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

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 biase...

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Autores principales: 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, Li, Shuai, Auton, Adam, Windmeijer, Frank, Chen, Wei-Min, Bjørngaard, Johan Håkon, Hveem, Kristian, Willer, Cristen, Evans, David M., Kaprio, Jaakko, Davey Smith, George, Åsvold, Bjørn Olav, Hemani, Gibran, Davies, Neil M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7360778/
https://www.ncbi.nlm.nih.gov/pubmed/32665587
http://dx.doi.org/10.1038/s41467-020-17117-4
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author 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
Li, Shuai
Auton, Adam
Windmeijer, Frank
Chen, Wei-Min
Bjørngaard, Johan Håkon
Hveem, Kristian
Willer, Cristen
Evans, David M.
Kaprio, Jaakko
Davey Smith, George
Åsvold, Bjørn Olav
Hemani, Gibran
Davies, Neil M.
author_facet 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
Li, Shuai
Auton, Adam
Windmeijer, Frank
Chen, Wei-Min
Bjørngaard, Johan Håkon
Hveem, Kristian
Willer, Cristen
Evans, David M.
Kaprio, Jaakko
Davey Smith, George
Åsvold, Bjørn Olav
Hemani, Gibran
Davies, Neil M.
author_sort Brumpton, Ben
collection PubMed
description 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.
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spelling pubmed-73607782020-07-20 Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses 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 Li, Shuai Auton, Adam Windmeijer, Frank Chen, Wei-Min Bjørngaard, Johan Håkon Hveem, Kristian Willer, Cristen Evans, David M. Kaprio, Jaakko Davey Smith, George Åsvold, Bjørn Olav Hemani, Gibran Davies, Neil M. Nat Commun Article 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. Nature Publishing Group UK 2020-07-14 /pmc/articles/PMC7360778/ /pubmed/32665587 http://dx.doi.org/10.1038/s41467-020-17117-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
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
Li, Shuai
Auton, Adam
Windmeijer, Frank
Chen, Wei-Min
Bjørngaard, Johan Håkon
Hveem, Kristian
Willer, Cristen
Evans, David M.
Kaprio, Jaakko
Davey Smith, George
Åsvold, Bjørn Olav
Hemani, Gibran
Davies, Neil M.
Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses
title Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses
title_full Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses
title_fullStr Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses
title_full_unstemmed Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses
title_short Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses
title_sort avoiding dynastic, assortative mating, and population stratification biases in mendelian randomization through within-family analyses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7360778/
https://www.ncbi.nlm.nih.gov/pubmed/32665587
http://dx.doi.org/10.1038/s41467-020-17117-4
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