Evidence map›Paper›PMID 34568916›Full record

ArticleG3 (Bethesda, Md.)2021

Testing gene-environment interactions in the presence of confounders and mismeasured environmental exposures.

Chao Cheng, Donna Spiegelman, Zuoheng Wang, Molin Wang

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Chao ChengDepartment of Biostatistics, Yale School of Public Health, New Haven, CT 06510, USA.ORCID 0000-0003-3234-5874
Donna SpiegelmanDepartment of Biostatistics, Yale School of Public Health, New Haven, CT 06510, USA.ORCID 0000-0003-4006-4650
Zuoheng WangDepartment of Biostatistics, Yale School of Public Health, New Haven, CT 06510, USA.ORCID 0000-0002-7251-3687
Molin WangDepartment of Epidemiology and Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA 02115, USA.

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Alcohol Associated Outcomes Among HIV+/- Aging VeteransU10AA013566 · NIAAA · YALE UNIVERSITY · PI JUSTICE, AMY CAROLINE · 2006 to 2010
$12.7M
Alcohol and Multisubstance Use in the Veterans Aging Cohort StudyU01AA020790 · NIAAA · YALE UNIVERSITY · PI JUSTICE, AMY CAROLINE · 2011 to 2020
$7.7M
Sex Disparities in Overall Response to ART Among HIV Infected IndividualsU24AA020794 · NIAAA · YALE UNIVERSITY · PI JUSTICE, AMY CAROLINE · 2011 to 2020
$5.5M
Statistical Methods to Account for Exposure Uncertainty in Environmental EpidemiologyR01ES026246 · NIEHS · YALE UNIVERSITY · PI SPIEGELMAN, DONNA L · 2018 to 2022
$3.1M
Novel Methods for Longitudinal Study of Gene-Environment Interplay in AlcoholismK01AA023321 · NIAAA · YALE UNIVERSITY · PI WANG, ZUOHENG · 2015 to 2019
$863k
NCATS NIH HHS UL1 TR001863NIAAA NIH HHS K01 AA023321NIAAA NIH HHS U01 AA020790NIAAA NIH HHS U10 AA013566NIAAA NIH HHS U24 AA020794NIEHS NIH HHS R01 ES026246
6 · The paper itself

Abstract

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.

Indexed as

Gene-Environment InteractionModels, GeneticCohort StudiesComputer SimulationEnvironmental ExposureHumanscomputational efficiencyconfoundersgene–environment interactionmeasurement errorrelative efficiencyreverse test

Identifiers

PMID34568916
PMCPMC8473983

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.