Cadmium exposure and MEG3 methylation differences between Whites and African Americans in the NEST Cohort.

IF 4.8 Q1 GENETICS & HEREDITY
Environmental Epigenetics Pub Date : 2019-08-29 eCollection Date: 2019-07-01 DOI:10.1093/eep/dvz014
John S House, Jonathan Hall, Sarah S Park, Antonio Planchart, Eric Money, Rachel L Maguire, Zhiqing Huang, Carolyn J Mattingly, David Skaar, Jung Ying Tzeng, Thomas H Darrah, Avner Vengosh, Susan K Murphy, Randy L Jirtle, Cathrine Hoyo
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引用次数: 9

Abstract

Cadmium (Cd) is a ubiquitous environmental pollutant associated with a wide range of health outcomes including cancer. However, obscure exposure sources often hinder prevention efforts. Further, although epigenetic mechanisms are suspected to link these associations, gene sequence regions targeted by Cd are unclear. Aberrant methylation of a differentially methylated region (DMR) on the MEG3 gene that regulates the expression of a cluster of genes including MEG3, DLK1, MEG8, MEG9 and DIO3 has been associated with multiple cancers. In 287 infant-mother pairs, we used a combination of linear regression and the Getis-Ord Gi* statistic to determine if maternal blood Cd concentrations were associated with offspring CpG methylation of the sequence region regulating a cluster of imprinted genes including MEG3. Correlations were used to examine potential sources and routes. We observed a significant geographic co-clustering of elevated prenatal Cd levels and MEG3 DMR hypermethylation in cord blood (P = 0.01), and these findings were substantiated in our statistical models (β = 1.70, se = 0.80, P = 0.03). These associations were strongest in those born to African American women (β = 3.52, se = 1.32, P = 0.01) compared with those born to White women (β = 1.24, se = 2.11, P = 0.56) or Hispanic women (β = 1.18, se = 1.24, P = 0.34). Consistent with Cd bioaccumulation during the life course, blood Cd levels increased with age (β = 0.015 µg/dl/year, P = 0.003), and Cd concentrations were significantly correlated between blood and urine (ρ > 0.47, P < 0.01), but not hand wipe, soil or house dust concentrations (P > 0.05). Together, these data support that prenatal Cd exposure is associated with aberrant methylation of the imprint regulatory element for the MEG3 gene cluster at birth. However, neither house-dust nor water are likely exposure sources, and ingestion via contaminated hands is also unlikely to be a significant exposure route in this population. Larger studies are required to identify routes and sources of exposure.

Abstract Image

Abstract Image

Abstract Image

NEST队列中白人和非裔美国人的镉暴露和MEG3甲基化差异。
镉(Cd)是一种普遍存在的环境污染物,与包括癌症在内的多种健康结果有关。然而,不明的暴露来源往往阻碍预防工作。此外,尽管表观遗传学机制被怀疑与这些关联有关,但Cd靶向的基因序列区域尚不清楚。调节包括MEG3、DLK1、MEG8、MEG9和DIO3在内的一组基因表达的MEG3基因上差异甲基化区(DMR)的异常甲基化与多种癌症有关。在287对婴儿-母亲中,我们使用线性回归和Getis-Ord-Gi*统计的组合来确定母体血液Cd浓度是否与后代调节包括MEG3在内的一组印迹基因的序列区域的CpG甲基化有关。相关性被用来检查潜在的来源和途径。我们观察到脐血中产前Cd水平升高和MEG3 DMR高甲基化的显著地理共簇性(P = 0.01),这些发现在我们的统计模型中得到了证实(β = 1.70,se = 0.80,P = 0.03)。这些关联在非裔美国女性所生的孩子中最强(β = 3.52,se = 1.32,P = 0.01)与白人女性所生的相比(β = 1.24,se = 2.11,P = 0.56)或西班牙裔女性(β = 1.18,se = 1.24,P = 0.34)。与镉在生命过程中的生物累积一致,血液中的镉水平随着年龄的增长而增加(β = 0.015 µg/dl/年,P = 0.003),并且Cd浓度在血液和尿液之间显著相关(ρ > 0.47,P P > 0.05)。总之,这些数据支持产前镉暴露与出生时MEG3基因簇的印记调节元件的异常甲基化有关。然而,室内灰尘和水都不太可能是暴露源,通过受污染的手摄入也不太可能成为该人群的重要暴露途径。需要进行更大规模的研究,以确定暴露的途径和来源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Environmental Epigenetics
Environmental Epigenetics GENETICS & HEREDITY-
CiteScore
6.50
自引率
5.30%
发文量
0
审稿时长
17 weeks
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