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Clinical Trial
. 1991;40(1):77-82.
doi: 10.1007/BF00315143.

Assessment of systemic effects of inhaled glucocorticosteroids: comparison of the effects of inhaled budesonide and oral prednisolone on adrenal function and markers of bone turnover

Affiliations
Clinical Trial

Assessment of systemic effects of inhaled glucocorticosteroids: comparison of the effects of inhaled budesonide and oral prednisolone on adrenal function and markers of bone turnover

B H Jennings et al. Eur J Clin Pharmacol. 1991.

Abstract

The effects of inhaled budesonide (BUD) and oral prednisolone (PRED) on markers of bone turnover and adrenal function were compared in a randomized, double-blind, double-dummy, crossover study. Twelve healthy subjects were treated for one week with 0.8, 1.6 and 3.2 mg/day BUD and 5, 10 and 20 mg/day PRED, the three doses being given in ascending order. Plasma cortisol and adrenal cortical androgens showed a significantly decreasing trend with the increasing doses of both drugs, although PRED caused a significantly greater decrease than BUD. Osteoblast function, reflected by serum osteocalcin and alkaline phosphatase was significantly reduced by PRED, but BUD had a significantly different effect as it affected only osteocalcin. Urinary hydroxyproline/creatinine, a marker of bone resorption, was not changed by either drug. The average potency ratio for equivalent systemic effects was PRED:BUD 3.9:1. During short-term treatment at equivalent anti-asthmatic doses, BUD has significantly less effect on adrenal function and bone turnover than PRED, and it may carry less risk of bone complications during long-term treatment.

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References

    1. J Steroid Biochem. 1979 Jul;11(1B):429-33 - PubMed
    1. J Clin Endocrinol Metab. 1984 Aug;59(2):228-30 - PubMed
    1. Aust N Z J Med. 1986 Jun;16(3):341-6 - PubMed
    1. J Clin Invest. 1979 Aug;64(2):655-65 - PubMed
    1. Eur J Pediatr. 1986 Apr;145(1-2):27-33 - PubMed

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