Glucocorticoid-induced osteoporosis: From basic mechanisms to clinical aspects

被引:32
作者
Alesci, S
De Martino, MU
Ilias, I
Gold, PW
Chrousos, GP
机构
[1] NIMH, Clin Neuroendocrinol Branch, NIH, Bethesda, MD 20892 USA
[2] NICHHD, Pediat & Reprod Endocrinol Branch, NIH, Bethesda, MD 20892 USA
[3] Univ Patras, Fac Med, Dept Pharmacol, Patras, Greece
关键词
glucocorticoids; bone; osteoporosis; fracture;
D O I
10.1159/000082360
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Glucocorticoid (GC)-induced osteoporosis (GCOP) is the most common cause of osteoporosis in adults aged 20 45 years as well as the most common cause of iatrogenic osteoporosis. GC excess, either endogenous or exogenous, induces bone loss in 30 - 50% of cases. Indeed, bone loss leading to fractures is perhaps the most incapacitating, sometimes partially irreversible, complication of GC therapy. Nevertheless, GCOP is often underdiagnosed and left untreated. The following article provides an update on the cellular and molecular mechanisms implicated in the pathophysiology of GC- induced bone loss, as well as some guidelines on diagnostic, preventive and therapeutic strategies for this medical condition, in an effort to promote a better knowledge and greater awareness of GCOP by both the patient and the physician. Copyright (C) 2005 S. Karger AG, Basel.
引用
收藏
页码:1 / 19
页数:19
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