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Thorax 2004;59:876-882 doi:10.1136/thx.2003.014092
  • Asthma

Linkage/association study of a locus modulating total serum IgE on chromosome 14q13–24 in families with asthma

  1. A H Mansur1,
  2. D T Bishop2,
  3. S T Holgate3,
  4. A F Markham4,
  5. J F J Morrison (deceased)5
  1. 1Respiratory Department, Birmingham Heartlands Hospital, Birmingham B9 5SS, UK
  2. 2ICRF, Genetic Epidemiology Laboratory, St James’s University Hospital, Leeds, UK
  3. 3Medical Specialities (RCMB), Southampton General Hospital, Southampton, UK
  4. 4Molecular Medicine Unit, University of Leeds, Clinical Sciences Building, St James’s University Hospital, Leeds, UK
  5. 5AstraZeneca, Macclesfield, Cheshire, UK
  1. Correspondence to:
    Dr A H Mansur
    Respiratory Department, Birmingham Heartlands Hospital, Bordesley Green East, Birmingham B9 5SS, UK; adel.mansurheartsol.wmids.nhs.uk
  • Received 11 August 2003
  • Accepted 24 June 2004

Abstract

Background: A study was undertaken to validate a locus modulating total serum IgE levels on 14q13–24.

Methods: A linkage and association study was performed between total serum IgE and a panel of seven microsatellites which map to the 14q13–24 region in 69 families with asthma recruited from Leeds, UK.

Results: Non-parametric, multipoint, sib pair analysis showed no evidence of genetic linkage between the quantitative trait “log IgE” and any of the tested markers. However, a significant association was observed between locus D14S63 (14q23) and total serum IgE (p = 0.017). Allelic analysis showed an association between low total IgE and allele 157 of D14S63 (p = 0.01, OR = 0.63, 95% CI 0.44 to 0.90). Modelling of allele 157 genotypes as a continuous covariate indicated evidence of a significant inverse linear trend across the three genotypes where 157 homozygotes had the lowest mean log IgE (p = 0.045). Association of D14S63 with log IgE was confirmed in the analysis of a combined dataset of 53 families from Southampton, UK and the 69 families from Leeds (total 122 families). An association was observed at the locus level (p = 0.022) and the allelic level where allele 165 showed an association with high total IgE (p = 0.001, OR = 3.79, 95% CI 1.54 to 9.7) and allele 157 showed an association with low total IgE (p = 0.041, OR = 0.77, 95% CI 0.6 to 0.99). The transmission disequilibrium test was positive for allele 165 (p<0.05) and negative for allele 157 (p>0.05).

Conclusions: Despite the lack of linkage, the findings of this study support the previous observation of a gene(s) at 14q23 that modulates total serum IgE.

Footnotes

  • Work in the authors’ laboratory was supported by the National Asthma Campaign, MRC, Imperial Cancer Research Fund, and Yorkshire Cancer Research.

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