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Osteoporosis Caused by Glucocorticoids

Srđan Novak
Filip Mirić


Puni tekst: hrvatski pdf 113 Kb

str. 215-222

preuzimanja: 344

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Puni tekst: engleski pdf 113 Kb

str. 215-215

preuzimanja: 138

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Sažetak

Glucocorticoids are still seen as essential drugs in many autoimmune and inflammatory diseases, and glucocorticoid-induced osteoporosis (GIOP) is still the most common form of secondary osteoporosis. Within three months of using glucocorticoids, there is an increase in bone resorption and risk of fractures, mainly vertebral but also non-vertebral. It is necessary to constantly raise awareness about GIOP, and determining bone mineral density is recommended before starting glucocorticoid therapy. In postmenopausal women and men over 50 who are exposed to oral glucocorticoids for ≥ 3 months, it is necessary to determine facture risk using the FRAX questionnaire. Treatment uses same diagnostic criteria as for postmenopausal women (T ≤ −2.5), albeit a higher threshold is suggested (T ≤ −1.5), given that bone loss may be 10% or more during the first year of glucocorticoid use. Calcium and vitamin D are usually not sufficient for the prevention of osteoporotic fractures. The drugs of first choice are mainly bisphosphonates (alendronate, risedronate), while in some cases, especially in patients who have already suffered a fracture, teriparatide is considered due to its anabolic effect and proven reduction in the number of vertebral fractures. Denosumab can also be used as a third-line treatment.

Ključne riječi

glucocorticoids; osteoporosis; bisphosphonates; teriparatide; denosumab; FRAX

Hrčak ID:

291563

URI

https://hrcak.srce.hr/291563

Datum izdavanja:

17.1.2023.

Podaci na drugim jezicima: hrvatski

Posjeta: 1.050 *