Evidence map›Paper›PMID 33893822›Full record

ArticleDiabetologia2021

The oxylipin profile is associated with development of type 1 diabetes: the Diabetes Autoimmunity Study in the Young (DAISY).

Teresa Buckner, Lauren A Vanderlinden, Brian C DeFelice, Patrick M Carry, Katerina Kechris, Fran Dong, Oliver Fiehn, Brigitte I Frohnert, Michael Clare-Salzler, Marian Rewers and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Diabetologia, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

13 citing papers in PubMed, 21 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

11 authors at 3 institutions in 1 country.

Teresa BucknerUniversity of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Lauren A VanderlindenUniversity of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Brian C DeFeliceUniversity of California, Davis, Davis, CA, USA.
Patrick M CarryUniversity of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Katerina KechrisUniversity of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Fran DongUniversity of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Oliver FiehnUniversity of California, Davis, Davis, CA, USA.
Brigitte I FrohnertUniversity of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Michael Clare-SalzlerUniversity of Florida Health, Gainesville, FL, USA.
Marian RewersUniversity of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Jill M NorrisUniversity of Colorado Anschutz Medical Campus, Aurora, CO, USA. Jill.norris@cuanschutz.edu.
University of Colorado Anschutz Medical Campus · USUniversity of California, Davis · USUniversity of Florida Health · 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
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 TL1 TR002533NIDDK NIH HHS P30 DK048520NIDDK NIH HHS P30 DK116073NIDDK NIH HHS R01 DK032493NIDDK NIH HHS R01 DK104351
6 · The paper itself

Abstract

aims/hypothesisOxylipins are lipid mediators derived from polyunsaturated fatty acids. Some oxylipins are proinflammatory (e.g. those derived from arachidonic acid [ARA]), others are pro-resolving of inflammation (e.g. those derived from α-linolenic acid [ALA], docosahexaenoic acid [DHA] and eicosapentaenoic acid [EPA]) and others may be both (e.g. those derived from linoleic acid [LA]). The goal of this study was to examine whether oxylipins are associated with incident type 1 diabetes.

methodsWe conducted a nested case-control analysis in the Diabetes Autoimmunity Study in the Young (DAISY), a prospective cohort study of children at risk of type 1 diabetes. Plasma levels of 14 ARA-derived oxylipins, ten LA-derived oxylipins, six ALA-derived oxylipins, four DHA-derived oxylipins and two EPA-related oxylipins were measured by ultra-HPLC-MS/MS at multiple timepoints related to autoantibody seroconversion in 72 type 1 diabetes cases and 71 control participants, which were frequency matched on age at autoantibody seroconversion (of the case), ethnicity and sample availability. Linear mixed models were used to obtain an age-adjusted mean of each oxylipin prior to type 1 diabetes. Age-adjusted mean oxylipins were tested for association with type 1 diabetes using logistic regression, adjusting for the high risk HLA genotype HLA-DR3/4,DQB1*0302. We also performed principal component analysis of the oxylipins and tested principal components (PCs) for association with type 1 diabetes. Finally, to investigate potential critical timepoints, we examined the association of oxylipins measured before and after autoantibody seroconversion (of the cases) using PCs of the oxylipins at those visits.

resultsThe ARA-related oxylipin 5-HETE was associated with increased type 1 diabetes risk. Five LA-related oxylipins, two ALA-related oxylipins and one DHA-related oxylipin were associated with decreased type 1 diabetes risk. A profile of elevated LA- and ALA-related oxylipins (PC1) was associated with decreased type 1 diabetes risk (OR 0.61; 95% CI 0.40, 0.94). A profile of elevated ARA-related oxylipins (PC2) was associated with increased diabetes risk (OR 1.53; 95% CI 1.03, 2.29). A critical timepoint analysis showed type 1 diabetes was associated with a high ARA-related oxylipin profile at post-autoantibody-seroconversion but not pre-seroconversion. CONCLUSIONS/

interpretationThe protective association of higher LA- and ALA-related oxylipins demonstrates the importance of both inflammation promotion and resolution in type 1 diabetes. Proinflammatory ARA-related oxylipins may play an important role once the autoimmune process has begun.

Indexed as

AdolescentArachidonic AcidAutoantibodiesAutoimmunityCase-Control StudiesChildChild, PreschoolChromatography, High Pressure LiquidDiabetes Mellitus, Type 1Docosahexaenoic AcidsFemaleFollow-Up StudiesGlutamate DecarboxylaseHLA-DR3 AntigenHLA-DR4 AntigenHumansArachidonic AcidAutoantibodiesDocosahexaenoic AcidsGlutamate DecarboxylaseHLA-DR3 AntigenHLA-DR4 AntigenInsulinLinoleic AcidOxylipinsPTPRN protein, humanReceptor-Like Protein Tyrosine Phosphatases, Class 8InflammationLipid mediatorsOxylipinsPaediatricProinflammatoryPro-resolvingType 1 diabetes

Identifiers

PMID33893822
PMCPMC8249332
OpenAlexW3156241850

What OpenQuestion holds

Textmetadata
LicenceTDM
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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.