Evidence map›Paper›PMID 38420714›Full record

ArticleGenetic epidemiology2024

Unveiling challenges in Mendelian randomization for gene-environment interaction.

Malka Gorfine, Conghui Qu, Ulrike Peters, Li Hsu

Abstract read
In one paragraph

Article in Genetic epidemiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Article
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  5. Review
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.

Malka GorfineDepartment of Statistics and Operations Research, Tel Aviv University, Tel Aviv, Israel.
Conghui QuDivision of Public Health Sciences, Fred Hutchinson Cancer Center, Seattle, Washington, USA.
Ulrike PetersDivision of Public Health Sciences, Fred Hutchinson Cancer Center, Seattle, Washington, USA.
Li HsuDivision of Public Health Sciences, Fred Hutchinson Cancer Center, Seattle, Washington, USA.ORCID 0000-0001-8168-4712

Funding

Detection of Colorectal Cancer Susceptibility Loci Using Genome-Wide SequencingU01CA164930 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PETERS, ULRIKE · 2012 to 2015
$12.4M
Development of the Basal Telencephalic Limbic SystemR01DA020140 · NIDA · GEORGETOWN UNIVERSITY · PI CORBIN, JOSHUA G · 2006 to 2020
$7.3M
Statistical Methods for Analysis of Tumor Heterogeneity in Genetic EpidemiologyR01CA189532 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI HSU, LI · 2015 to 2023
$4.2M
Integrative Genomics into Genetic Association Studies of Blood Pressure and Stroke in African AmericansR01HL152439 · NHLBI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI HSU, LI, KOOPERBERG, CHARLES L · 2021 to 2024
$2.8M
Statistical Methods for Inferring Gene-Phenotype Associations Using Omic Data from Gene Knockout and Human Phenotype StudiesU01HG013177 · NHGRI · FRED HUTCHINSON CANCER CENTER · PI Li Hsu, ALI SHOJAIE · 2023 to 2026
$2.2M
Statistical Methods for Genetic Epidemiology StudiesR01CA195789 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI HSU, LI · 2016 to 2019
$1.6M
Israel Science Foundation (ISF) 767/21NCI NIH HHS R01 CA189532NCI NIH HHS R01 CA195789NCI NIH HHS U01 CA164930NHGRI NIH HHS U01 HG013177NHLBI NIH HHS R01 HL152439NIDA NIH HHS R01 DA020140NIH HHSTel-Aviv University Center
6 · The paper itself

Abstract

Gene-environment (GxE) interactions play a crucial role in understanding the complex etiology of various traits, but assessing them using observational data can be challenging due to unmeasured confounders for lifestyle and environmental risk factors. Mendelian randomization (MR) has emerged as a valuable method for assessing causal relationships based on observational data. This approach utilizes genetic variants as instrumental variables (IVs) with the aim of providing a valid statistical test and estimation of causal effects in the presence of unmeasured confounders. MR has gained substantial popularity in recent years largely due to the success of genome-wide association studies. Many methods have been developed for MR; however, limited work has been done on evaluating GxE interaction. In this paper, we focus on two primary IV approaches: the two-stage predictor substitution and the two-stage residual inclusion, and extend them to accommodate GxE interaction under both the linear and logistic regression models for continuous and binary outcomes, respectively. Comprehensive simulation study and analytical derivations reveal that resolving the linear regression model is relatively straightforward. In contrast, the logistic regression model presents a considerably more intricate challenge, which demands additional effort.

Indexed as

Gene-Environment InteractionGenome-Wide Association StudyMendelian Randomization AnalysisComputer SimulationGenetic VariationHumansLinear ModelsLogistic ModelsModels, GeneticPolymorphism, Single Nucleotidecolorectal cancerGWASinstrumental variableinteraction effectlinear regressionlogistic regressionmeasurement errorpolygenic risk score

Identifiers

PMID38420714
PMCPMC11197907

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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.