Background: Atopic disorders, including asthma, are very prevalent affectin
g up to 40% of populations, and their incidence is on the rise Although env
ironmental factors are important in the development of atopy, there is a st
rong genetic predisposition. Several genes and chromosomal regions have bee
n linked to atopy and asthma, supporting the polygenic nature of these diso
rders. IL-4 and IL-13 are T(H)2 cytokines with numerous activities that con
tribute to allergic inflammation and asthma, Both IL-4 and IL-13 use the IL
-4 receptor a chain (IL-4R alpha) as a component of their respective recept
or systems. Allelic variants of IL-4R alpha have been reported, and the R57
6IL-4R alpha allele was recently shown to be a risk factor for atopy:
Objective: We sought to determine whether the R576 allele was associated wi
th the prevalence or clinical severity of asthma.
Methods: We developed a rapid, reliable, PCR-based assay to screen individu
als for the R576IL-4R alpha allele and used this assay to genotype prospect
ively recruited individuals with asthma (n = 149) and control subjects (n =
57),
Results: There was a strong association of R576IL-4R alpha with the prevale
nce and clinical severity of asthma. in a prospective cohort, homozygosity
for R576 was significantly increased in individuals nith asthma (0 = 149, P
= .03; relative risk 8.2) compared with controls (n = 57). Furthermore, 1
or 2 copies R576IL-4R alpha correlated with asthma severity establishing a
genotype-phenotype relationship and suggesting a gene dosage effect
Conclusions: Thus R576IL-4R alpha acts as an allergic asthma susceptibility
and disease-modifying gene and may serve as a clinically useful marker of
asthma severity.