Abstract | INTRODUCTION: METHODS: Eligible subjects with PER entered a randomized double-blind crossover study of 2 weeks of intranasal FP at 100 microg or 400 microg daily, with a 2-week placebo washout period before each randomized treatment. Measurements after each washout or treatment comprised: peak nasal inspiratory flow (PNIF) response to nasal AMP (the primary outcome), domiciliary PNIF, the mini rhinoconjunctivitis quality of life questionnaire (miniRQLQ), symptom scores, nasal nitric oxide levels and overnight urinary cortisol: creatinine ratios. RESULTS: Thirteen patients completed per protocol. Maximal PNIF response to AMP was attenuated 0.9% (95% confidence interval -7.1 to 9.0, P=NS) by FP 100 microg, and 12.9% (4.8-20.9, P=0.009) by FP 400 microg. The 400-100 microg difference was 12.0% U (2.6-21.3, P=0.049). None of the other outcomes were responsive enough to detect any significant treatment effects. The standardized response means to FP 400 microg were 81% for AMP challenge, 54% for domiciliary PNIF, 53% for miniRQLQ, 24% for symptom scores and 18% for nasal nitric oxide. No adrenal suppression was detected at either dose. CONCLUSION: FP exhibited dose-related suppression of nasal airway hyperresponsiveness to AMP challenge, but without associated detectable adrenal suppression at the higher dose. Moreover, the AMP response demonstrated the highest signal to noise ratio compared with other outcome measures in PER.
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Authors | M L Barnes, D Menzies, A R Nair, P J Hopkinson, B J Lipworth |
Journal | Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology
(Clin Exp Allergy)
Vol. 37
Issue 5
Pg. 696-703
(May 2007)
ISSN: 0954-7894 [Print] England |
PMID | 17456217
(Publication Type: Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Androstadienes
- Glucocorticoids
- Adenosine Monophosphate
- Fluticasone
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Topics |
- Adenosine Monophosphate
- Adolescent
- Adult
- Aged
- Androstadienes
(administration & dosage, adverse effects, therapeutic use)
- Cross-Over Studies
- Dose-Response Relationship, Drug
- Double-Blind Method
- Drug Monitoring
(methods)
- Female
- Fluticasone
- Glucocorticoids
(administration & dosage, adverse effects, therapeutic use)
- Humans
- Male
- Middle Aged
- Nasal Provocation Tests
(methods)
- Quality of Life
- Rhinitis, Allergic, Perennial
(drug therapy)
- Treatment Outcome
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