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A Sparse Additive Model for High-Dimensional Interactions with an Exposure Variable

View ORCID ProfileSahir R Bhatnagar, View ORCID ProfileTianyuan Lu, Amanda Lovato, David L Olds, Michael S Kobor, Michael J Meaney, Kieran O’Donnell, Yi Yang, View ORCID ProfileCelia MT Greenwood
doi: https://doi.org/10.1101/445304
Sahir R Bhatnagar
aDepartment of Epidemiology, Biostatistics and Occupational Health, McGill University, Montréal, Canada
bDepartment of Diagnostic Radiology, McGill University, Montréal, Canada
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  • For correspondence: sahir.bhatnagar@mcgill.ca
Tianyuan Lu
cQuantitative Life Sciences, McGill University
dLady Davis Institute, Jewish General Hospital, Montréal, QC
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Amanda Lovato
eStatistics Canada, Ottawa, ON
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David L Olds
fDepartment of Pediatrics, University of Colorado School of Medicine, Denver
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Michael S Kobor
gDepartment of Medical Genetics, University of British Columbia, BC
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Michael J Meaney
hSingapore Institute for Clinical Sciences, Singapore; McGill University
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Kieran O’Donnell
iDepartment of Psychiatry, McGill University
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Yi Yang
jDepartment of Mathematics and Statistics, McGill University
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Celia MT Greenwood
aDepartment of Epidemiology, Biostatistics and Occupational Health, McGill University, Montréal, Canada
cQuantitative Life Sciences, McGill University
eStatistics Canada, Ottawa, ON
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  • ORCID record for Celia MT Greenwood
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ABSTRACT

A conceptual paradigm for onset of a new disease is often considered to be the result of changes in entire biological networks whose states are affected by a complex interaction of genetic and environmental factors. However, when modelling a relevant phenotype as a function of high dimensional measurements, power to estimate interactions is low, the number of possible interactions could be enormous and their effects may be non-linear. In this work, we introduce a method called sail for detecting non-linear interactions with a key environmental or exposure variable in high-dimensional settings which respects the strong or weak heredity constraints. We prove that asymptotically, our method possesses the oracle property, i.e., it performs as well as if the true model were known in advance. We develop a computationally efficient fitting algorithm with automatic tuning parameter selection, which scales to high-dimensional datasets. Through an extensive simulation study, we show that sail outperforms existing penalized regression methods in terms of prediction accuracy and support recovery when there are non-linear interactions with an exposure variable. We apply sail to detect non-linear interactions between genes and a prenatal psychosocial intervention program on cognitive performance in children at 4 years of age. Results show that individuals who are genetically predisposed to lower educational attainment are those who stand to benefit the most from the intervention. Our algorithms are implemented in an R package available on CRAN (https://cran.r-project.org/package=sail).

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • Included new real data analyses of NFP program and SUPPORT dataset.

  • https://cran.r-project.org/package=sail

  • https://sahirbhatnagar.com/sail/

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.
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Posted November 30, 2021.
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A Sparse Additive Model for High-Dimensional Interactions with an Exposure Variable
Sahir R Bhatnagar, Tianyuan Lu, Amanda Lovato, David L Olds, Michael S Kobor, Michael J Meaney, Kieran O’Donnell, Yi Yang, Celia MT Greenwood
bioRxiv 445304; doi: https://doi.org/10.1101/445304
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A Sparse Additive Model for High-Dimensional Interactions with an Exposure Variable
Sahir R Bhatnagar, Tianyuan Lu, Amanda Lovato, David L Olds, Michael S Kobor, Michael J Meaney, Kieran O’Donnell, Yi Yang, Celia MT Greenwood
bioRxiv 445304; doi: https://doi.org/10.1101/445304

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