Evidence map›Paper›PMID 41162339›Full record

ArticleThe Journal of clinical endocrinology and metabolism2026

Increased Levels of the Vitamin D Metabolite Ratio Are Protective Against Progression From Islet Autoimmunity to T1D.

Patrick M Carry, Soojeong Kim, Nicole L Zwick, Teresa Buckner, Brian DeFelice, Randi K Johnson, Jennifer Seifert, Kathleen Waugh, Fran Dong, Lauren A Vanderlinden and 5 more

Abstract read
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Patrick M CarryDepartment of Orthopedics, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.ORCID 0000-0002-2989-7080
Soojeong KimDepartment of Epidemiology, Colorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.ORCID 0000-0002-2453-5945
Nicole L ZwickDepartment of Epidemiology, Colorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.ORCID 0009-0007-5183-918X
Teresa BucknerDepartment of Epidemiology, Colorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.ORCID 0000-0002-5831-1683
Brian DeFeliceChan Zuckerberg Biohub, San Francisco, CA 94158, USA.ORCID 0000-0001-8243-0300
Randi K JohnsonDepartment of Epidemiology, Colorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.ORCID 0000-0001-9345-4439
Jennifer SeifertBarbara Davis Center, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.ORCID 0000-0001-5851-7246
Kathleen WaughBarbara Davis Center, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Fran DongBarbara Davis Center, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.ORCID 0009-0009-1456-8776
Lauren A VanderlindenDepartment of Biomedical Informatics, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.ORCID 0000-0002-4019-8395
Brigitte I FrohnertBarbara Davis Center, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.ORCID 0000-0002-6636-4048
Katerina KechrisDepartment of Biomedical Informatics, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.ORCID 0000-0002-3725-5459
Oliver FiehnWest Coast Metabolomics Center, University of California Davis, Davis, CA 95616, USA.ORCID 0000-0002-6261-8928
Marian RewersBarbara Davis Center, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.ORCID 0000-0003-3829-9207
Jill M NorrisDepartment of Epidemiology, Colorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.ORCID 0000-0001-8674-2598

Funding

Computational Bioscience Program Training GrantT15LM009451 · NLM · UNIVERSITY OF COLORADO DENVER · PI Katherina Kechris-Mays, Arjun Krishnan · 2007 to 2026
$11.7M
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
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
Islet Autoimmunity Reversion as a Model of T1D ResiliencyR21AI142483 · NIAID · UNIVERSITY OF COLORADO DENVER · PI NORRIS, JILL M · 2019 to 2020
$428k
NIAID NIH HHS R21 AI142483NIDDK NIH HHS P30 DK116073NIDDK NIH HHS R01 DK032493NIDDK NIH HHS R01 DK104351NIH HHS P30-DK116073NIH HHS R01-DK104351NIH HHS R01-DK32493NIH HHS R21-AI142483NLM NIH HHS T15 LM009451
6 · The paper itself

Abstract

contextIncreased levels of 25-hydroxyvitamin D (25OHD) have been protective against islet autoimmunity (IA), a preclinical type 1 diabetes (T1D) disease state. However, the role of 25OHD and downstream metabolites in progression from IA to T1D is not well understood.

objectiveWe hypothesized that downstream vitamin D metabolites and metabolite ratios would be associated with progression from IA to T1D.

methodsAmong participants at high genetic risk for T1D who developed IA (n = 143) in the Diabetes Autoimmunity Study in the Young (DAISY), a T1D birth cohort study, we quantified vitamin D3, 25OHD2, 3-epi-25OHD3, 25OHD3, 24,25(OH)2D3, and 1α,25(OH)2D3 metabolites from plasma samples using LC-MS/MS. We calculated the vitamin D metabolite ratio (VMR) (ie, 24,25(OH)2D3/25OHD3) and the epimer ratio (3-epi-25OHD3/25OHD3). We also tested the correlation between metabolite levels and gene expression in a subset of participants (n = 53).

resultsA total of 57/143 progressed to T1D. Higher VMR (hazard ratio (HR) per 1 SD increase: 0.65; 95% CI: 0.49-0.88) and levels of 24,25(OH)2D3 (HR per 1 SD increase: 0.72; 95% CI: 0.55-0.94) at IA seroconversion were associated with a lower risk of progression to T1D, adjusting for seroconversion age, season, HLA-DR3/4 genotype, and ancestry. Functional enrichment analysis suggests higher VMR resulted in a gene expression pattern in whole blood characteristic of decreased activation of inflammatory pathways related to neutrophil infiltration.

conclusionA higher VMR, a more functional measure of vitamin D status, was protective against T1D progression, perhaps by decreasing activation of inflammatory pathways.

Indexed as

AutoimmunityDiabetes Mellitus, Type 1Islets of LangerhansVitamin DAdolescentAdultChildChild, PreschoolCohort StudiesDisease ProgressionFemaleHumansMaleYoung Adult25-hydroxyvitamin DVitamin DDAISYprogressiontype 1 diabetesvitamin Dvitamin D metabolite ratioVMR

Identifiers

PMID41162339
PMCPMC13099223

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.