Secondary Osteoporosis

被引:147
作者
Ebeling, Peter R. [1 ,2 ]
Nguyen, Hanh H. [1 ,2 ,3 ]
Aleksova, Jasna [2 ,4 ]
Vincent, Amanda J. [2 ,5 ]
Wong, Phillip [1 ,2 ,4 ]
Milat, Frances [1 ,2 ,4 ]
机构
[1] Monash Univ, Sch Clin Sci, Dept Med, Clayton, Vic 3168, Australia
[2] Monash Hlth, Dept Endocrinol, Clayton, Vic 3168, Australia
[3] Western Hlth, Dept Endocrinol & Diabet, Footscray, Vic 3011, Australia
[4] Hudson Inst Med Res, Clayton, Vic 3168, Australia
[5] Monash Univ, Monash Ctr Hlth Res & Implementat, Sch Publ Hlth & Preventat Med, Clayton, Vic 3168, Australia
基金
英国医学研究理事会;
关键词
osteoporosis; chronic disease; fracture; secondary causes; bone mineral density; BONE-MINERAL DENSITY; MULTIPLE-SCLEROSIS; CEREBRAL-PALSY; YOUNG-WOMEN; POSTMENOPAUSAL WOMEN; SKELETAL DEVELOPMENT; VERTEBRAL FRACTURES; HIGH PREVALENCE; INCREASED RISK; HIP FRACTURE;
D O I
10.1210/endrev/bnab028
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Osteoporosis is a global public health problem, with fractures contributing to significant morbidity and mortality. Although postmenopausal osteoporosis is most common, up to 30% of postmenopausal women, > 50% of premenopausal women, and between 50% and 80% of men have secondary osteoporosis. Exclusion of secondary causes is important, as treatment of such patients often commences by treating the underlying condition. These are varied but often neglected, ranging from endocrine to chronic inflammatory and genetic conditions. General screening is recommended for all patients with osteoporosis, with advanced investigations reserved for premenopausal women and men aged < 50 years, for older patients in whom classical risk factors for osteoporosis are absent, and for all patients with the lowest bone mass (Z-score <= -2). The response of secondary osteoporosis to conventional anti-osteoporosis therapy may be inadequate if the underlying condition is unrecognized and untreated. Bone densitometry, using dual-energy x-ray absorptiometry, may underestimate fracture risk in some chronic diseases, including glucocorticoid-induced osteoporosis, type 2 diabetes, and obesity, and may overestimate fracture risk in others (eg, Turner syndrome). FRAX and trabecular bone score may provide additional information regarding fracture risk in secondary osteoporosis, but their use is limited to adults aged >= 40 years and >= 50 years, respectively. In addition, FRAX requires adjustment in some chronic conditions, such as glucocorticoid use, type 2 diabetes, and HIV. In most conditions, evidence for antiresorptive or anabolic therapy is limited to increases in bone mass. Current osteoporosis management guidelines also neglect secondary osteoporosis and these existing evidence gaps are discussed.
引用
收藏
页码:240 / 313
页数:74
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