BMC Musculoskeletal Disorders | |
The correct prednisone starting dose in polymyalgia rheumatica is related to body weight but not to disease severity | |
Roberto Caporali1  Carlomaurizio Montecucco1  Massimiliano Parodi2  Marco A Cimmino2  | |
[1] IRCCS Policlinico S.Matteo, Pavia, Italy;Clinica Reumatologica, Dipartimento di Medicina Interna, Università di Genova, Viale Benedetto XV, 6, 16132 Genova, Italy | |
关键词: ultrasonography; glucocorticoid; prednisone; polymyalgia rheumatica; | |
Others : 1158511 DOI : 10.1186/1471-2474-12-94 |
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received in 2011-01-26, accepted in 2011-05-14, 发布年份 2011 | |
【 摘 要 】
Background
the mainstay of treatment of polymyalgia rheumatica (PMR) is oral glucocorticoids, but randomized controlled trials of treatment are lacking. As a result, there is no evidence from controlled studies on the efficacy of different initial doses or glucocorticoid tapering. The aim of this study is to test if 12.5 mg prednisone/day is an adequate starting dose in PMR and to evaluate clinical predictors of drug response.
Methods
60 consecutive PMR patients were treated with a starting dose of 12,5 mg/day prednisone. Clinical, laboratory, and, in a subset of 25 patients, ultrasonographic features were recorded as possible predictors of response to prednisone. Remission was defined as disappearance of at least 75% of the signs and symptoms of PMR and normalization of ESR and CRP within the first month, a scenario allowing steroid tapering.
Results
47/60 (78.3%) patients responded to 12.5 mg of prednisone after a mean interval of 6.6 ± 5.2 days. In univariate analysis, body weight and gender discriminated the two groups. In multivariate analysis, the only factor predicting a good response was low weight (p = 0.004); the higher response rate observed in women was explained by their lower weight. The mean prednisone dose per kg in the responders was 0.19 ± 0.03 mg in comparison with 0.16 ± 0.03 mg for non responders (p = 0.007).
Conclusions
12.5 mg prednisone is a sufficient starting dose in ¾ of PMR patients. The main factor driving response to prednisone in PMR was weight, a finding that could help in the clinical care of PMR patients and in designing prospective studies of treatment.
Trial Registration
ClinicalTrials.gov: NCT01169597
【 授权许可】
2011 Cimmino et al; licensee BioMed Central Ltd.
【 预 览 】
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20150408021613962.pdf | 218KB | download | |
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Figure 1. | 16KB | Image | download |
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