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Lower Placental Leptin Promoter Methylation in Association with Fine Particulate Matter Air Pollution during Pregnancy and Placental Nitrosative Stress at Birth in the ENVIRONAGE Cohort

机译:环境队列中较低的胎盘瘦素启动子甲基化与妊娠期间的细颗粒物空气污染以及出生时胎盘的亚硝化应激有关

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Background: Particulate matter with a diameter ≤ 2.5 μm (PM2.5) affects human fetal development during pregnancy. Oxidative stress is a putative mechanism by which PM2.5 may exert its effects. Leptin (LEP) is an energy-regulating hormone involved in fetal growth and development. Objectives: We investigated in placental tissue whether DNA methylation of the LEP promoter is associated with PM2.5 and whether the oxidativeitrosative stress biomarker 3-nitrotyrosine (3-NTp) is involved. Methods: LEP DNA methylation status of 361 placentas from the ENVIRONAGE birth cohort was assessed using bisulfite-PCR-pyrosequencing. Placental 3-NTp (n = 313) was determined with an ELISA assay. Daily PM2.5 exposure levels were estimated for each mother’s residence, accounting for residential mobility during pregnancy, using a spatiotemporal interpolation model. Results: After adjustment for a priori chosen covariates, placental LEP methylation was 1.4% lower (95% CI: –2.7, –0.19%) in association with an interquartile range increment (7.5 μg/m3) in second-trimester PM2.5 exposure and 0.43% lower (95% CI: –0.85, –0.02%) in association with a doubling of placental 3-NTp content. Conclusions: LEP methylation status in the placenta was negatively associated with PM2.5 exposure during the second trimester, and with placental 3-NTp, a marker of oxidativeitrosative stress. Additional research is needed to confirm our findings and to assess whether oxidativeitrosative stress might contribute to associations between PM2.5 and placental epigenetic events. Potential consequences for health during the neonatal period and later in life warrant further exploration. Citation: Saenen ND, Vrijens K, Janssen BG, Roels HA, Neven KY, Vanden Berghe W, Gyselaers W, Vanpoucke C, Lefebvre W, De Boever P, Nawrot TS. 2017. Lower placental leptin promoter methylation in association with fine particulate matter air pollution during pregnancy and placental nitrosative stress at birth in the ENVIRONAGE cohort. Environ Health Perspect 125:262–268;?http://dx.doi.org/10.1289/EHP38.
机译:背景:直径≤2.5μm(PM2.5)的颗粒物质会影响怀孕期间人类胎儿的发育。氧化应激是PM2.5发挥其作用的推测机制。瘦素(LEP)是一种参与胎儿生长发育的能量调节激素。目的:我们在胎盘组织中研究了LEP启动子的DNA甲基化是否与PM2.5相关以及是否存在氧化/亚硝化应激生物标记物3-硝基酪氨酸(3-NTp)。方法:使用亚硫酸氢盐-PCR-焦磷酸测序法评估了ENVIRONAGE出生人群中361个胎盘的LEP DNA甲基化状态。用ELISA测定法测定胎盘3-NTp(n = 313)。使用时空插值模型估算了每个母亲的住所每天的PM2.5暴露水平,并考虑了怀孕期间的住所流动性。结果:对先验选择的协变量进行校正后,孕中期PM2.5暴露导致胎盘LEP甲基化降低1.4%(95%CI:–2.7,–0.19%),四分位间距增加(7.5μg/ m3)胎盘3-NTp含量翻倍,则降低了0.43%(95%CI:-0.85,-0.02%)。结论:胎盘中LEP甲基化状态与妊娠中期PM2.5暴露负相关,与胎盘3-NTp(氧化/亚硝基应激的标志物)负相关。需要进一步的研究来证实我们的发现,并评估氧化/亚硝基应激是否可能有助于PM2.5与胎盘表观遗传事件之间的关联。新生儿期和生命后期对健康的潜在后果值得进一步探索。引用:Saenen ND,Vrijens K,Janssen BG,Roels HA,Neven KY,Vanden Berghe W,Gyselaers W,Vanpoucke C,Lefebvre W,De Boever P,Nawrot TS。 2017年。ENVIRONAGE队列中胎盘瘦素启动子甲基化水平降低与怀孕期间的细颗粒物空气污染以及出生时胎盘的亚硝化应激有关。 Environ Health Perspect 125:262–268; http://dx.doi.org/10.1289/EHP38。

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