膦酸盐治疗可能具有成本效益。