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Update on Glucocorticoid Induced Osteoporosisopen access

Authors
Cho, Soo-KyungSung, Yoon-Kyoung
Issue Date
Jun-2021
Publisher
대한내분비학회
Keywords
Glucocorticoids; Osteoporosis; Therapeutics
Citation
Endocrinology and Metabolism, v.36, no.3, pp.536 - 543
Indexed
SCIE
SCOPUS
KCI
Journal Title
Endocrinology and Metabolism
Volume
36
Number
3
Start Page
536
End Page
543
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/141720
DOI
10.3803/EnM.2021.1021
ISSN
2093-596X
Abstract
Glucocorticoids are used to treat many autoimmune and inflammatory diseases. However, an adverse systemic effect is a deleterious effect on bone, which may lead to glucocorticoid-induced osteoporosis, characterized by a rapid and transient increase in bone resorption and fracture risk, which may increase rapidly within 3 months of commencing oral glucocorticoids. Therefore, early risk assessment and intervention are crucial for preventing fractures in patients receiving glucocorticoids. Recent practice guidelines recommend an assessment for fracture risk in patients beginning or receiving glucocorticoids for more than 3 months, and they have suggested fracture risk assessment tool values for identifying patients who need preventive treatment. Bisphosphonates are currently the recommended first-line therapy for the prevention and treatment of glucocorticoid-induced osteoporosis. These have been shown to increase the bone mineral density in the spine and hip and to decrease the incidence of vertebral fractures. Recently, a more potent antiresorptive agent, denosumab, has been shown to increase the bone density in patients receiving glucocorticoids. Teriparatide has been shown to have a preventive effect on vertebral fractures, but not on nonvertebral fractures. In this article we aimed to providean update on glucocorticoid-induced osteoporosis by focusing on the assessment of its risk and treatment options.
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