Differentially methylated regions interrogated for metastable epialleles associate with offspring adiposity

被引:0
|
作者
Waldrop, Stephanie W. [1 ]
Sauder, Katherine A. [1 ,2 ]
Niemiec, Sierra S. [3 ]
Kechris, Katerina J. [3 ]
Yang, Ivana, V [4 ]
Starling, Anne P. [2 ,5 ]
Perng, Wei [2 ]
Dabelea, Dana [2 ]
Borengasser, Sarah J. [1 ]
机构
[1] Univ Colorado Anschutz Med Campus, Dept Pediat, Sect Nutr, Aurora, CO 80045 USA
[2] Univ Colorado Anschutz Med Campus, Lifecourse Epidemiol Adipos & Diabet LEAD Ctr, Aurora, CO 80045 USA
[3] Univ Colorado Anschutz Med Campus, Ctr Innovat Design & Anal, Aurora, CO 80045 USA
[4] Univ Colorado Anschutz Med Campus, Dept Biomed Informat, Aurora, CO 80045 USA
[5] Univ North Carolina Chapel Hill, Dept Epidemiol, Chapel Hill, NC 27599 USA
基金
美国国家卫生研究院;
关键词
adiposity; biomarkers; childhood obesity; DNA methylation; metastable epialleles; BODY-COMPOSITION ASSESSMENT; BLOOD DNA METHYLATION; RAPID WEIGHT-GAIN; SUBSET-QUANTILE; CHILDHOOD; OBESITY; INFANCY; BIRTH; NORMALIZATION; TRAJECTORIES;
D O I
10.1080/17501911.2024.2359365
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Aim: Assess if cord blood differentially methylated regions (DMRs) representing human metastable epialleles (MEs) associate with offspring adiposity in 588 maternal-infant dyads from the Colorado Health Start Study. Materials & methods: DNA methylation was assessed via the Illumina 450K array (similar to 439,500 CpG sites). Offspring adiposity was obtained via air displacement plethysmography. Linear regression modeled the association of DMRs potentially representing MEs with adiposity. Results & conclusion: We identified two potential MEs, ZFP57, which associated with infant adiposity change and B4GALNT4, which associated with infancy and childhood adiposity change. Nine DMRs annotating to genes that annotated to MEs associated with change in offspring adiposity (false discovery rate <0.05). Methylation of approximately 80% of DMRs identified associated with decreased change in adiposity.
引用
收藏
页码:1215 / 1230
页数:16
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