Chapter 13 - Combining twin-family designs with measured genetic variants to study the causes of epigenetic variation

TitleChapter 13 - Combining twin-family designs with measured genetic variants to study the causes of epigenetic variation
Publication TypeBook Chapter
Year of Publication2021
AuthorsMinică, CC, Neale, MC, Boomsma, DI, van Dongen, J
EditorLi, S, Hopper, JL
Book TitleTwin and Family Studies of Epigenetics
Series TitleTranslational Epigenetics
Volume27
Pagination239-259
PublisherAcademic Press
ISBN Number978-0-12-820951-6
KeywordsCausality, Direction of causation (DOC), DNA methylation, epigenetics, Genetic relatedness matrix (GRM), heritability, Mendelian Randomization (MR), Mendelian Randomization—direction of causation model (MR-DoC), Single nucleotide polymorphism (SNP) heritability, twins
Abstract

Classical twin and family designs can be applied to examine the contribution of genetic and environmental influences to variation in epigenetic marks. Such models can be extended to allow for more in-depth questions, such as: How much of the variation in DNA methylation is explained by methylation Quantitative Trait Loci (QTLs)? Does the contribution of genetic or environmental influences differ between males and females or between younger and older individuals? Does methylation level at CpG site X have a causal effect on trait Y and vice versa, or is the association driven by genetic pleiotropy? In this chapter, we discuss twin designs that allow to address these questions. First, we describe models that incorporate genetic relationships based on genome-wide SNP data and the application of such models to DNA methylation data from adult twins and family members. Second, we discuss the value of an integration of Mendelian Randomization (MR) with the classical twin design.

URLhttps://www.sciencedirect.com/science/article/pii/B9780128209516000077
DOI10.1016/B978-0-12-820951-6.00007-7