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Med Sci Monit. 2014 Jan 17;20:64-71. doi: 10.12659/MSM.889754.

Epistatic effects of multiple receptor genes on pathophysiology of asthma - its limits and potential for clinical application.

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  • 1Department of Sports Medicine, Osaka City University Graduate School of Medicine, Osaka, Japan.
  • 2Department of Respiratory Medicine, Osaka City University Graduate School of Medicine, Osaka, Japan.

Abstract

To date, genome-wide association studies (GWAS) permit a comprehensive scan of the genome in an unbiased manner, with high sensitivity, and thereby have the potential to identify candidate genes for the prevalence or development of multifactorial diseases such as bronchial asthma. However, most studies have only managed to explain a small additional percentage of hereditability estimates, and often fail to show consistent results among studies despite large sample sizes. Epistasis is defined as the interaction between multiple different genes affecting phenotypes. By applying epistatic analysis to clinical genetic research, we can analyze interactions among more than 2 molecules (genes) considering the whole system of the human body, illuminating dynamic molecular mechanisms. An increasing number of genetic studies have investigated epistatic effects on the risk for development of asthma. The present review highlights a concept of epistasis to overcome traditional genetic studies in humans and provides an update of evidence on epistatic effects on asthma. Furthermore, we review concerns regarding recent trends in epistatic analyses from the perspective of clinical physicians. These concerns include biological plausibility of genes identified by computational statistics, and definition of the diagnostic label of 'physician-diagnosed asthma'. In terms of these issues, further application of epistatic analysis will prompt identification of susceptibility of diseases and lead to the development of a new generation of pharmacological strategies to treat asthma.

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PMID:
24435185
[PubMed - indexed for MEDLINE]
PMCID:
PMC3907491
Free PMC Article
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