A Bayesian approach to gene-gene and gene-environment interactions in chronic fatigue syndrome

Pharmacogenomics. 2009 Jan;10(1):35-42. doi: 10.2217/14622416.10.1.35.

Abstract

Introduction: In the study of genomics, it is essential to address gene-gene and gene-environment interactions for describing the complex traits that involves disease-related mechanisms. In this work, our goal is to detect gene-gene and gene-environment interactions resulting from the analysis of chronic fatigue syndrome patients' genetic and demographic factors including SNPs, age, gender and BMI.

Materials & methods: We employed the dataset that was original to the previous study by the Centers for Disease Control and Prevention Chronic Fatigue Syndrome Research Group. To investigate gene-gene and gene-environment interactions, we implemented a Bayesian based method for identifying significant interactions between factors. Here, we employed a two-stage Bayesian variable selection methodology based on Markov Chain Monte Carlo approaches.

Results: By applying our Bayesian based approach, NR3C1 was found in the significant two-locus gene-gene effect model, as well as in the significant two-factor gene-environment effect model. Furthermore, a significant gene-environment interaction was identified between NR3C1 and gender. These results support the hypothesis that NR3C1 and gender may play a role in biological mechanisms associated with chronic fatigue syndrome.

Conclusion: We demonstrated that our Bayesian based approach is a promising method to assess the gene-gene and gene-environment interactions in chronic fatigue syndrome patients by using genetic factors, such as SNPs, and demographic factors such as age, gender and BMI.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age Factors
  • Bayes Theorem
  • Body Mass Index
  • Databases, Factual
  • Epigenesis, Genetic
  • Epistasis, Genetic
  • Fatigue Syndrome, Chronic / etiology*
  • Fatigue Syndrome, Chronic / genetics*
  • Gene Expression Profiling / statistics & numerical data
  • Humans
  • Markov Chains
  • Models, Genetic*
  • Polymorphism, Genetic
  • Sex Factors
  • Software