Dose-response for adrenal suppression with hydrofluoroalkane formulations of fluticasone propionate and beclomethasone dipropionate

Stephen J Fowler, Linda Orr, Andrew M. Wilson, Erika J Sims, Brian J Lipworth

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    25 Citations (Scopus)

    Abstract

    Aims With the recent introduction of hydrofluoroalkane (HFA) inhalers it is important to know the relative systemic safety profiles of inhaled corticosteroids. We therefore decided to compare systemic bioavailability of HFA-beclomethasone dipropionate (BDP) vs HFA-fluticasone propionate (FP).

    Methods Sixteen healthy volunteers were randomised in placebo-controlled single blind cross-over fashion to receive 3 weeks with HFA-FP or HFA-BDP, given as 1 week cumulative doubling doses (nominal ex-valve) of 500, 1000 and 2000 µg day-1, with a 1 week placebo run-in and wash-out. Overnight (22.00 h to 08.00 h) and early morning (08.00 h) urinary cortisol/creatinine excretion and 08.00 h serum cortisol were measured after each placebo and dosing period. All data were log-transformed to normalize their distribution.

    Results Urine and serum cortisol were suppressed by 2000 µg FP and BDP vs placebo and by 1000 µg BDP vs placebo for urinary cortisol/creatinine (P < 0.05). Overnight urinary cortisol/creatinine ratio (the primary endpoint) was suppressed more by 1000 µg BDP vs 1000 µg FP (P < 0.05), amounting to a geometric mean fold difference (95% CI) of 1.64 (1.04–2.56). There were also more individual low values less than 3 nmol mmol-1 with BDP than FP at 1000 µg: n = 8/16 vs n = 2/16 (P < 0.05).

    Conclusions There was dose-related suppression of corrected urinary cortisol/creatinine with the HFA formulations of BDP and FP. Suppression of overnight urinary cortisol/creatinine ratio was significantly greater with HFA-BDP than HFA-FP at 1000 µg. This suggests that the greater glucocorticoid potency of HFA-FP may be offset by the greater lung bioavailability of HFA-BDP
    Original languageEnglish
    Pages (from-to)93-5
    Number of pages3
    JournalBritish Journal of Clinical Pharmacology
    Volume52
    Issue number1
    DOIs
    Publication statusPublished - 2001

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