Glucocorticoid-Induced Osteoporosis

José Renan Vieira da Costa Júnior, Sérgio Luchini Batista
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Abstract

The use of glucocorticoids (GC) in the medium and long term, causes several considerable side effects, being one of the main ones the reduction of bone mineral density (BMD). Prolonged corticosteroid therapy reduces BMD by up to 20% in trabecular bone and approximately 2–3% in cortical bone in the first year of use. This loss rate declines and stabilizes at approximately 2% in subsequent years. Therefore, there is a considerable increase in the incidence of pathological fractures, whether clinically symptomatic or asymptomatic (detected as a radiological finding), which varies between 30 and 50% of patients who use GC for more than three months. In view of the above, it is essential to prevent fractures and treat osteoporosis in patients using glucocorticoids for long periods (in particular, greater than or equal to 3 months), which may or may not be associated with clinical risk factors or previous fractures. The guidelines for the treatment and prevention of this comorbidity are well established for postmenopausal women and men over 50 years of age. However, for patients below this range, studies are still lacking.
激素性骨质疏松症
中长期使用糖皮质激素(GC)会引起一些相当大的副作用,其中主要的副作用是降低骨密度(BMD)。在使用的第一年,长期皮质类固醇治疗可使小梁骨的骨密度降低20%,皮质骨的骨密度降低约2-3%。在随后的几年中,损失率下降并稳定在2%左右。因此,病理性骨折的发生率有相当大的增加,无论是临床症状还是无症状(作为影像学发现),在使用GC超过三个月的患者中,这一比例在30%至50%之间变化。综上所述,长期(特别是大于或等于3个月)使用糖皮质激素的患者预防骨折和治疗骨质疏松至关重要,这可能与临床危险因素或既往骨折有关,也可能无关。对于绝经后妇女和50岁以上的男性,治疗和预防这种合并症的指南已经很好地建立起来。然而,对于低于这个范围的患者,研究仍然缺乏。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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