Human Development and Health, Faculty of Medicine, University Hospital Southampton, University of Southampton, Duthie Building, MP808, Tremona Road, Southampton, Hampshire, SO16 6YD, UK.
Department of Community Medicine and Behavioral Sciences, Faculty of Medicine, Kuwait University, Kuwait City, Kuwait.
Clin Epigenetics. 2019 Aug 29;11(1):128. doi: 10.1186/s13148-019-0727-9.
Breastfeeding is protective against many long-term diseases, yet the mechanisms involved are unknown. Leptin gene (LEP) is reported to be associated with body mass index (BMI). On the other hand, breastfeeding duration has been found to be associated with DNA methylation (DNAm) of the LEP gene. Therefore, epigenetic regulation of LEP may represent the mechanism underlying the protective effect of breastfeeding duration against obesity.
In the Isle of Wight Birth Cohort, peripheral blood DNAm at 23 cytosine-phosphate-guanine sites (CpGs) in the LEP locus in 10-year-old (n = 297) samples and 16 CpGs in 18-year-old (n = 305) samples, were generated using the Illumina Infinium MethylationEPIC and HumanMethylation450 Beadchips respectively and tested for association with breastfeeding duration (total and exclusive) using linear regression. To explore the association between breastfeeding durations and genome-wide DNAm, epigenome-wide association studies (EWASs) and differential methylation region (DMR) analyses were performed. BMI trajectories spanning the first 18 years of life were used as the outcome to test the association with breastfeeding duration (exposure) using multi-nominal logistic regression. Mediation analysis was performed for significant CpG sites.
Both total and exclusive breastfeeding duration were associated with DNAm at four LEP CpG sites at 10 years (P value < 0.05), and not at 18 years. Though no association was observed between breastfeeding duration and genome-wide DNAm, DMR analyses identified five significant differentially methylated regions (Sidak adjusted P value < 0.05). Breastfeeding duration was also associated with the early transient overweight trajectory. Furthermore, DNAm of LEP was associated with this trajectory at one CpG site and early persistent obesity at another, though mediation analysis was not significant.
Breastfeeding duration is associated with LEP methylation at age 10 years and BMI trajectory. LEP DNAm is also significantly associated with BMI trajectories throughout childhood, though sample sizes were small. However, mediation analysis did not demonstrate that DNAm of LEP explained the protective effect of breastfeeding against childhood obesity.
母乳喂养对许多长期疾病具有保护作用,但其中涉及的机制尚不清楚。瘦素基因(LEP)据报道与体重指数(BMI)有关。另一方面,母乳喂养的持续时间与 LEP 基因的 DNA 甲基化(DNAm)有关。因此,LEP 的表观遗传调控可能代表了母乳喂养持续时间对肥胖的保护作用的机制。
在怀特岛出生队列中,使用 Illumina Infinium MethylationEPIC 和 HumanMethylation450 Beadchips 在 10 岁(n=297)和 18 岁(n=305)样本中生成了 LEP 基因座上 23 个胞嘧啶磷酸鸟嘌呤位点(CpG)的外周血 DNAm,测试了与母乳喂养持续时间(总时间和纯母乳喂养时间)的关联,采用线性回归。为了探索母乳喂养持续时间与全基因组 DNAm 的关联,进行了全基因组关联研究(EWAS)和差异甲基化区域(DMR)分析。使用 18 岁前的 BMI 轨迹作为结果,使用多分类逻辑回归测试与母乳喂养持续时间(暴露)的关联。对显著的 CpG 位点进行中介分析。
总母乳喂养时间和纯母乳喂养时间都与 10 岁时 LEP 的四个 CpG 位点的 DNAm 相关(P 值<0.05),而在 18 岁时则没有。虽然没有观察到母乳喂养持续时间与全基因组 DNAm 之间的关联,但 DMR 分析确定了五个显著的差异甲基化区域(Sidak 调整后的 P 值<0.05)。母乳喂养持续时间也与早期过渡性超重轨迹相关。此外,LEP 的 DNAm 在一个 CpG 位点与该轨迹相关,在另一个 CpG 位点与早期持续肥胖相关,尽管中介分析没有统计学意义。
母乳喂养持续时间与 10 岁时的 LEP 甲基化和 BMI 轨迹相关。LEP 的 DNAm 也与儿童期整个 BMI 轨迹显著相关,尽管样本量较小。然而,中介分析并未表明 LEP 的 DNAm 解释了母乳喂养对儿童肥胖的保护作用。