Centre for Metabolic Bone Diseases, Department of Geriatrics, University Hospitals Leuven, Leuven, Belgium.
Department of Geriatrics, Imelda Hospital, Bonheiden, Belgium.
Front Endocrinol (Lausanne). 2022 Jun 9;13:908727. doi: 10.3389/fendo.2022.908727. eCollection 2022.
Glucocorticoids are effective immunomodulatory drugs used for many inflammatory disorders as well as in transplant recipients. However, both iatrogenic and endogenous glucocorticoid excess are also associated with several side effects including an increased risk of osteoporosis and fractures. Glucocorticoid-induced osteoporosis (GIOP) is a common secondary cause of osteoporosis in adults. Despite availability of clear evidence and international guidelines for the prevention of GIOP, a large treatment gap remains. In this narrative review, the Belgian Bone Club (BBC) updates its 2006 consensus recommendations for the prevention and treatment of GIOP in adults. The pathophysiology of GIOP is multifactorial. The BBC strongly advises non-pharmacological measures including physical exercise, smoking cessation and avoidance of alcohol abuse in all adults at risk for osteoporosis. Glucocorticoids are associated with impaired intestinal calcium absorption; the BBC therefore strongly recommend sufficient calcium intake and avoidance of vitamin D deficiency. We recommend assessment of fracture risk, taking age, sex, menopausal status, prior fractures, glucocorticoid dose, other clinical risk factors and bone mineral density into account. Placebo-controlled randomized controlled trials have demonstrated the efficacy of alendronate, risedronate, zoledronate, denosumab and teriparatide in GIOP. We suggest monitoring by dual-energy X-ray absorptiometry (DXA) and vertebral fracture identification one year after glucocorticoid initiation. The trabecular bone score might be considered during DXA monitoring. Extended femur scans might be considered at the time of DXA imaging in glucocorticoid users on long-term (≥ 3 years) antiresorptive therapy. Bone turnover markers may be considered for monitoring treatment with anti-resorptive or osteoanabolic drugs in GIOP. Although the pathophysiology of solid organ and hematopoietic stem cell transplantation-induced osteoporosis extends beyond GIOP alone, the BBC recommends similar evaluation, prevention, treatment and follow-up principles in these patients. Efforts to close the treatment gap in GIOP and implement available effective fracture prevention strategies into clinical practice in primary, secondary and tertiary care are urgently needed.
糖皮质激素是一种有效的免疫调节剂,广泛用于多种炎症性疾病以及移植受者。然而,医源性和内源性糖皮质激素过多也会引起多种副作用,包括骨质疏松症和骨折风险增加。糖皮质激素诱导的骨质疏松症(GIOP)是成人骨质疏松症的常见继发性原因。尽管有明确的证据和国际指南用于预防 GIOP,但仍存在较大的治疗差距。在本叙述性综述中,比利时骨俱乐部(BBC)更新了其 2006 年关于成人 GIOP 的预防和治疗的共识建议。GIOP 的病理生理学是多因素的。BBC 强烈建议所有有骨质疏松风险的成年人采取非药物措施,包括体育锻炼、戒烟和避免酗酒。糖皮质激素可导致肠道钙吸收受损;因此,BBC 强烈建议摄入足够的钙并避免维生素 D 缺乏。我们建议评估骨折风险,考虑年龄、性别、绝经状态、既往骨折、糖皮质激素剂量、其他临床危险因素和骨密度。安慰剂对照的随机对照试验已经证明了阿仑膦酸钠、利塞膦酸钠、唑来膦酸、地舒单抗和特立帕肽在 GIOP 中的疗效。我们建议在开始使用糖皮质激素后一年通过双能 X 线吸收法(DXA)监测和识别椎体骨折。在长期(≥ 3 年)使用抗吸收药物的糖皮质激素使用者的 DXA 监测中,可以考虑使用骨小梁评分。在长期(≥ 3 年)使用抗吸收药物的糖皮质激素使用者的 DXA 成像时,可以考虑进行扩展股骨扫描。骨转换标志物可用于监测 GIOP 中抗吸收或成骨药物的治疗。尽管实体器官和造血干细胞移植诱导的骨质疏松症的病理生理学不仅限于 GIOP,但 BBC 建议在这些患者中采用类似的评估、预防、治疗和随访原则。迫切需要努力缩小 GIOP 中的治疗差距,并将现有的有效骨折预防策略纳入初级、二级和三级保健的临床实践中。