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Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses.

Authors :
Brumpton, Ben
Sanderson, Eleanor
Heilbron, Karl
Hartwig, Fernando Pires
Harrison, Sean
Vie, Gunnhild Åberge
Cho, Yoonsu
Howe, Laura D.
Hughes, Amanda
Boomsma, Dorret I.
Havdahl, Alexandra
Hopper, John
Neale, Michael
Nivard, Michel G.
Pedersen, Nancy L.
Reynolds, Chandra A.
Tucker-Drob, Elliot M.
Grotzinger, Andrew
Howe, Laurence
Morris, Tim
Source :
Nature Communications; 7/14/2020, Vol. 11 Issue 1, p1-13, 13p
Publication Year :
2020

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. Family-based study designs have been applied to resolve confounding by population stratification, dynastic effects and assortative mating in genetic association analyses. Here, Brumpton et al. describe theory and simulations for overcoming such biases in Mendelian randomization through within-family studies. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20411723
Volume :
11
Issue :
1
Database :
Complementary Index
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
144564283
Full Text :
https://doi.org/10.1038/s41467-020-17117-4