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Meta-Analysis
. 2010 Jun;18(6):700-6.
doi: 10.1038/ejhg.2009.224. Epub 2010 Jan 13.

Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy

Affiliations
Meta-Analysis

Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy

Emmanuelle Bouzigon et al. Eur J Hum Genet. 2010 Jun.

Abstract

Asthma is caused by a heterogeneous combination of environmental and genetic factors. In the context of GA2LEN (Global Allergy and Asthma European Network), we carried out meta-analyses of almost all genome-wide linkage screens conducted to date in 20 independent populations from different ethnic origins (>or=3024 families with >or=10 027 subjects) for asthma, atopic asthma, bronchial hyper-responsiveness and five atopy-related traits (total immunoglobulin E level, positive skin test response (SPT) to at least one allergen or to House Dust Mite, quantitative score of SPT (SPTQ) and eosinophils (EOS)). We used the genome scan meta-analysis method to assess evidence for linkage within bins of traditionally 30-cM width, and explored the manner in which these results were affected by bin definition. Meta-analyses were conducted in all studies and repeated in families of European ancestry. Genome-wide evidence for linkage was detected for asthma in two regions (2p21-p14 and 6p21) in European families ascertained through two asthmatic sibs. With regard to atopy phenotypes, four regions reached genome-wide significance: 3p25.3-q24 in all families for SPT and three other regions in European families (2q32-q34 for EOS, 5q23-q33 for SPTQ and 17q12-q24 for SPT). Tests of heterogeneity showed consistent evidence of linkage of SPTQ to 3p11-3q21, whereas between-study heterogeneity was detected for asthma in 2p22-p13 and 6p21, and for atopic asthma in 1q23-q25. This large-scale meta-analysis provides an important resource of information that can be used to prioritize further fine-mapping studies and also be integrated with genome-wide association studies to increase power and better interpret the outcomes of these studies.

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Figures

Figure 1
Figure 1
Meta-analysis results for genome-wide linkage scans of asthma and asthma-related phenotypes in ALL families. Minus Log10 P-values of weighted summed ranks (vertical axis) are plotted against the bin location (horizontal axis), with a single point plotted for each bin. Thresholds for genome-wide, suggestive and nominal significance are shown. Each phenotype is represented with a different colour: asthma (blue), atopic asthma (orange), BHR (black), IgE (green), SPT (red), SPT to HDM (brown), SPTQ (magenta) and eosinophils (cyan).

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References

    1. Wenzel SE. Asthma: defining of the persistent adult phenotypes. Lancet. 2006;368:804–813. - PubMed
    1. Steinke JW, Rich SS, Borish L. 5. Genetics of allergic disease. J Allergy Clin Immunol. 2008;121:S384–S387. - PubMed
    1. Vercelli D. Discovering susceptibility genes for asthma and allergy. Nat Rev Immunol. 2008;8:169–182. - PubMed
    1. Roeder K, Bacanu SA, Wasserman L, Devlin B. Using linkage genome scans to improve power of association in genome scans. Am J Hum Genet. 2006;78:243–252. - PMC - PubMed
    1. Denham S, Koppelman GH, Blakey J, et al. Meta-analysis of genome-wide linkage studies of asthma and related traits. Respir Res. 2008;9:38. - PMC - PubMed

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