%0 Journal Article
%T Using Genetic Burden Scores for Gene
%A Erin B. Ware
%A Jacquelyn Y. Taylor
%A Jennifer A. Smith
%A Michelle L. Wright
%A Sharon L. R. Kardia
%J Biological Research For Nursing
%@ 1552-4175
%D 2019
%R 10.1177/1099800419828486
%X With the rapid advancement of omics-based research, particularly big data such as genome- and epigenome-wide association studies that include extensive environmental and clinical variables, data analytics have become increasingly complex. Researchers face significant challenges regarding how to analyze multifactorial data and make use of the findings for clinical translation. The purpose of this article is to provide a scientific exemplar for use of genetic burden scores as a data analysis method for studies with both genotype and DNA methylation data in which the goal is to evaluate associations with chronic conditions such as metabolic syndrome (MetS). This study included 739 African American men and women from the Genetic Epidemiology Network of Arteriopathy Study who met diagnostic criteria for MetS and had available genetic and epigenetic data. Genetic burden scores for evaluated genes were not significant after multiple testing corrections, but DNA methylation at 2 CpG sites (dihydroorotate dehydrogenase cg22381196 pFDR = .014; CTNNA3 cg00132141 pFDR = .043) was significantly associated with MetS after controlling for multiple comparisons. Interactions between the marginally significant CpG sites and burden scores, however, were not significant. More work is required in this area to identify intermediate biological pathways influenced by environmental, genetic, and epigenetic variation that may explain the high prevalence of MetS among African Americans. This study does serve, however, as an example of the use of the genetic burden score as an alternative data analysis approach for complex studies involving the analysis of genetic and epigenetic data simultaneously
%K genetic burden score
%K DNA methylation
%K G กม E interaction
%K African American
%K metabolic syndrome
%K Gene กม Methylation interaction
%U https://journals.sagepub.com/doi/full/10.1177/1099800419828486