The Power to Detect Cultural Transmission in the Nuclear Twin Family Design With and Without Polygenic Risk Scores and in the Transmitted-Nontransmitted (Alleles) Design

Twin Res Hum Genet. 2020 Oct;23(5):265-270. doi: 10.1017/thg.2020.76. Epub 2020 Oct 16.

Abstract

We compare the power of two different approaches to detect passive genotype-environment (GE) covariance originating from cultural and genetic transmission operating simultaneously. In the traditional nuclear twin family (NTF) design, cultural transmission is estimated from the phenotypic covariance matrices of the mono- and dizygotic twins and their parents. Here, phenotyping is required in all family members. A more recent method is the transmitted-nontransmitted (T-NT) allele design, which exploits measured genetic variants in parents and offspring to test for effects of nontransmitted alleles from parents. This design requires two-generation genome-wide data and a powerful genome-wide association study (GWAS) for the phenotype in addition to phenotyping in offspring. We compared the power of both designs. Using exact data simulation, we demonstrate three points: how the power of the T-NT design depends on the predictive power of polygenic risk scores (PRSs); that when the NTF design can be applied, its power to detect cultural transmission and GE covariance is high relative to T-NT; and that, given effect sizes from contemporary GWAS, adding PRSs to the NTF design does not yield an appreciable increase in the power to detect cultural transmission. However, it may be difficult to collect phenotypes of parents and the possible importance of gene × age interaction, and secular generational effects can cause complications for many important phenotypes. The T-NT design avoids these complications.

Keywords: cultural transmission; genetic nurture; nontransmitted alleles; nuclear twin family design; power.

Publication types

  • Twin Study

MeSH terms

  • Alleles
  • Culture*
  • Gene-Environment Interaction*
  • Genome-Wide Association Study*
  • Humans
  • Models, Genetic*
  • Multifactorial Inheritance
  • Risk Factors
  • Twins, Dizygotic