Cao-Lei Lei, Elgbeili Guillaume, Szyf Moshe, Laplante David P, King Suzanne
Department of Psychiatry, McGill University and Douglas Hospital Research Centre, Montreal, QC, Canada.
Douglas Hospital Research Centre, 6875 LaSalle Blvd, Montreal, QC, H4H 1R3, Canada.
BMC Res Notes. 2019 Mar 25;12(1):174. doi: 10.1186/s13104-019-4189-0.
Exposure to stress during pregnancy may program susceptibility to the development of obesity in offspring. Our goal was to determine whether prenatal maternal stress (PNMS) due to a natural disaster was associated with child obesity, and to compare the DNA methylation profiles in obese versus non-obese children at age 13½ years. Women and their children were involved in the longitudinal natural disaster study-Project Ice Strom, which served as a human model to study PNMS. Blood was collected from 31 children (including five obese children). Infinium HumanMethylation450 BeadChip Array was performed for genome-wide DNA methylation analyses.
Results demonstrated a well-defined obesity-associated genome-wide DNA methylation pattern. There were 277 CpGs, corresponding to 143 genes, were differentially-methylated. IPA analyses revealed 51 canonical pathways, and enrichment of pathways was involved in immune function. Although no significant association was found between PNMS and child obesity, the preliminary data in the study revealed obesity-associated methylation patterns on a genome-wide level in children.
孕期暴露于应激状态可能会使后代易于发生肥胖。我们的目标是确定自然灾害导致的产前母亲应激(PNMS)是否与儿童肥胖相关,并比较13.5岁肥胖儿童与非肥胖儿童的DNA甲基化谱。妇女及其子女参与了纵向自然灾害研究——冰暴项目,该项目作为研究PNMS的人类模型。从31名儿童(包括5名肥胖儿童)采集血液。采用Infinium HumanMethylation450 BeadChip芯片阵列进行全基因组DNA甲基化分析。
结果显示出明确的全基因组DNA甲基化模式,与肥胖相关。有277个CpG位点(对应143个基因)发生了差异甲基化。IPA分析揭示了51条经典通路,且这些通路的富集涉及免疫功能。虽然未发现PNMS与儿童肥胖之间存在显著关联,但该研究中的初步数据揭示了儿童全基因组水平上与肥胖相关的甲基化模式。