Abstract

Estimates from Mendelian randomization studies of unrelated individuals can be biased due to uncontrolled confounding from familial effects. Here we describe methods for within-family Mendelian randomization analyses and use simulation studies to show that family-based analyses can reduce such biases. We illustrate empirically how familial effects can affect estimates using data from 61,008 siblings from the Nord-Trøndelag Health Study and UK Biobank and replicated our findings using 222,368 siblings from 23andMe. Both Mendelian randomization estimates using unrelated individuals and within family methods reproduced established effects of lower BMI reducing risk of diabetes and high blood pressure. However, while Mendelian randomization estimates from samples of unrelated individuals suggested that taller height and lower BMI increase educational attainment, these effects were strongly attenuated in within-family Mendelian randomization analyses. Our findings indicate the necessity of controlling for population structure and familial effects in Mendelian randomization studies.

Highlights

  • Estimates from Mendelian randomization studies of unrelated individuals can be biased due to uncontrolled confounding from familial effects

  • A similar confounding structure can be induced through dynastic effects because there is a path between the offspring instrument value and the offspring outcome value, which arises through parental inheritance

  • We have presented within-family methods for Mendelian randomization and demonstrated how confounding due to population structure and familial effects can bias Mendelian randomization studies using unrelated individuals

Read more

Summary

Introduction

Estimates from Mendelian randomization studies of unrelated individuals can be biased due to uncontrolled confounding from familial effects. Mendelian randomization is an approach that uses genetic variants as instrumental variables to estimate the causal effects of one trait (the ‘exposure’) on another (the ‘outcome’)[1,2,3,4,5]. Environmental and social factors such as assortative mating, dynastic effects, and population structure may affect the distribution of genetic variants for specific traits within populations (see Supplementary Note 1)[13,14,15,16]. If assortative mating arises due to individuals with a particular genetic predisposition selecting mates who have a particular genetically influenced phenotype, this can induce spurious genetic associations which can result in biased estimates from Mendelian randomization studies[6]. Confounding by population stratification[1], in which ancestry is correlated with both phenotypes and genotypes, was a major concern during the early development of Mendelian randomization[1]

Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call