抗吸收治疗预防绝经后骨质疏松症:何时开始治疗?

Peter Vestergaard
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引用次数: 11

摘要

骨质疏松症是一种与骨强度下降和骨折风险增加有关的疾病。可根据年轻健康个体髋部或脊柱t评分小于-2.5标准差的骨密度(BMD)或骨质疏松性骨折(即低能量创伤或无明显创伤后发生的骨折)来定义。易发生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;女性缺乏雌激素(即绝经后);皮质类固醇使用;吸烟;许多疾病;缺乏钙和维生素D;摔倒的风险增加(即视力受损);固定;和高加索人种。存在的危险因素越多,在接下来的10年中发生骨折的风险就越高。预防性治疗与抗骨质疏松治疗的必要性随着绝对骨折风险的增加而急剧增加。转介双能x线骨密度测量的适应症包括:年龄>65岁;年龄1岁);脆弱性骨折;以及已知会导致骨质疏松的疾病或状况。抗再吸收治疗包括钙加维生素D、双磷酸盐(阿仑膦酸盐、地替膦酸盐、利塞膦酸盐、伊班膦酸盐)、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。一些国家关于何时开始抗再吸收治疗的指南指出,治疗可以开始于先前有脆性骨折的患者(一些指南指出在这种情况下不需要测量骨密度)或t评分低于-2.5的患者(一些指南指出在这种情况下需要存在额外的危险因素)。一些指南指出,在存在其他危险因素的情况下,t评分在骨质减少范围内(从-1到-2.5,即不是明显的骨质疏松症)的患者可以开始抗吸收治疗。抗吸收治疗的成本效益随着绝对骨折风险的增加而增加。在某些情况下,对于未来10年内髋部绝对骨折风险>或=1.1%的50岁女性,双膦酸盐治疗可能具有成本效益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-resorptive therapy for the prevention of postmenopausal osteoporosis : when should treatment begin?

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.

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