© 2003 BMJ Publishing Group & British Thoracic Society
CHRONIC OBSTRUCTIVE PULMONARY DISEASE
Prednisolone response in patients with chronic obstructive pulmonary disease: results from the ISOLDE study
1 Birmingham Heartlands Hospital, Bordesley Green East, Birmingham B9 5SS, UK
2 University Hospital Aintree, Liverpool L9 7AL, UK
3 St Georges Hospital Medical School, London SW17 0RE, UK
4 GlaxoWellcome Research and Development, Stockley Park West, Middlesex, UK
Correspondence to:
Correspondence to:
Professor P S Burge, Birmingham Heartlands Hospital, Bordesley Green East, Birmingham B9 5SS, UK;
sherwood.burge{at}heartsol.wmids.nhs.uk
Background: A trial of corticosteroids has been recommended for all patients with chronic obstructive pulmonary disease (COPD), with the subsequent "response" determining the treatment selected. This approach assumes that patients can be reliably divided into responder and non-responder groups. We have assessed whether such a separation is statistically valid, which factors influence the change in forced expiratory volume in 1 second (FEV1) after prednisolone, and whether the prednisolone response predicts 3 year changes in FEV1, health status, or number of exacerbations during placebo or fluticasone propionate treatment.
Methods: Oral prednisolone 0.6 mg/kg was given for 14 days to 524 patients with COPD before randomised treatment for 3 years with fluticasone propionate or placebo. Factors relating to change in FEV1 after prednisolone were investigated using multiple regression. The response to prednisolone was entered into separate mixed effects models of decline in FEV1 and health status during the 3 years of the study.
Results: The post-bronchodilator FEV1 increased by a mean 60 ml (CI 46 to 74) after prednisolone with a wide unimodal distribution. Current smoking was the factor most strongly associated with the change in FEV1 after prednisolone, with an increase of 35 ml in current smokers and 74 ml in confirmed ex-smokers (p<0.001). There was no relationship between the change in FEV1 after prednisolone and the response to inhaled bronchodilators, baseline FEV1, atopic status, age, or sex. The response to prednisolone, however expressed, was unrelated to the subsequent change in FEV1 over the following 3 years on either placebo or fluticasone propionate. Regression to the mean effects explained much of the apparent prednisolone response. The significant effect of treatment on decline in health status was not predicted by the prednisolone response.
Conclusion: Patients with COPD cannot be separated into discrete groups of corticosteroid responders and non-responders. Current smoking reduces the FEV1 response to prednisolone. Prednisolone testing is an unreliable predictor of the benefit from inhaled fluticasone propionate in individual patients.
Keywords: chronic obstructive pulmonary disease; prednisolone
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Thorax 2003 58: 647.
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