Atopic dermatitis is known to be associated with the subsequent development
of asthma in young children. As cetirizine has confirmed anti-allergic and
potential anti-inflammatory properties, it was only natural to consider th
e use of this agent in the primary prevention of asthma. Methods: Over a 2-
year period, 817 infants aged 1 to 2 years with atopic dermatitis and a clo
se family history of atop): were included in the multicentre, randomized do
uble-blind placebo-controlled ETAC study (Early Treatment of the Atopic Chi
ld). The main criterion was comparison of the incidence of asthma in the 2
groups. The course of clinical symptoms and laboratory signs, including tot
al and specific serum IgE assays in relation to certain allergens, was also
followed. Results: The relative risk (RR) of developing asthma in the plac
ebo group was high in infants with high level of total (> 30 KIU/l) or spec
ific serum IgE (> 0.358 KIU/l) directed against grass pollens, house dust m
ites and cat allergens (RR between 1.4 and 1.7). In comparison, cetirizine
significantly reduced the incidence of asthma in infants sensitized to gras
s pollens (RR = 0.5) or house dust mires (RR = 0.6). However no global diff
erence was demonstrated between the 2 groups concerning the development of
asthma. Safety was the same in the 2 groups. Conclusion: A high level of to
tal serum IgE and specific IgE directed against grass pollens, house dust m
ites and cat allergens was predictive of the subsequent development of asth
ma. Cetirzine reduced this incidence by one half in comparison with placebo
in infants sensitized to grass pollens and house dust mites. Cetirizine ca
ll therefore be proposed as primary prevention of asthma in these subjects
with atopic dermatitis and a family history of allergy.