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Journal ArticleDOI

Prevalence of oral glucocorticoid usage in the United States: a general population perspective.

Robert A. Overman, +2 more
- 01 Feb 2013 - 
- Vol. 65, Iss: 2, pp 294-298
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TLDR
This study aimed to estimate the prevalence of glucocorticoid use, duration of use, and concomitant use of antiosteoporosis pharmaceuticals in the US population age ≥20 years.
Abstract
Objective There is little information on oral glucocorticoid use in the general US population. Previously, there have been published estimates of glucocorticoid use in countries outside of the US. This study aimed to estimate the prevalence of glucocorticoid use, duration of use, and concomitant use of antiosteoporosis pharmaceuticals in the US population age ≥20 years. Methods Data from 5 cycles (1999–2008) of the National Health and Nutrition Examination Survey (NHANES) were used to provide nationally representative weighted estimates. Oral glucocorticoids and concomitant use of antiosteoporosis pharmaceuticals (bisphosphonates, calcitonin, calcium, hormone replacement therapies, teriparatide, and vitamin D) were analyzed. Results There were 356 NHANES respondents ages ≥20 years who reported use of an oral glucocorticoid in the combined cycles between 1999 and 2008. The weighted prevalence of oral glucocorticoid use was 1.2% (95% confidence interval [95% CI] 1.1–1.4) from 1999–2008, corresponding to 2,513,259 persons in the US. The mean duration of oral glucocorticoid use was 1,605.7 days (95% CI 1,261.2–1,950.1), and 28.8% (95% CI 22.2–35.4) of oral glucocorticoid users reported use for ≥5 years. Concomitant use of a bisphosphonate was reported by 8.6% (95% CI 5.1–11.7) of oral glucocorticoid users, and 37.9% (95% CI 31.7–44.0) reported usage of any antiosteoporosis pharmaceutical. Conclusion Based on NHANES data from 1999–2008, it is estimated that the prevalence of glucocorticoid use in the US is 1.2%, with a long duration of use and infrequent use of antiosteoporotic medications compared to other estimates.

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The human stress response.

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Glucocorticoid-induced osteoporosis: an update.

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11β-HSD1 is the major regulator of the tissue-specific effects of circulating glucocorticoid excess.

TL;DR: In this paper, 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) was found to be critical to developing the phenotype of Cushing syndrome.
References
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Journal ArticleDOI

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

TL;DR: It is concluded 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.
Journal ArticleDOI

Recommendations for the Prevention and Treatment of Glucocorticoid-Induced Osteoporosis

TL;DR: Treatment with a bisphosphonate is recommended to prevent bone loss in all men and postmenopausal women in whom long-term glucocorticoid treatment at > or =5 mg/day is being initiated, as well as in men andPost menopausal women receiving long- term glucocORTicoids in whom the BMD T-score at either the lumbar spine or the hip is below normal.
Journal ArticleDOI

Estimating hip fracture morbidity, mortality and costs.

TL;DR: To estimate lifetime morbidity, mortality, and costs from hip fracture incorporating the effect of deficits in activities of daily living, a large number of patients with hip fracture have had at least one hip replacement.
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