Application of a novel hybrid study design to explore gene-environment interactions in orofacial clefts.

Ann Hum Genet 2012 May;76(3):221-36

Division of Epidemiology, Norwegian Institute of Public Health, Oslo, Norway.

Orofacial clefts are common birth defects with strong evidence for both genetic and environmental causal factors. Candidate gene studies combined with exposures known to influence the outcome provide a highly targeted approach to detecting GxE interactions. We developed a new statistical approach that combines the case-control and offspring-parent triad designs into a "hybrid design" to search for GxE interactions among 334 autosomal cleft candidate genes and maternal first-trimester exposure to smoking, alcohol, coffee, folic acid supplements, dietary folate and vitamin A. The study population comprised 425 case-parent triads of isolated clefts and 562 control-parent triads derived from a nationwide study of orofacial clefts in Norway (1996-2001). A full maximum-likelihood model was used in combination with a Wald test statistic to screen for statistically significant GxE interaction between strata of exposed and unexposed mothers. In addition, we performed pathway-based analyses on 28 detoxification genes and 21 genes involved in folic acid metabolism. With the possible exception of the T-box 4 gene (TBX4) and dietary folate interaction in isolated CPO, there was little evidence overall of GxE interaction in our data. This study is the largest to date aimed at detecting interactions between orofacial clefts candidate genes and well-established risk exposures.

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http://dx.doi.org/10.1111/j.1469-1809.2012.00707.xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3334353PMC
May 2012
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References

(Supplied by CrossRef)
Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate
Beaty et al.
Genet Epidemiol 2011

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