Longitudinal DNA methylation differences precede type 1 diabetes

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作者
Randi K. Johnson
Lauren A. Vanderlinden
Fran Dong
Patrick M. Carry
Jennifer Seifert
Kathleen Waugh
Hanan Shorrosh
Tasha Fingerlin
Brigitte I. Frohnert
Ivana V. Yang
Katerina Kechris
Marian Rewers
Jill M. Norris
机构
[1] University of Colorado Anschutz Medical Campus,Barbara Davis Center for Diabetes
[2] Division of Biomedical Informatics and Personalized Medicine,undefined
[3] Colorado School of Public Health,undefined
[4] Department of Biostatistics and Informatics,undefined
[5] University of Colorado Anschutz Medical Campus,undefined
[6] Colorado School of Public Health,undefined
[7] Department of Epidemiology,undefined
[8] National Jewish Health,undefined
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摘要
DNA methylation may be involved in development of type 1 diabetes (T1D), but previous epigenome-wide association studies were conducted among cases with clinically diagnosed diabetes. Using multiple pre-disease peripheral blood samples on the Illumina 450 K and EPIC platforms, we investigated longitudinal methylation differences between 87 T1D cases and 87 controls from the prospective Diabetes Autoimmunity Study in the Young (DAISY) cohort. Change in methylation with age differed between cases and controls in 10 regions. Average longitudinal methylation differed between cases and controls at two genomic positions and 28 regions. Some methylation differences were detectable and consistent as early as birth, including before and after the onset of preclinical islet autoimmunity. Results map to transcription factors, other protein coding genes, and non-coding regions of the genome with regulatory potential. The identification of methylation differences that predate islet autoimmunity and clinical diagnosis may suggest a role for epigenetics in T1D pathogenesis; however, functional validation is warranted.
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