Becker Allan B, Kuznetsova Olga, Vermeulen J, Soto-Quiros Manuel E, Young Betty, Reiss Theodore F, Dass S Balachandra, Knorr Barbara A
Section of Allergy and Clinical Immunology, Department of Pediatrics and Child Health, University of Manitoba, Winnipeg, Canada.
Ann Allergy Asthma Immunol. 2006 Jun;96(6):800-7. doi: 10.1016/s1081-1206(10)61342-7.
Antileukotrienes and inhaled corticosteroids are asthma controller agents widely used in the treatment of pediatric asthma.
To evaluate the effects of montelukast and beclomethasone on linear growth in prepubertal asthmatic children for 1 year.
This was a 30-center study of boys (6.4-9.4 years old) and girls (6.4-8.4 years old) at Tanner stage I with mild, persistent asthma. After a placebo run-in period, 360 patients were randomized in equal ratios to double-blind, double-dummy treatment with 5 mg of montelukast, 200 microg of beclomethasone twice daily (positive control), or placebo for 56 weeks; 90% of the patients completed the study. The primary end point was linear growth velocity, measured using a stadiometer.
Linear growth rates were similar between the montelukast and placebo groups; the mean difference for the year was 0.03 cm. The mean growth rate with beclomethasone was significantly less than with placebo (-0.78 cm) or montelukast (0.81 cm) (P < .001 for both). Median percentage of days with beta-agonist use was greater with placebo (14.58%) vs montelukast (10.55%) or beclomethasone (6.65%) (P < .05 for all). More patients used oral corticosteroid rescue with placebo (34.7%) than with montelukast (25.0%) or beclomethasone (23.5%). An imbalance in bone marker levels was seen with beclomethasone but not with montelukast.
In prepubertal asthmatic children, montelukast did not affect linear growth, whereas the growth rate with beclomethasone was significantly decreased during 1 year of treatment.
抗白三烯药物和吸入性糖皮质激素是广泛用于治疗儿童哮喘的哮喘控制药物。
评估孟鲁司特和倍氯米松对青春期前哮喘儿童1年线性生长的影响。
这是一项在30个中心开展的研究,研究对象为坦纳I期、患有轻度持续性哮喘的6.4 - 9.4岁男孩和6.4 - 8.4岁女孩。经过安慰剂导入期后,360例患者按等比例随机分为双盲、双模拟治疗组,分别接受5毫克孟鲁司特、每日两次200微克倍氯米松(阳性对照)或安慰剂治疗56周;90%的患者完成了研究。主要终点是使用身高计测量的线性生长速度。
孟鲁司特组和安慰剂组的线性生长速率相似;一年的平均差异为0.03厘米。倍氯米松治疗的平均生长速率显著低于安慰剂组(-0.78厘米)或孟鲁司特组(0.81厘米)(两者P均<0.001)。使用β受体激动剂的天数中位数,安慰剂组(14.58%)高于孟鲁司特组(10.55%)或倍氯米松组(6.65%)(所有P均<0.05)。与孟鲁司特组(25.0%)或倍氯米松组(23.5%)相比,更多使用安慰剂的患者需要口服糖皮质激素进行急救(34.7%)。倍氯米松组出现骨标志物水平失衡,而孟鲁司特组未出现。
在青春期前哮喘儿童中,孟鲁司特不影响线性生长,而在1年的治疗期间,倍氯米松治疗的生长速率显著降低。