Evidence map›Paper›PMID 38039147›Full record

SynthesisBioinformatics (Oxford, England)2023

Re-analysis and meta-analysis of summary statistics from gene-environment interaction studies.

Duy T Pham, Kenneth E Westerman, Cong Pan, Ling Chen, Shylaja Srinivasan, Elvira Isganaitis, Mary Ellen Vajravelu, Fida Bacha, Steve Chernausek, Rose Gubitosi-Klug and 5 more

Abstract readMeta-Analysis
In one paragraph

Synthesis in Bioinformatics (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Genetic association analysis ofJournal of diabetes and metabolic disorders · 2025
    Article
  3. Robust Mixed Model Association Test for Gene-Environment Interactions.medRxiv : the preprint server for health sciences · 2025
    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

15 authors.

Duy T PhamHuman Genetics Center, Department of Epidemiology, School of Public Health, The University of Texas Health Science Center at Houston, Houston, TX 77030, United States.ORCID 0009-0007-2586-2087
Kenneth E WestermanDepartment of Medicine, Clinical and Translational Epidemiology Unit, Mongan Institute, Massachusetts General Hospital, Boston, MA 02114, United States.
Cong PanHuman Genetics Center, Department of Epidemiology, School of Public Health, The University of Texas Health Science Center at Houston, Houston, TX 77030, United States.
Ling ChenDepartment of Medicine, Clinical and Translational Epidemiology Unit, Mongan Institute, Massachusetts General Hospital, Boston, MA 02114, United States.
Shylaja SrinivasanDepartment of Pediatrics, University of California, San Francisco, CA 94158, United States.ORCID 0000-0002-8049-6370
Elvira IsganaitisResearch Division, Joslin Diabetes Center, Boston, MA 02115, United States.ORCID 0000-0003-3477-0305
Mary Ellen VajraveluDepartment of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA 15224, United States.
Fida BachaDepartment of Pediatrics, Baylor College of Medicine, Houston, TX 77030, United States.ORCID 0000-0002-9942-1889
Steve ChernausekDepartment of Pediatrics, The University of Oklahoma College of Medicine, Oklahoma City, OK 73117, United States.
Rose Gubitosi-KlugDepartment of Pediatrics, Case Western Reserve University, Cleveland, OH 44106, United States.
Jasmin DiversDepartment of Foundations of Medicine, New York University, New York, NY 10016, United States.
Catherine PihokerDepartment of Pediatrics, University of Washington School of Medicine, Seattle, WA 98105, United States.
Santica M MarcovinaNorthwest Lipid Metabolism and Diabetes Research Laboratories, Department of Medicine, University of Washington, Seattle, WA 98105, United States.
Alisa K ManningDepartment of Medicine, Clinical and Translational Epidemiology Unit, Mongan Institute, Massachusetts General Hospital, Boston, MA 02114, United States.
Han ChenHuman Genetics Center, Department of Epidemiology, School of Public Health, The University of Texas Health Science Center at Houston, Houston, TX 77030, United States.ORCID 0000-0002-9510-4923

Funding

SPECIAL ASSAY COREP30DK036836 · NIDDK · JOSLIN DIABETES CENTER · PI ROHIT N. KULKARNI · 1986 to 2026
$50.5M
Methods and Software for Large-Scale Gene-Environment Interaction StudiesR01HL145025 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI CHEN, HAN, MANNING, ALISA KNODLE · 2019 to 2023
$4.0M
A comprehensive approach to understanding the determinants of metformin pharmacokinetics and pharmacodynamics in youth with type 2 diabetesK23DK120932 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SRINIVASAN, SHYLAJA · 2020 to 2024
$1.1M
Improved detection of gene-diet interactions via longitudinal data, metabolomic proxies, and polygenic scoresK01DK133637 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI Kenneth E Westerman · 2022 to 2026
$749k
Pathophysiological sub-typing of pediatric type 2 diabetes based on clinical and genetic clustering methodsR03DK138213 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SRINIVASAN, SHYLAJA · 2024 to 2025
$242k
NHLBI NIH HHS R01 HL145025NIDDK NIH HHS K01 DK133637NIDDK NIH HHS K23 DK120932NIDDK NIH HHS P30 DK036836NIDDK NIH HHS R03 DK138213NIH HHS R01 HL145025
6 · The paper itself

Abstract

motivationstatistics from genome-wide association studies enable many valuable downstream analyses that are more efficient than individual-level data analysis while also reducing privacy concerns. As growing sample sizes enable better-powered analysis of gene-environment interactions, there is a need for gene-environment interaction-specific methods that manipulate and use summary statistics.

resultsWe introduce two tools to facilitate such analysis, with a focus on statistical models containing multiple gene-exposure and/or gene-covariate interaction terms. REGEM (RE-analysis of GEM summary statistics) uses summary statistics from a single, multi-exposure genome-wide interaction study to derive analogous sets of summary statistics with arbitrary sets of exposures and interaction covariate adjustments. METAGEM (META-analysis of GEM summary statistics) extends current fixed-effects meta-analysis models to incorporate multiple exposures from multiple studies. We demonstrate the value and efficiency of these tools by exploring alternative methods of accounting for ancestry-related population stratification in genome-wide interaction study in the UK Biobank as well as by conducting a multi-exposure genome-wide interaction study meta-analysis in cohorts from the diabetes-focused ProDiGY consortium. These programs help to maximize the value of summary statistics from diverse and complex gene-environment interaction studies. AVAILABILITY AND IMPLEMENTATION: REGEM and METAGEM are open-source projects freely available at https://github.com/large-scale-gxe-methods/REGEM and https://github.com/large-scale-gxe-methods/METAGEM.

Indexed as

Gene-Environment InteractionGenome-Wide Association StudyData Interpretation, StatisticalModels, StatisticalPhenotypePolymorphism, Single NucleotideSample Size

Identifiers

PMID38039147
PMCPMC10724851

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.