Characterization of the contribution of shared environmental and genetic factors to metabolic syndrome methylation heritability and familial correlations
Year: 2018
Type: article
Abstract: BACKGROUND: Transgenerational epigenetic inheritance has been posited as a possible contributor to the observed heritability of metabolic syndrome (MetS). Yet the extent to which estimates of epigenetic inheritance for DNA methylation sites are inflated by environmental and genetic covariance within families is still unclear. We applied current methods to quantify the environmental and genetic contributors to the observed heritability and familial correlations of four previously associated MetS methylation sites at three genes (CPT1A, SOCS3 and ABCG1) using real data made available through the GAW20. RESULTS: Our findings support the role of both shared environment and genetic variation in explaining the heritability of MetS and the four MetS cytosine-phosphate-guanine (CpG) sites, although the resulting heritability estimates were indistinguishable from one another. Familial correlations by type of relative pair generally followed our expectation based on relatedness, but in the case of sister and parent pairs we observed nonsignificant trends toward greater correlation than expected, as would be consistent with the role of shared environmental factors in the inflation of our estimated correlations. CONCLUSIONS: Our work provides an interesting and flexible statistical framework for testing models of epigenetic inheritance in the context of human family studies. Future work should endeavor to replicate our findings and advance these methods to more robustly describe epigenetic inheritance patterns in human populations.
Source: BMC Genetics
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $2,170
Funders: National Institutes of Health, National Heart, Lung, and Blood Institute, National Institute of General Medical Sciences, National Institute of Environmental Health Sciences, National Center for Advancing Translational Sciences, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Carolina Population Center, University of North Carolina at Chapel Hill
Awards: G3511106470, Genetic and Environmental Determinants of Triglycerides, North Carolina Translational & Clinical Sciences Institute (NC TraCS), Genomewide Association Study of Lipid Response to Fenofibrate and Dietary Fat, Carolina Population Center, Sex- and Smoking- Specific DNA Methylation Signatures of Central Adiposity Change, Genetic Analysis of Common Diseases: An Evaluation, Epigenetic Determinants of Lipid Response to Dietary Fat and Fenofibrate, G9000042165, Population Research Training, UNC Center for Environmental Health and Susceptibility, Cardiovascular Epidemiology Training Grant
OpenAlex ID: W2891585333
