An Oxylipin-Related Nutrient Pattern and Risk of Type 1 Diabetes in the Diabetes Autoimmunity Study in the Young (DAISY)

Author:

Buckner Teresa12,Johnson Randi K.13ORCID,Vanderlinden Lauren A.1,Carry Patrick M.14,Romero Alex3,Onengut-Gumuscu Suna5,Chen Wei-Min5,Fiehn Oliver6ORCID,Frohnert Brigitte I.1,Crume Tessa1,Perng Wei1ORCID,Kechris Katerina1ORCID,Rewers Marian1,Norris Jill M.1ORCID

Affiliation:

1. Department of Epidemiology, Colorado School of Public Health, CU Anschutz, Anschutz Medical Campus, Aurora, CO 80045, USA

2. Department of Kinesiology, Nutrition, and Dietetics, University of Northern Colorado, Greeley, CO 80639, USA

3. Department of Biomedical Informatics, CU School of Medicine, Anschutz Medical Campus, Aurora, CO 80045, USA

4. Colorado Program for Musculoskeletal Research, Department of Orthopedics, CU School of Medicine, Anschutz Medical Campus, Aurora, CO 80045, USA

5. Health Center for Public Health Genomics, University of Virginia, Charlottesville, VA 22903, USA

6. NIH-West Coast Metabolomics Center, University of California-Davis, Davis, CA 95616, USA

Abstract

Oxylipins, pro-inflammatory and pro-resolving lipid mediators, are associated with the risk of type 1 diabetes (T1D) and may be influenced by diet. This study aimed to develop a nutrient pattern related to oxylipin profiles and test their associations with the risk of T1D among youth. The nutrient patterns were developed with a reduced rank regression in a nested case-control study (n = 335) within the Diabetes Autoimmunity Study in the Young (DAISY), a longitudinal cohort of children at risk of T1D. The oxylipin profiles (adjusted for genetic predictors) were the response variables. The nutrient patterns were tested in the case-control study (n = 69 T1D cases, 69 controls), then validated in the DAISY cohort using a joint Cox proportional hazards model (n = 1933, including 81 T1D cases). The first nutrient pattern (NP1) was characterized by low beta cryptoxanthin, flavanone, vitamin C, total sugars and iron, and high lycopene, anthocyanidins, linoleic acid and sodium. After adjusting for T1D family history, the HLA genotype, sex and race/ethnicity, NP1 was associated with a lower risk of T1D in the nested case-control study (OR: 0.44, p = 0.0126). NP1 was not associated with the risk of T1D (HR: 0.54, p-value = 0.1829) in the full DAISY cohort. Future studies are needed to confirm the nested case-control findings and investigate the modifiable factors for oxylipins.

Funder

National Institutes of Health

NIH/NCATS Colorado CTSA

University of Colorado Diabetes Research Center

Colorado Clinical and Translational Sciences Institute

American Diabetes Association

Publisher

MDPI AG

Subject

Food Science,Nutrition and Dietetics

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