Cited by 1,294Bone health and osteoporosis researchMenopause: Health Impacts and TreatmentsHIV-related health complications and treatments

The epidemiology of corticosteroid-induced osteoporosis: a meta-analysis

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Staa, T. P. van, Staa, T. P. van, Staa, T. P. van, Leufkens, H. G. M., Cooper, C.·2002·Osteoporosis International

Abstract

Studies of oral corticosteroid dose and loss of bone mineral density have reported inconsistent results. In this meta-analysis, we used information from 66 papers on bone density and 23 papers on fractures to examine the effects of oral corticosteroids on bone mineral density and risk of fracture. Strong correlations were found between cumulative dose and loss of bone mineral density and between daily dose and risk of fracture. The risk of fracture was found to increase rapidly after the start of oral corticosteroid therapy (within 3 to 6 months) and decrease after stopping therapy. The risk remained independent of underlying disease, age and gender. We conclude that oral corticosteroid treatment using more than 5 mg (of prednisolone or equivalent) daily leads to a reduction in bone mineral density and a rapid increase in the risk of fracture during the treatment period. Early use of preventive measures against corticosteroid-induced osteoporosis is recommended.

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Crossref · 10.1007/s001980200108

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  • Sex matching is essential since human male/female differences have been found in total brain volume, gray matter brain volume in specific regions and brain connectivity; sexual dimorphism of the brain has also been found during childhood.

    “Moreover, sex matching is essential since human male/female differences have been found in total brain volume (697), gray matter brain volume in specific regions (698) and brain connectivity (699); sexual dimorphism of the brain has also been found during childhood (700)(reviewed in (689)).”

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Authors
Staa, T. P. V., Staa, T. P. V., Staa, T. P. V., Leufkens, H. G. M., & Cooper, C.
Affiliations
  • Utrecht University (NL)
  • Southampton General Hospital (GB)
Venue
Osteoporosis International
Published
2002-10-01
Volume
13
Issue
10
Pages
777-787
ISSN
  • 0937-941X (ISSN-L)
  • 1433-2965
OpenAlex
W2124011858
Cited by
1,294
References
4
Citations by year
2026: 34 · 2025: 45 · 2024: 54 · 2023: 47 · 2022: 62 · 2021: 84 · 2020: 54 · 2019: 68 · 2018: 58 · 2017: 72 · 2016: 52 · 2015: 58 · 2014: 51 · 2013: 52 · 2012: 47
FWCI
29.89
Type
journal article
Language
en
Open access
Locations
  • Osteoporosis International (publishedVersion)
  • PubMed (publishedVersion)
  • Research Explorer (The University of Manchester) (publishedVersion)
  • Utrecht University Repository (Utrecht University) (submittedVersion, other-oa)
  • ePrints Soton (University of Southampton) (submittedVersion)
Topics
  • Health Sciences › Medicine › Orthopedics and Sports Medicine › Bone health and osteoporosis research
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Menopause: Health Impacts and Treatments
  • Health Sciences › Medicine › Emergency Medicine › HIV-related health complications and treatments
Keywords
corticosteroid-induced osteoporosis, oral corticosteroids, bone mineral density, fracture risk, cumulative dose, prednisolone, dose-response relationship, osteoporosis prevention
MeSH terms
Aged, Cross-Sectional Studies, Dose-Response Relationship, Drug, Female, Glucocorticoids, Humans, Longitudinal Studies, Male, Middle Aged, Osteoporosis, Prednisolone, Risk Factors, Time Factors, Bone Density, Fractures, Bone

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