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Testing gene–environment interactions in the presence of confounders and mismeasured environmental exposures
Interest in investigating gene–environment (GxE) interactions has rapidly increased over the last decade. Although GxE interactions have been extremely investigated in large studies, few such effects have been identified and replicated, highlighting the need to develop statistical GxE tests with gre...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8473983/ https://www.ncbi.nlm.nih.gov/pubmed/34568916 http://dx.doi.org/10.1093/g3journal/jkab236 |
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author | Cheng, Chao Spiegelman, Donna Wang, Zuoheng Wang, Molin |
author_facet | Cheng, Chao Spiegelman, Donna Wang, Zuoheng Wang, Molin |
author_sort | Cheng, Chao |
collection | PubMed |
description | Interest in investigating gene–environment (GxE) interactions has rapidly increased over the last decade. Although GxE interactions have been extremely investigated in large studies, few such effects have been identified and replicated, highlighting the need to develop statistical GxE tests with greater statistical power. The reverse test has been proposed for testing the interaction effect between continuous exposure and genetic variants in relation to a binary disease outcome, which leverages the idea of linear discriminant analysis, significantly increasing statistical power comparing to the standard logistic regression approach. However, this reverse approach did not take into consideration adjustment for confounders. Since GxE interaction studies are inherently nonexperimental, adjusting for potential confounding effects is critical for valid evaluation of GxE interactions. In this study, we extend the reverse test to allow for confounders. The proposed reverse test also allows for exposure measurement errors as typically occurs. Extensive simulation experiments demonstrated that the proposed method not only provides greater statistical power under most simulation scenarios but also provides substantive computational efficiency, which achieves a computation time that is more than sevenfold less than that of the standard logistic regression test. In an illustrative example, we applied the proposed approach to the Veterans Aging Cohort Study (VACS) to search for genetic susceptibility loci modifying the smoking-HIV status association. |
format | Online Article Text |
id | pubmed-8473983 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-84739832021-09-27 Testing gene–environment interactions in the presence of confounders and mismeasured environmental exposures Cheng, Chao Spiegelman, Donna Wang, Zuoheng Wang, Molin G3 (Bethesda) Investigation Interest in investigating gene–environment (GxE) interactions has rapidly increased over the last decade. Although GxE interactions have been extremely investigated in large studies, few such effects have been identified and replicated, highlighting the need to develop statistical GxE tests with greater statistical power. The reverse test has been proposed for testing the interaction effect between continuous exposure and genetic variants in relation to a binary disease outcome, which leverages the idea of linear discriminant analysis, significantly increasing statistical power comparing to the standard logistic regression approach. However, this reverse approach did not take into consideration adjustment for confounders. Since GxE interaction studies are inherently nonexperimental, adjusting for potential confounding effects is critical for valid evaluation of GxE interactions. In this study, we extend the reverse test to allow for confounders. The proposed reverse test also allows for exposure measurement errors as typically occurs. Extensive simulation experiments demonstrated that the proposed method not only provides greater statistical power under most simulation scenarios but also provides substantive computational efficiency, which achieves a computation time that is more than sevenfold less than that of the standard logistic regression test. In an illustrative example, we applied the proposed approach to the Veterans Aging Cohort Study (VACS) to search for genetic susceptibility loci modifying the smoking-HIV status association. Oxford University Press 2021-07-16 /pmc/articles/PMC8473983/ /pubmed/34568916 http://dx.doi.org/10.1093/g3journal/jkab236 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Genetics Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Investigation Cheng, Chao Spiegelman, Donna Wang, Zuoheng Wang, Molin Testing gene–environment interactions in the presence of confounders and mismeasured environmental exposures |
title | Testing gene–environment interactions in the presence of confounders and mismeasured environmental exposures |
title_full | Testing gene–environment interactions in the presence of confounders and mismeasured environmental exposures |
title_fullStr | Testing gene–environment interactions in the presence of confounders and mismeasured environmental exposures |
title_full_unstemmed | Testing gene–environment interactions in the presence of confounders and mismeasured environmental exposures |
title_short | Testing gene–environment interactions in the presence of confounders and mismeasured environmental exposures |
title_sort | testing gene–environment interactions in the presence of confounders and mismeasured environmental exposures |
topic | Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8473983/ https://www.ncbi.nlm.nih.gov/pubmed/34568916 http://dx.doi.org/10.1093/g3journal/jkab236 |
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