Li J T, Ford L B, Chervinsky P, Weisberg S C, Kellerman D J, Faulkner K G, Herje N E, Hamedani A, Harding S M, Shah T
Mayo Clinic, Rochester, MN 55905, USA.
J Allergy Clin Immunol. 1999 Jun;103(6):1062-8. doi: 10.1016/s0091-6749(99)70180-6.
Although inhaled corticosteroids are widely used for the treatment of inflammation in asthma, prospective, long-term, placebo-controlled trials characterizing their systemic safety with chronic use are lacking.
This study was designed to prospectively evaluate the long-term safety of inhaled fluticasone propionate therapy.
Fluticasone propionate powder, 500 microgram, or placebo was administered twice daily by means of the Diskhaler for 104 weeks to 64 adults with mild persistent asthma in a randomized, double-blind, parallel-group study. Primary safety variables were measured at baseline and every 6 months thereafter. Although evaluation of efficacy was not an objective of this study, pulmonary function testing was performed at monthly intervals.
Two years of treatment with fluticasone propionate had no significant effects on the skeletal system. No clinically significant changes were observed in ophthalmic parameters (glaucoma and posterior subcapsular cataracts). Mean change from baseline in lumbar spine (L1 to L4 ) bone density at week 104 was not significantly different between fluticasone propionate (-0.006 +/- 0.008 g/cm2) and placebo (-0.007 +/- 0.010 g/cm2). Markers of bone formation (serum osteocalcin) and resorption (urinary N-telopeptide) did not differ significantly between treatment groups. The effects of fluticasone propionate treatment on the hypothalamic-pituitary-adrenal axis were minimal, with no alterations in morning plasma cortisol concentrations and minor but statistically significant decreases in poststimulation mean peak plasma cortisol concentrations (P =.021) and 8-hour plasma cortisol area under the curve values (P =.020) at week 104. Drug-related adverse events were primarily topical effects of inhaled corticosteroids. Pulmonary function improved significantly during 2 years of fluticasone propionate treatment.
Fluticasone propionate powder, 500 microgram twice daily for up to 2 years, was efficacious and well tolerated, with no clinically relevant effects on the hypothalamic-pituitary-adrenal axis, bone density, or ophthalmic parameters in adults with mild asthma.
尽管吸入性糖皮质激素被广泛用于治疗哮喘炎症,但缺乏前瞻性、长期、安慰剂对照试验来描述其长期使用的全身安全性。
本研究旨在前瞻性评估吸入丙酸氟替卡松治疗的长期安全性。
在一项随机、双盲、平行组研究中,对64例轻度持续性哮喘成人患者,使用Diskhaler装置,每天两次给予500微克丙酸氟替卡松粉末或安慰剂,持续104周。在基线期及之后每6个月测量主要安全变量。尽管评估疗效并非本研究的目的,但每月进行一次肺功能测试。
丙酸氟替卡松治疗两年对骨骼系统无显著影响。眼科参数(青光眼和后囊下白内障)未观察到具有临床意义的变化。在第104周时,丙酸氟替卡松组(-0.006±0.008g/cm²)和安慰剂组(-0.007±0.010g/cm²)腰椎(L1至L4)骨密度相对于基线的平均变化无显著差异。治疗组之间骨形成标志物(血清骨钙素)和骨吸收标志物(尿N-端肽)无显著差异。丙酸氟替卡松治疗对下丘脑-垂体-肾上腺轴的影响极小,在第104周时,早晨血浆皮质醇浓度无变化,刺激后平均血浆皮质醇峰值浓度有轻微但具有统计学意义的下降(P = 0.021),8小时血浆皮质醇曲线下面积值也有下降(P = 0.020)。药物相关不良事件主要是吸入性糖皮质激素的局部效应。在丙酸氟替卡松治疗的两年中,肺功能有显著改善。
对于轻度哮喘成人患者,每天两次使用500微克丙酸氟替卡松粉末,长达两年,疗效良好且耐受性佳,对下丘脑-垂体-肾上腺轴、骨密度或眼科参数无临床相关影响。