Evidence map›Paper›PMID 37057071›Full record

ArticleFrontiers in nutrition2023

Genome-wide analysis of oxylipins and oxylipin profiles in a pediatric population.

Teresa Buckner, Randi K Johnson, Lauren A Vanderlinden, Patrick M Carry, Alex Romero, Suna Onengut-Gumuscu, Wei-Min Chen, Soojeong Kim, Oliver Fiehn, Brigitte I Frohnert and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in nutrition, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.6field-weighted citation impact, top 16% of its field
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

7 citing papers in PubMed, 8 citations in OpenAlex.

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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 at 5 institutions in 2 countries.

Teresa BucknerDepartment of Epidemiology, Colorado School of Public Health, Anschutz Medical Campus, Aurora, CO, United States.
Randi K JohnsonDepartment of Epidemiology, Colorado School of Public Health, Anschutz Medical Campus, Aurora, CO, United States.
Lauren A VanderlindenDepartment of Epidemiology, Colorado School of Public Health, Anschutz Medical Campus, Aurora, CO, United States.
Patrick M CarryDepartment of Epidemiology, Colorado School of Public Health, Anschutz Medical Campus, Aurora, CO, United States.
Alex RomeroDepartment of Biomedical Informatics, CU School of Medicine, Anschutz Medical Campus, Aurora, CO, United States.
Suna Onengut-GumuscuCenter for Public Health Genomics, University of Virginia, Charlottesville, VA, United States.
Wei-Min ChenCenter for Public Health Genomics, University of Virginia, Charlottesville, VA, United States.
Soojeong KimDepartment of Health Administration, Dongseo University, Busan, Republic of Korea.
Oliver FiehnNIH-West Coast Metabolomics Center, University of California-Davis, Davis, CA, United States.
Brigitte I FrohnertThe Barbara Davis Center for Diabetes, CU School of Medicine, Anschutz Medical Campus, Aurora, CO, United States.
Tessa CrumeDepartment of Epidemiology, Colorado School of Public Health, Anschutz Medical Campus, Aurora, CO, United States.
Wei PerngDepartment of Epidemiology, Colorado School of Public Health, Anschutz Medical Campus, Aurora, CO, United States.
Katerina KechrisDepartment of Biostatistics and Informatics, Colorado School of Public Health, Anschutz Medical Campus, Aurora, CO, United States.
Marian RewersThe Barbara Davis Center for Diabetes, CU School of Medicine, Anschutz Medical Campus, Aurora, CO, United States.
Jill M NorrisDepartment of Epidemiology, Colorado School of Public Health, Anschutz Medical Campus, Aurora, CO, United States.
Colorado School of Public Health · USUniversity of Colorado Anschutz Medical Campus · USUniversity of Virginia · USDongseo University · KRUniversity of California, Davis · US

Funding

PILOT STUDY--SUBSTRATE METABOLISM IN EXTREMELY LOW BIRTH WEIGHT INFANTSP30DK048520 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI JANINE A HIGGINS · 1995 to 2026
$32.6M
University of Colorado Anschutz Medical Campus DRCP30DK116073 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI LORI SUSSEL · 2020 to 2026
$10.8M
Natural History of Pre-Diabetic Autoimmunity (DAISY)R01DK032493 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI REWERS, MARIAN J · 1986 to 2024
$9.3M
Natural History of Pre-diabetic Autoimmunity (DAISY)R37DK032493 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI REWERS, MARIAN J · 2001 to 2010
$8.0M
Institutional Career Development CoreKL2TR002534 · NCATS · UNIVERSITY OF COLORADO DENVER · PI BURNHAM, ELLEN L · 2018 to 2022
$4.6M
NRSA Training CoreTL1TR002533 · NCATS · UNIVERSITY OF COLORADO DENVER · PI CICUTTO, LISA · 2018 to 2022
$3.0M
Nutrigenetics & -genomics of Vitamin D and Omega-3 Fatty Acids in Type 1 DiabetesR01DK104351 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI NORRIS, JILL M · 2014 to 2018
$2.9M
NCATS NIH HHS KL2 TR002534NCATS NIH HHS TL1 TR002533NIDDK NIH HHS P30 DK048520NIDDK NIH HHS P30 DK116073NIDDK NIH HHS R01 DK032493NIDDK NIH HHS R01 DK104351NIDDK NIH HHS R37 DK032493
6 · The paper itself

Abstract

Background: Oxylipins are inflammatory biomarkers derived from omega-3 and-6 fatty acids implicated in inflammatory diseases but have not been studied in a genome-wide association study (GWAS). The aim of this study was to identify genetic loci associated with oxylipins and oxylipin profiles to identify biologic pathways and therapeutic targets for oxylipins. Methods: We conducted a GWAS of plasma oxylipins in 316 participants in the Diabetes Autoimmunity Study in the Young (DAISY). DNA samples were genotyped using the TEDDY-T1D Exome array, and additional variants were imputed using the Trans-Omics for Precision Medicine (TOPMed) multi-ancestry reference panel. Principal components analysis of 36 plasma oxylipins was used to capture oxylipin profiles. PC1 represented linoleic acid (LA)- and alpha-linolenic acid (ALA)-related oxylipins, and PC2 represented arachidonic acid (ARA)-related oxylipins. Oxylipin PC1, PC2, and the top five loading oxylipins from each PC were used as outcomes in the GWAS (genome-wide significance: Results: The SNP rs143070873 was associated with (p < 5×10 Conclusion: Genetic loci involved in inflammation and oxylipin metabolism are associated with oxylipin levels.

Indexed as

genome-wide association studyinflammationlipid mediatorsoxylipinpediatricpolyunsaturated fatty acids

Identifiers

PMID37057071
PMCPMC10086335
OpenAlexW4361214545

What OpenQuestion holds

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LicenceCC BY
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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.