Author(s): Burge PS, Calverley PM, Jones PW, Spencer S, Anderson JA, et al.
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 (FEV(1)) after prednisolone, and whether the prednisolone response predicts 3 year changes in FEV(1), 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 FEV(1) after prednisolone were investigated using multiple regression. The response to prednisolone was entered into separate mixed effects models of decline in FEV(1) and health status during the 3 years of the study.
Results: The post-bronchodilator FEV(1) 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 FEV(1) 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 FEV(1) after prednisolone and the response to inhaled bronchodilators, baseline FEV(1), atopic status, age, or sex. The response to prednisolone, however expressed, was unrelated to the subsequent change in FEV(1) 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 FEV(1) response to prednisolone. Prednisolone testing is an unreliable predictor of the benefit from inhaled fluticasone propionate in individual patients.
Referred From: https://www.ncbi.nlm.nih.gov/pubmed/12885977
Author(s): Mannino DM
Author(s): Mannino DM, Homa DM, Akinbami LJ, Ford ES, Redd SC
Author(s): Xu X, Weiss ST, Rijcken B, Schouten JP
Author(s): Anthonisen NR, Connett JE, Murray RP
Author(s): Guyatt GH, Townsend M, Pugsley SO, Keller JL, Short HD, et al.
Author(s): Man WD, Mustfa N, Nikoletou D, Kaul S, Hart N, et al.
Author(s): Calverley PM, Anderson JA, Celli B, Ferguson GT, Jenkins C, et al.
Author(s): Nelson HS, Weiss ST, Bleecker ER, Yancey SW, Dorinsky PM, et al.
Author(s): Sin DD, McAlister FA, Man SF, Anthonisen NR
Author(s): Ram FS, Jones PW, Castro AA, DeBerito JA, Atallah AN, et al.
Author(s): Highland KB, Strange C, Heffner JE
Author(s): Sutherland ER, Allmers H, Ayas NT, Venn AJ, Martin RJ
Author(s): Alsaeedi, Sin DD, McAlister FA
Author(s): Burge PS, Calverley PM, Jones PW, Spencer S, Anderson JA, et al.
Author(s): Calverley P, Pauwels R, Vestbo J, Jones P, Pride N, et al.
Author(s): Mahler DA, Wire P, Horstman D, Chang C, Yates J, et al.
Author(s): Szafranski W, Cukier A, Ramirez A, Menga G, Sansores R, et al.
Author(s): Hanania NA, Darken P, Horstman D, Reisner C, Lee B, et al.
Author(s): Calverley PM, Boonsawat W, Cseke Z, Zhong N, Peterson S, et al.
Author(s): Rice KL, Rubins JB, Lebahn F, Parenti CM, Duane PG, et al.
Author(s): Decramer M, Lacquet LM, Fagard R, Rogiers P
Author(s): Decramer M, Stas KJ
Author(s): Chong J, Poole P, Leung B, Black PN
Author(s): Calverley PM, Rabe KF, Goehring UM, Kristiansen S, Fabbri LM, et al.
Author(s): Seemungal TA, Wilkinson TM, Hurst JR, Perera WR, Sapsford RJ, et al.
Author(s): He ZY, Ou LM, Zhang JQ, Bai J, Liu GN, et al.
Author(s): Wongsurakiat P, Lertakyamanee J, Maranetra KN, Jongriratanakul S, Sangkaew S
Author(s): Granger R, Walters J, Poole PJ, Lasserson TJ, Mangtani P, et al.
Author(s): Centers for Disease Control and Prevention
Author(s): Nocturnal Oxygen Therapy Trial Group
Author(s): Takabatake N, Nakamura H, Abe S, Inoue S, Hino T, et al.
Author(s): Heindl S, Lehnert M, Criee CP, Hasenfuss G, Andreas S
Author(s): Bratel T, Wennlund A, Carlstrom K
Author(s): Guyatt GH, McKim DA, Austin P, Bryan R, Norgren J, et al.
Author(s): Griffiths TL, Burr ML, Campbell IA, Lewis-Jenkins V, Mullins J, et al.
Author(s): Mehran RJ, Deslauriers J
Author(s): Moayyedi P, Congleton J, Page RL, Pearson SB, Muers MF
Author(s): Thompson WH, Nielson CP, Carvalho P, Charan NB, Crowley JJ
Author(s): Davies L, Angus RM, Calverley PM
Author(s): Niewoehner DE, Erbland ML, Deupree RH, Collins D, Gross NJ, et al.
Author(s): Maltais F, Ostinelli J, Bourbeau J, Tonnel AB, Jacquemet N, et al.
Author(s): Sethi S, Evans N, Grant BJ, Murphy TF
Author(s): Anthonisen NR, Manfreda J, Warren CP, Hershfield ES, Harding GK, et al.
Author(s): Jorgensen AF, Coolidge J, Pedersen PA, Peterson KP, Waldorff S, et al.