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A versatile, fast and unbiased method for estimation of gene-by-environment interaction effects on biobank-scale datasets

Author

Listed:
  • Matteo Di Scipio

    (Hamilton Health Sciences and McMaster University
    McMaster University)

  • Mohammad Khan

    (Hamilton Health Sciences and McMaster University
    McMaster University)

  • Shihong Mao

    (Hamilton Health Sciences and McMaster University)

  • Michael Chong

    (Hamilton Health Sciences and McMaster University
    Vascular and Stroke Research Institute
    Michael G. DeGroote School of Medicine)

  • Conor Judge

    (Hamilton Health Sciences and McMaster University)

  • Nazia Pathan

    (Hamilton Health Sciences and McMaster University
    McMaster University)

  • Nicolas Perrot

    (Hamilton Health Sciences and McMaster University)

  • Walter Nelson

    (Hamilton Health Sciences
    University of Toronto)

  • Ricky Lali

    (Hamilton Health Sciences and McMaster University
    McMaster University)

  • Shuang Di

    (Hamilton Health Sciences
    University of Toronto)

  • Robert Morton

    (Hamilton Health Sciences and McMaster University
    Michael G. DeGroote School of Medicine)

  • Jeremy Petch

    (Hamilton Health Sciences and McMaster University
    McMaster University
    Hamilton Health Sciences
    University of Toronto)

  • Guillaume Paré

    (Hamilton Health Sciences and McMaster University
    Vascular and Stroke Research Institute
    Michael G. DeGroote School of Medicine
    McMaster University)

Abstract

Identification of gene-by-environment interactions (GxE) is crucial to understand the interplay of environmental effects on complex traits. However, current methods evaluating GxE on biobank-scale datasets have limitations. We introduce MonsterLM, a multiple linear regression method that does not rely on model specification and provides unbiased estimates of variance explained by GxE. We demonstrate robustness of MonsterLM through comprehensive genome-wide simulations using real genetic data from 325,989 individuals. We estimate GxE using waist-to-hip-ratio, smoking, and exercise as the environmental variables on 13 outcomes (N = 297,529-325,989) in the UK Biobank. GxE variance is significant for 8 environment-outcome pairs, ranging from 0.009 – 0.071. The majority of GxE variance involves SNPs without strong marginal or interaction associations. We observe modest improvements in polygenic score prediction when incorporating GxE. Our results imply a significant contribution of GxE to complex trait variance and we show MonsterLM to be well-purposed to handle this with biobank-scale data.

Suggested Citation

  • Matteo Di Scipio & Mohammad Khan & Shihong Mao & Michael Chong & Conor Judge & Nazia Pathan & Nicolas Perrot & Walter Nelson & Ricky Lali & Shuang Di & Robert Morton & Jeremy Petch & Guillaume Paré, 2023. "A versatile, fast and unbiased method for estimation of gene-by-environment interaction effects on biobank-scale datasets," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-40913-7
    DOI: 10.1038/s41467-023-40913-7
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    References listed on IDEAS

    as
    1. Guiyan Ni & Julius Werf & Xuan Zhou & Elina Hyppönen & Naomi R. Wray & S. Hong Lee, 2019. "Genotype–covariate correlation and interaction disentangled by a whole-genome multivariate reaction norm model," Nature Communications, Nature, vol. 10(1), pages 1-15, December.
    2. Clare Bycroft & Colin Freeman & Desislava Petkova & Gavin Band & Lloyd T. Elliott & Kevin Sharp & Allan Motyer & Damjan Vukcevic & Olivier Delaneau & Jared O’Connell & Adrian Cortes & Samantha Welsh &, 2018. "The UK Biobank resource with deep phenotyping and genomic data," Nature, Nature, vol. 562(7726), pages 203-209, October.
    3. Bruno Nogueira & Rian G. S. Pinheiro, 2020. "A GPU based local search algorithm for the unweighted and weighted maximum s-plex problems," Annals of Operations Research, Springer, vol. 284(1), pages 367-400, January.
    4. Zachary R. McCaw & Jacqueline M. Lane & Richa Saxena & Susan Redline & Xihong Lin, 2020. "Operating characteristics of the rank‐based inverse normal transformation for quantitative trait analysis in genome‐wide association studies," Biometrics, The International Biometric Society, vol. 76(4), pages 1262-1272, December.
    5. Peter J Castaldi & Michael H Cho & Liming Liang & Edwin K Silverman & Craig P Hersh & Kenneth Rice & Hugues Aschard, 2017. "Screening for interaction effects in gene expression data," PLOS ONE, Public Library of Science, vol. 12(3), pages 1-18, March.
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    Cited by:

    1. Nazia Pathan & Wei Q. Deng & Matteo Di Scipio & Mohammad Khan & Shihong Mao & Robert W. Morton & Ricky Lali & Marie Pigeyre & Michael R. Chong & Guillaume Paré, 2024. "A method to estimate the contribution of rare coding variants to complex trait heritability," Nature Communications, Nature, vol. 15(1), pages 1-16, December.

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