Ozbek Ozlem Yilmaz, Turktas Ipek, Bakirtas Arzu, Bideci Aysun
Pediatric Allergy and Asthma Department, Gazi University Faculty of Medicine, Ankara, Turkey.
J Pediatr Endocrinol Metab. 2006 Aug;19(8):1015-23. doi: 10.1515/jpem.2006.19.8.1015.
The aim of this study was to compare the results of low-dose (LDT) and standard-dose (SDT) ACTH tests in the assessment of adrenal function in 30 asthmatic children (mean age 9.35 +/- 1.9 years, 19 boys) who were treated with budesonide Turbohaler at conventional 400 microg or 600 microg daily doses for 8 weeks by a prospective, randomized, and open parallel study. Budesonide did not lead to any significant suppression of the hypothalamic-pituitary-adrenal (HPA) axis in either treatment group. However, when individual patient values were examined at the end point, peak cortisol concentrations after LDT were below 2 SDs of the pretreatment values in four patients (13.3%). Also, the increment in cortisol values was <200 nmol/l in all four patients. Decreased 24-hour urinary free cortisol excretion provided further evidence for HPA axis suppression in these patients. Two of these four poor responders to LDT showed normal stimulation with SDT. In conclusion, even with moderate doses and short-term use, adrenal suppression may occur in certain susceptible patients. The low-dose ACTH test is more reliable than SDT for the evaluation of such patients.
本研究旨在通过一项前瞻性、随机、开放平行研究,比较低剂量(LDT)和标准剂量(SDT)促肾上腺皮质激素(ACTH)试验在评估30例哮喘儿童(平均年龄9.35±1.9岁,19名男孩)肾上腺功能中的结果。这些儿童接受布地奈德都保治疗,常规日剂量为400微克或600微克,持续8周。在任一治疗组中,布地奈德均未导致下丘脑-垂体-肾上腺(HPA)轴出现任何显著抑制。然而,在终点时检查个体患者值时,4例患者(13.3%)在LDT后皮质醇峰值浓度低于治疗前值的2个标准差。此外,这4例患者的皮质醇值增量均<200 nmol/l。24小时尿游离皮质醇排泄减少为这些患者的HPA轴抑制提供了进一步证据。这4例对LDT反应不佳的患者中有2例对SDT刺激显示正常。总之,即使使用中等剂量且短期使用,某些易感患者仍可能发生肾上腺抑制。对于此类患者的评估,低剂量ACTH试验比SDT更可靠。