Pediatr Allergy Immunol. 1998 Aug;9(3):116-24.
There is a common progression known as the allergic march from atopic dermatitis to allergic asthma. Cetirizine has several antiallergic properties that suggest a potential effect on the development of airway inflammation and asthma in infants with atopic dermatitis.
Over a two year period, 817 infants aged one to two years who suffered from atopic dermatitis and with a history of atopic disease in a parent or sibling were included in the ETAC (Early Treatment of the Atopic Child) trial, a multi-country, double-blind, randomised, placebo-controlled trial. The infants were treated for 18 months with either cetirizine (0.25mg/ kg b.i.d.) or placebo. The number of infants who developed asthma was compared between the two groups. Clinical and biological assessments including analysis of total and specific IgE antibodies were performed.
In the placebo group, the relative risk (RR) for developing asthma was elevated in patients with a raised level of total IgE (> or = 30 kU/l) or specific IgE (> or = 0.35 kUA/l) for grass pollen, house dust mite or cat dander (RR between 1.4 and 1.7). Compared to placebo, cetirizine significantly reduced the incidence of asthma for patients sensitised to grass pollen (RR = 0.5) or to house dust mite (RR = 0.6). However, in the population that included all infants with normal and elevated total or specific IgE (intention-to-treat - ITT), there was no difference between the numbers of infants developing asthma while receiving cetirizine or placebo. The adverse events profile was similar in the two treatment groups.
Raised total IgE level and raised specific IgE levels to grass pollen, house dust mite or cat dander were predictive of subsequent asthma. Cetirizine halved the number of patients developing asthma in the subgroups sensitised to grass pollen or house dust mite (i.e. 20% of the study population). In view of the proven safety of the drug, we propose this treatment as a primary pharmacological intervention strategy to prevent the development of asthma in specifically sensitised infants with atopic dermatitis.
有一种常见的病程进展,即从特应性皮炎发展为过敏性哮喘的“过敏进程”。西替利嗪具有多种抗过敏特性,这表明其可能对患有特应性皮炎的婴儿气道炎症和哮喘的发展产生影响。
在一项多国、双盲、随机、安慰剂对照试验——“特应性儿童早期治疗”(ETAC)试验中,纳入了817名年龄在1至2岁、患有特应性皮炎且父母或兄弟姐妹有特应性疾病病史的婴儿。这些婴儿接受了为期18个月的西替利嗪(0.25mg/kg,每日两次)或安慰剂治疗。比较了两组中患哮喘婴儿的数量。进行了包括总IgE和特异性IgE抗体分析在内的临床和生物学评估。
在安慰剂组中,总IgE水平升高(≥30 kU/l)或对草花粉、屋尘螨或猫皮屑的特异性IgE水平升高(≥0.35 kUA/l)的患者患哮喘的相对风险(RR)升高(RR在1.4至1.7之间)。与安慰剂相比,西替利嗪显著降低了对草花粉致敏(RR = 0.5)或对屋尘螨致敏(RR = 0.6)患者的哮喘发病率。然而,在包括所有总IgE或特异性IgE正常和升高的婴儿的总体人群(意向性治疗——ITT)中,接受西替利嗪或安慰剂治疗的婴儿患哮喘的数量没有差异。两个治疗组的不良事件情况相似。
总IgE水平升高以及对草花粉、屋尘螨或猫皮屑的特异性IgE水平升高可预测随后的哮喘。西替利嗪使对草花粉或屋尘螨致敏的亚组(即研究人群的20%)中患哮喘的患者数量减半。鉴于该药物已证实的安全性,我们建议将这种治疗作为一种主要的药物干预策略,以预防患有特应性皮炎的特定致敏婴儿哮喘的发展。