Feiss G, Morris R, Rom D, Mansfield L, Dockhorn R, Ellis E, Smith J A, Tobey R E
Rhone-Poulenc Rorer Central Research, Collegeville, Pa 19426-0107.
J Allergy Clin Immunol. 1992 Jun;89(6):1151-6. doi: 10.1016/0091-6749(92)90299-h.
A comparison of adrenocortical function before and after treatment with either intranasal triamcinolone acetonide aerosol (ITAA), prednisone, or placebo was done. Sixty-two male subjects with allergic rhinitis were treated for 6 weeks with either ITAA (220 or 440 micrograms/day), oral prednisone (10 mg/day), or placebo in double-blind, parallel-group fashion. Adrenocortical function was assessed by 6-hour cosyntropin stimulation before and at the end of the treatment period. The placebo-treated and two ITAA-treated groups produced no changes in adrenocortical function with treatment, and the ITAA-treated groups were not different from the placebo-treated group with mean +/- SEM changes in stimulated plasma cortisol (micrograms per deciliter) as follows: placebo, -2.68 +/- 1.77; ITAA 220 micrograms, -2.69 +/- 1.18; ITAA 440 micrograms, -2.96 +/- 1.81. The prednisone-treated group had a mean reduction in adrenocortical function (mean +/- SEM change in stimulated plasma cortisol of -19.8 +/- 1.77 micrograms/dl) that was significant (p less than 0.0001) compared with that of the placebo-treated group. The results of this study indicate that 6 weeks of treatment with 220 micrograms/day or 440 micrograms/day of ITAA has no effect on adrenocortical function, but prednisone, at a dosage of 10 mg/day for 6 weeks, produces partial adrenocortical suppression.
对使用鼻内曲安奈德气雾剂(ITAA)、泼尼松或安慰剂治疗前后的肾上腺皮质功能进行了比较。62名患有过敏性鼻炎的男性受试者以双盲、平行组方式接受了6周的治疗,分别使用ITAA(220或440微克/天)、口服泼尼松(10毫克/天)或安慰剂。在治疗期开始前和结束时,通过6小时促肾上腺皮质激素刺激试验评估肾上腺皮质功能。安慰剂治疗组和两个ITAA治疗组在治疗后肾上腺皮质功能均无变化,且ITAA治疗组与安慰剂治疗组在刺激后血浆皮质醇(微克/分升)的平均变化(平均值±标准误)方面无差异,具体如下:安慰剂组,-2.68±1.77;ITAA 220微克组,-2.69±1.18;ITAA 440微克组,-2.96±1.81。泼尼松治疗组肾上腺皮质功能平均降低(刺激后血浆皮质醇的平均变化为-19.8±1.77微克/分升),与安慰剂治疗组相比具有显著性差异(p<0.0001)。本研究结果表明,每天220微克或440微克的ITAA治疗6周对肾上腺皮质功能无影响,但泼尼松以10毫克/天的剂量治疗6周会导致部分肾上腺皮质抑制。