Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Clinical Trial
. 1999 Oct;54(10):894-9.
doi: 10.1136/thx.54.10.894.

Effects of inhaled fluticasone and oral prednisolone on clinical and inflammatory parameters in patients with asthma

Affiliations
Clinical Trial

Effects of inhaled fluticasone and oral prednisolone on clinical and inflammatory parameters in patients with asthma

R J Meijer et al. Thorax. 1999 Oct.

Abstract

Background: Guidelines state that oral and inhaled corticosteroids are the cornerstone of asthma treatment. The effect of both types of treatment can be assessed by measuring lung and systemic parameters. Treatment for two weeks with either oral prednisolone (30 mg/day), high dose fluticasone propionate (2000 microg/day, FP2000), or lower dose FP (500 microg/day, FP500), both given by a dry powder inhaler, were compared.

Methods: One hundred and twenty patients with asthma were treated for two weeks in a double blind parallel group design. Lung function, asthma symptoms, airway hyperresponsiveness (PC(20) methacholine and adenosine-5'-monophosphate), sputum eosinophil and eosinophilic cationic protein (ECP) levels were measured as lung parameters. In addition, morning serum blood cortisol, blood eosinophil, and serum ECP levels were measured as systemic parameters.

Results: PC(20) methacholine and adenosine-5'-monophosphate showed significantly greater improvement with FP2000 (1.99 and 4.04 doubling concentrations (DC), respectively) than prednisolone (0.90 DC, p = 0.02; 2.15 DC, p = 0. 05) and marginally more than with FP500 (1.69 and 3.54 DC). Changes in sputum eosinophil and ECP concentrations showed similar trends; the decrease in ECP was significantly greater with FP2000 than with FP500. In contrast, the systemic parameters of steroid activity (cortisol, peripheral blood eosinophils, and serum ECP) decreased to a similar extent with FP2000 and prednisolone but significantly less with FP500.

Conclusions: Oral prednisolone (30 mg/day) was inferior to FP2000 in improving airway hyperresponsiveness to both methacholine and AMP, with similar trends in forced expiratory volume in one second (FEV(1)), sputum eosinophil and ECP concentrations. Systemic effects were similar with prednisolone and FP2000 and less with FP500.

PubMed Disclaimer

Comment in

Similar articles

Cited by

References

    1. Clin Allergy. 1988 Jul;18(4):317-21 - PubMed
    1. Thorax. 1988 May;43(5):378-84 - PubMed
    1. Am J Respir Cell Mol Biol. 1997 Nov;17(5):634-41 - PubMed
    1. Am J Respir Crit Care Med. 1997 Sep;156(3 Pt 1):744-51 - PubMed
    1. Eur Respir J. 1997 Jul;10(7):1496-9 - PubMed

Publication types

MeSH terms