H. Nagata et al., Association between nasal allergy and a coding variant of the Fc epsilon-RI beta gene Glu237Gly in a Japanese population, HUM GENET, 109(3), 2001, pp. 262-266
The gene for the beta -chain of the high-affinity receptor for IgE (Fc epsi
lon RI beta) has been proposed as a candidate gene for atopy. A coding vari
ant Glu237Gly has been studied in various populations with asthma and atopy
, and the results were controversial for association of the variant with at
opy/asthma. Because nasal allergy is a more common atopic disease and shows
less remission than asthma, we analyzed whether the Glu237Gly variant is c
orrelated with nasal allergy. The study enrolled 233 patients with nasal al
lergy and 100 control subjects. Further, three subgroups were selected: pat
ients with perennial nasal allergy (n= 149), Japanese cedar pollinosis (n=
189). and allergy to multiple allergens (n=45). The allele frequency of Gly
237 in the controls and patients was 0.14 and 0.20, and the frequency of Gl
y237-positive subjects was 0.23 and 0.356, respectively. There was a signif
icant association between Gly237-positivity and nasal allergy, perennial na
sal allergy, Japanese cedar pollinosis, and allergy to multiple allergens.
Among all 333 subjects we observed a significant relationship between Gly23
7 and elevated levels of serum total IgE (>250 IU/ml) and very high IgE (>1
000 IU/ml). Among patients positive for a specific IgE, Gly237 was signific
antly associated with high IgE for house dust, mite, and Japanese cedar pol
len. These results suggest that the Glu237Gly variant of the Fc,Fc epsilon
RI beta gene is involved in the development of nasal allergy through the pr
ocess for the production of both specific and nonspecific IgE antibodies.