An epigenome-wide association study of child appetitive traits and DNA methylation

被引:2
|
作者
Harris, Holly A. [1 ,2 ,3 ]
Friedman, Chloe [4 ,5 ]
Starling, Anne P. [4 ,5 ,6 ]
Dabelea, Dana [4 ,5 ,7 ]
Johnson, Susan L. [8 ]
Fuemmeler, Bernard F. [9 ]
Jima, Dereje [10 ,11 ]
Murphy, Susan K. [12 ]
Hoyo, Cathrine [13 ]
Jansen, Pauline W. [1 ,2 ,3 ]
Felix, Janine F. [2 ,14 ]
Mulder, Rosa H. [2 ,14 ]
机构
[1] Univ Med Ctr, Dept Child & Adolescent Psychiat Psychol, Erasmus MC, Rotterdam, Netherlands
[2] Univ Med Ctr Rotterdam, Erasmus MC, Generat R Study Grp, Rotterdam, Netherlands
[3] Erasmus Univ, Dept Psychol Educ & Child Studies, POB 1738, NL-3000 DR Rotterdam, Netherlands
[4] Univ Colorado, Colorado Sch Publ Hlth, Dept Epidemiol, Anschutz Med Campus, Aurora, CO USA
[5] Univ Colorado, Lifecourse Epidemiol Adipos & Diabet LEAD Ctr, Anschutz Med Campus, Aurora, CO USA
[6] Univ N Carolina, Gillings Sch Global Publ Hlth, Dept Epidemiol, Chapel Hill, NC USA
[7] Univ Colorado, Sch Med, Dept Pediat, Anschutz Med Campus, Aurora, CO USA
[8] Univ Colorado, Dept Pediat, Sch Med, Sect Nutr, Anschutz Med Campus, Aurora, CO USA
[9] Virginia Commonwealth Univ, Massey Comprehens Canc Ctr, Richmond, VA USA
[10] North Carolina State Univ, Bioinformat Res Ctr, Raleigh, NC USA
[11] North Carolina State Univ, Ctr Human Hlth & Environm, Raleigh, NC USA
[12] Duke Univ, Dept Obstet & Gynecol Reprod Sci, Med Ctr, Durham, NC USA
[13] North Carolina State Univ, Ctr Human Hlth & Environm, Dept Biol Sci, Raleigh, NC USA
[14] Univ Med Ctr Rotterdam, Dept Pediat, Erasmus MC, Rotterdam, Netherlands
基金
欧盟地平线“2020”;
关键词
Appetitive traits; Childhood; DNA methylation; Epigenome-wide association study; Epigenetics; Eating behaviors; GESTATIONAL WEIGHT-GAIN; BODY-MASS INDEX; FOOD FUSSINESS; MATERNAL BMI; OBESITY; PREGNANCY; BEHAVIOR; PATTERNS; BIRTH; IMPUTATION;
D O I
10.1016/j.appet.2023.107086
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
The etiology of childhood appetitive traits is poorly understood. Early-life epigenetic processes may be involved in the developmental programming of appetite regulation in childhood. One such process is DNA methylation (DNAm), whereby a methyl group is added to a specific part of DNA, where a cytosine base is next to a guanine base, a CpG site. We meta-analyzed epigenome-wide association studies (EWASs) of cord blood DNAm and early -childhood appetitive traits. Data were from two independent cohorts: the Generation R Study (n = 1,086, Rotterdam, the Netherlands) and the Healthy Start study (n = 236, Colorado, USA). DNAm at autosomal methylation sites in cord blood was measured using the Illumina Infinium HumanMethylation450 BeadChip. Parents reported on their child's food responsiveness, emotional undereating, satiety responsiveness and food fussiness using the Children's Eating Behaviour Questionnaire at age 4-5 years. Multiple regression models were used to examine the association of DNAm (predictor) at the individual site-and regional-level (using DMRff) with each appetitive trait (outcome), adjusting for covariates. Bonferroni-correction was applied to adjust for multiple testing. There were no associations of DNAm and any appetitive trait when examining individual CpG-sites. However, when examining multiple CpGs jointly in so-called differentially methylated regions, we identified 45 associations of DNAm with food responsiveness, 7 associations of DNAm with emotional undereating, 13 associations of DNAm with satiety responsiveness, and 9 associations of DNAm with food fussiness. This study shows that DNAm in the newborn may partially explain variation in appetitive traits expressed in early childhood and provides preliminary support for early programming of child appetitive traits through DNAm. Investigating differential DNAm associated with appetitive traits could be an important first step in identifying biological pathways underlying the development of these behaviors.
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页数:11
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