Association of a STAT 6 haplotype with elevated serum IgE levels in a population based cohort of white adults

Background: Several studies have shown linkage of chromosome 12q 13 - 24 with atopy related phenotypes. Among candidate genes in this region is STAT6 ( signal transducer and activator of transcription), which is essential for Th2 cell differentiation, recruitment, and effector function. Methods: We evaluated six polymorphisms of STAT6 for evidence of associations with serum IgE levels and atopic diseases in a population based cross sectional cohort of 1407 German adults. Genotyping was performed using the matrix assisted laser desorption ionisation - time of flight mass spectrometry method. Haplotypes were estimated using the SAS/Genetics module, and population-derived IgE percentiles (50% IgE> 53 kU/l, 66% IgE> 99 kU/l and 90% IgE> 307 kU/l) were modelled as outcome variables in haplotype trend regression analysis. Results: All polymorphisms were genotyped successfully. Haplotype reconstruction revealed 8/64 possible haplotypes, reaching estimated frequencies of 1% or more. One polymorphism in intron 2 (rs324011) showed a significant association with total serum IgE ( p = 0.015). A STAT6 risk haplotype for elevated IgE showing odds ratios of 1.7 ( p = 0.015) for IgE cut-off 100 kU/l, and 1.54 ( p = 0.032), 1.6 ( p = 0.025), and 2.54 ( p = 0.007) for IgE percentiles 50%, 66%, and 90%, respectively was detected. The increased risk of this haplotype was confirmed by linear haplotype trend regression on log transformed IgE values ( p = 0.007). Analysis further revealed a risk haplotype for specific sensitisation and a risk haplotype for asthma. Conclusion: The data indicate that genetic variants within STAT6 contribute significantly to IgE regulation and manifestation of atopic diseases.