Drug-induced Osteoporosis: Mechanisms and Clinical Implications

被引:190
作者
Mazziotti, Gherardo
Canalis, Ernesto [2 ,3 ]
Giustina, Andrea [1 ]
机构
[1] Univ Brescia, Dept Med & Surg Sci, Serv Endocrinol, I-25018 Montichiari, Italy
[2] St Francis Hosp & Med Ctr, Dept Res, Hartford, CT 06105 USA
[3] Univ Connecticut, Sch Med, Farmington, CT USA
关键词
Drugs; Fractures; Osteoporosis; Secondary osteoporosis; ANDROGEN-DEPRIVATION THERAPY; BONE-MINERAL DENSITY; GLUCOCORTICOID-INDUCED OSTEOPOROSIS; THYROID-STIMULATING HORMONE; RANDOMIZED CONTROLLED-TRIAL; PROSTATE-CANCER; POSTMENOPAUSAL WOMEN; BREAST-CANCER; FRACTURE RISK; MEDROXYPROGESTERONE ACETATE;
D O I
10.1016/j.amjmed.2010.02.028
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Drug-induced osteoporosis is common and has a significant impact on the prognosis of patients suffering from chronic debilitating diseases. Glucocorticoids are the drugs causing osteoporotic fractures most frequently, but osteoporosis with fractures is observed also in women treated with aromatase inhibitors for breast cancer, in men receiving anti-androgen therapy for prostate cancer, in postmenopausal women treated with high doses of thyroxine, and in men and women treated with thiazolinediones for type 2 diabetes mellitus. Bone loss with fractures also occurs in patients treated with drugs targeting the immune system, such as calcineurin inhibitors, antiretroviral drugs, selective inhibitors of serotonin reuptake, anticonvulsants, loop diuretics, heparin, oral anticoagulants, and proton pump inhibitors. (C) 2010 Elsevier Inc. All rights reserved. The American Journal of Medicine (2010) 123, 877-884
引用
收藏
页码:877 / 884
页数:8
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