Evidence map›Paper›PMID 29453499›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society2018

Screening for gene-environment (G×E) interaction using omics data from exposed individuals: an application to gene-arsenic interaction.

Maria Argos, Lin Tong, Shantanu Roy, Mekala Sabarinathan, Alauddin Ahmed, Md Tariqul Islam, Tariqul Islam, Muhammad Rakibuz-Zaman, Golam Sarwar, Hasan Shahriar and 8 more

Abstract read
In one paragraph

Article in Mammalian genome : official journal of the International Mammalian Genome Society, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Introduction to mammalian genome special issue: the combined role of genetics and environment relevant to human disease outcomes.Mammalian genome : official journal of the International Mammalian Genome Society · 2018
    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

18 authors.

Maria ArgosDivision of Epidemiology and Biostatistics, University of Illinois at Chicago, 1603 West Taylor Street, MC 923, Chicago, IL, 60612, USA. argos@uic.edu.
Lin TongDepartment of Public Health Sciences, University of Chicago, Chicago, IL, 60637, USA.
Shantanu RoyDepartment of Public Health Sciences, University of Chicago, Chicago, IL, 60637, USA.
Mekala SabarinathanDepartment of Public Health Sciences, University of Chicago, Chicago, IL, 60637, USA.
Alauddin AhmedUChicago Research Bangladesh, Dhaka, Bangladesh.
Md Tariqul IslamUChicago Research Bangladesh, Dhaka, Bangladesh.
Tariqul IslamUChicago Research Bangladesh, Dhaka, Bangladesh.
Muhammad Rakibuz-ZamanUChicago Research Bangladesh, Dhaka, Bangladesh.
Golam SarwarUChicago Research Bangladesh, Dhaka, Bangladesh.
Hasan ShahriarUChicago Research Bangladesh, Dhaka, Bangladesh.
Mahfuzar RahmanResearch and Evaluation Division, BRAC, Dhaka, Bangladesh.
Md YunusInternational Centre for Diarrhoeal Disease Research, Dhaka, Bangladesh.
Joseph H GrazianoDepartment of Environmental Health Sciences, Mailman School of Public Health, Columbia University, New York, NY, 10032, USA.
Farzana JasmineDepartment of Public Health Sciences, University of Chicago, Chicago, IL, 60637, USA.
Muhammad G KibriyaDepartment of Public Health Sciences, University of Chicago, Chicago, IL, 60637, USA.
Xiang ZhouDepartment of Biostatistics, University of Michigan School of Public Health, Ann Arbor, MI, 48109, USA.
Habibul AhsanDepartment of Public Health Sciences, University of Chicago, Chicago, IL, 60637, USA.
Brandon L PierceDepartment of Public Health Sciences, University of Chicago, Chicago, IL, 60637, USA. brandonpierce@uchicago.edu.ORCID http://orcid.org/0000-0002-7829-952X

Funding

Training CoreP42ES010349 · NIEHS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI NAVAS-ACIEN, ANA · 2000 to 2020
$53.6M
True Metal fac coreP30ES009089 · NIEHS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MATTHEW S PERZANOWSKI · 1998 to 2026
$44.7M
Occupational Safety and Health, ERC, University of Illinois at ChicagoT42OH008672 · OH · UNIVERSITY OF ILLINOIS AT CHICAGO · PI BUCHANAN, SUSAN NATHALIE · 2005 to 2025
$32.7M
Chemoprevention of arsenic-induced skin cancerR01CA107431 · NCI · UNIVERSITY OF CHICAGO · PI AHSAN, HABIBUL · 2005 to 2014
$17.3M
Pilot Program CoreP30ES027792 · NIEHS · UNIVERSITY OF CHICAGO · PI Gokhan M. Mutlu, Gail S Prins · 2017 to 2026
$13.6M
Arsenic and the Human Genome: susceptibility and response to exposure Supplement 4R35ES028379 · NIEHS · UNIVERSITY OF CHICAGO · PI PIERCE, BRANDON LEE · 2017 to 2024
$5.6M
Genetics of arsenic metabolism: fine-mapping and rare variant analysisR01ES023834 · NIEHS · UNIVERSITY OF CHICAGO · PI PIERCE, BRANDON LEE · 2014 to 2017
$2.5M
Identifying arsenic susceptibility variants using a functional screening approachR21ES024834 · NIEHS · UNIVERSITY OF CHICAGO · PI ARGOS, MARIA, PIERCE, BRANDON LEE · 2015 to 2017
$490k
Perkin-Elmer NexION-300D Inductively Coupled Mass Spectrometer (ICP-MS)S10OD016384 · OD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI GRAZIANO, JOSEPH H · 2014 to 2014
$181k
NCI NIH HHS R01 CA107431NIEHS NIH HHS P30 ES009089NIEHS NIH HHS R01 ES023834NIEHS NIH HHS R21 ES024834NIEHS NIH HHS R35 ES028379NIH HHS S10 OD016384NIOSH CDC HHS T42 OH008672
6 · The paper itself

Abstract

Identifying gene-environment interactions is a central challenge in the quest to understand susceptibility to complex, multi-factorial diseases. Developing an understanding of how inter-individual variability in inherited genetic variation alters the effects of environmental exposures will enhance our knowledge of disease mechanisms and improve our ability to predict disease and target interventions to high-risk sub-populations. Limited progress has been made identifying gene-environment interactions in the epidemiological setting using existing statistical approaches for genome-wide searches for interaction. In this paper, we describe a novel two-step approach using omics data to conduct genome-wide searches for gene-environment interactions. Using existing genome-wide SNP data from a large Bangladeshi cohort study specifically designed to assess the effect of arsenic exposure on health, we evaluated gene-arsenic interactions by first conducting genome-wide searches for SNPs that modify the effect of arsenic on molecular phenotypes (gene expression and DNA methylation features). Using this set of SNPs showing evidence of interaction with arsenic in relation to molecular phenotypes, we then tested SNP-arsenic interactions in relation to skin lesions, a hallmark characteristic of arsenic toxicity. With the emergence of additional omics data in the epidemiologic setting, our approach may have the potential to boost power for genome-wide interaction research, enabling the identification of interactions that will enhance our understanding of disease etiology and our ability to develop interventions targeted at susceptible sub-populations.

Indexed as

Gene-Environment InteractionGenetic Predisposition to DiseaseAnimalsArsenicArsenic PoisoningDNA MethylationEpistasis, GeneticGene Expression RegulationHumansPhenotypePolymorphism, Single NucleotideArsenic

Identifiers

PMID29453499
PMCPMC5908479

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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.