Division of Epidemiology, Biostatistics, and Environmental Health, School of Public Health, University of Memphis, Memphis, TN, USA.
School of Water, Energy and Environment, Cranfield University, Cranfield, MK43 0AL, Bedfordshire, UK.
Clin Epigenetics. 2021 Mar 25;13(1):64. doi: 10.1186/s13148-021-01042-4.
Previous studies have shown that DNA methylation (DNAm) is associated with body mass index (BMI). However, it is unknown whether DNAm at pre-adolescence is associated with BMI status transition from pre- to post-adolescence. In the Isle of Wight (IoW) birth cohort, genome-wide DNA methylation in whole blood was measured using Illumina Infinium Human450 and EPIC BeadChip arrays in n = 325 subjects, and pre- to post-adolescence BMI transition was classified into four groups: (1) normal to normal, (2) normal to overweight or obese, (3) overweight or obese to normal, and (4) persistent overweight or obese. We used recursive random forest to screen genome-wide Cytosine-phosphate-Guanine (CpG) sites with DNAm potentially associated with BMI transition for each gender, and the association of BMI status transition with DNAm at an earlier age was assessed via logistic regressions. To evaluate gender specificity, interactions between DNAm and gender were included in the model. Findings in the IoW cohort were further tested in an independent cohort, the Avon Longitudinal Study of Parents and Children (ALSPAC).
In total, 174 candidate CpGs were selected including CpGs from screening and CpGs previously associated correctionally with BMI in children and adults. Of these 174 CpGs, pre-adolescent DNAm of 38 CpGs in the IoW cohort was associated with BMI status transition, including 30 CpGs showing gender-specific associations. Thirteen CpGs showed consistent associations between the IoW cohort and the ALSPAC cohort (11 of which were gender-specific).
Pre-adolescence DNAm is associated with the change in BMI status from pre- to post-adolescence and such associations are likely to be gender-specific.
先前的研究表明,DNA 甲基化(DNAm)与体重指数(BMI)有关。然而,尚不清楚青春期前的 DNAm 是否与青春期前至青春期后的 BMI 状态变化有关。在怀特岛(IoW)出生队列中,使用 Illumina Infinium Human450 和 EPIC BeadChip 芯片在 n=325 名受试者中测量了全血的全基因组 DNA 甲基化,将 BMI 从青春期前到青春期后的变化分为四组:(1)正常到正常,(2)正常到超重或肥胖,(3)超重或肥胖到正常,(4)持续超重或肥胖。我们使用递归随机森林为每个性别筛选了可能与 BMI 变化相关的全基因组胞嘧啶磷酸鸟嘌呤(CpG)位点,并通过逻辑回归评估了更早年龄时的 BMI 状态变化与 DNAm 的关联。为了评估性别特异性,在模型中包含了 DNAm 与性别之间的相互作用。在怀特岛队列中发现的结果在一个独立的队列,即雅芳纵向父母和儿童研究(ALSPAC)中进行了进一步测试。
总共选择了 174 个候选 CpG,包括从筛选中获得的 CpG 和之前在儿童和成人中与 BMI 矫正相关的 CpG。在这 174 个 CpG 中,IoW 队列中 38 个 CpG 的青春期前 DNAm 与 BMI 状态变化有关,其中 30 个 CpG 表现出性别特异性关联。IoW 队列和 ALSPAC 队列之间有 13 个 CpG 表现出一致的关联(其中 11 个是性别特异性的)。
青春期前的 DNAm 与青春期前至青春期后的 BMI 状态变化有关,这种关联可能是性别特异性的。