4.5 Article

On the use of sibling recurrence risks to select environmental factors liable to interact with genetic risk factors

Journal

EUROPEAN JOURNAL OF HUMAN GENETICS
Volume 18, Issue 1, Pages 88-94

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/ejhg.2009.119

Keywords

diabetes mellitus; type 2; epidemiologic research design; familial aggregation; genetic predisposition to disease; environmental exposure

Funding

  1. Presidency of the University Paris-Sud

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Gene-environment interactions are likely to be involved in the susceptibility to multifactorial diseases but are difficult to detect. Available methods usually concentrate on some particular genetic and environmental factors. In this paper, we propose a new method to determine whether a given exposure is susceptible to interact with unknown genetic factors. Rather than focusing on a specific genetic factor, the degree of familial aggregation is used as a surrogate for genetic factors. A test comparing the recurrence risks in sibs according to the exposure of indexes is proposed and its power is studied for varying values of model parameters. The Exposed versus Unexposed Recurrence Analysis (EURECA) is valuable for common diseases with moderate familial aggregation, only when the role of exposure has been clearly outlined. Interestingly, accounting for a sibling correlation for the exposure increases the power of EURECA. An application on a sample ascertained through one index affected with type 2 diabetes is presented where gene-environment interactions involving obesity and physical inactivity are investigated. Association of obesity with type 2 diabetes is clearly evidenced and a potential interaction involving this factor is suggested in Hispanics (P=0.045), whereas a clear gene-environment interaction is evidenced involving physical inactivity only in non-Hispanic whites (P=0.028). The proposed method might be of particular interest before genetic studies to help determine the environmental risk factors that will need to be accounted for to increase the power to detect genetic risk factors and to select the most appropriate samples to genotype. European Journal of Human Genetics (2010) 18, 88-94; doi:10.1038/ejhg.2009.119; published online 8 July 2009

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