Joubert Bonnie R, Håberg Siri E, Bell Douglas A, Nilsen Roy M, Vollset Stein Emil, Midttun Oivind, Ueland Per Magne, Wu Michael C, Nystad Wenche, Peddada Shyamal D, London Stephanie J
Authors' Affiliations: Division of Intramural Research, National Institute of Environmental Health Sciences (NIEHS), National Institutes of Health, Department of Health and Human Services, Research Triangle Park, North Carolina; Fred Hutchinson Cancer Research Center, Seattle, Washington; Norwegian Institute of Public Health, Oslo; Haukeland University Hospital; University of Bergen; and Bevital A/S, Laboratoriebygget, Bergen, Norway.
Authors' Affiliations: Division of Intramural Research, National Institute of Environmental Health Sciences (NIEHS), National Institutes of Health, Department of Health and Human Services, Research Triangle Park, North Carolina; Fred Hutchinson Cancer Research Center, Seattle, Washington; Norwegian Institute of Public Health, Oslo; Haukeland University Hospital; University of Bergen; and Bevital A/S, Laboratoriebygget, Bergen, NorwayAuthors' Affiliations: Division of Intramural Research, National Institute of Environmental Health Sciences (NIEHS), National Institutes of Health, Department of Health and Human Services, Research Triangle Park, North Carolina; Fred Hutchinson Cancer Research Center, Seattle, Washington; Norwegian Institute of Public Health, Oslo; Haukeland University Hospital; University of Bergen; and Bevital A/S, Laboratoriebygget, Bergen, Norway.
Cancer Epidemiol Biomarkers Prev. 2014 Jun;23(6):1007-17. doi: 10.1158/1055-9965.EPI-13-1256. Epub 2014 Apr 16.
Maternal smoking in pregnancy is associated with adverse health outcomes in children, including cancers; underlying mechanisms may include epigenetic modifications. Using Illumina's 450K array, we previously identified differential DNA methylation related to maternal smoking during pregnancy at 26 CpG sites (CpGs) in 10 genes in newborn cord bloods from the Norwegian Mother and Child Cohort Study (MoBa). Whether these methylation signals in newborns reflect in utero exposure only or possibly epigenetic inheritance of smoking-related modifications is unclear.
We therefore evaluated the impact of the timing of mother's smoking (before or during pregnancy using cotinine measured at 18 weeks gestation), the father's smoking before conception, and the grandmother's smoking during her pregnancy with the mother on methylation at these 26 CpGs in 1,042 MoBa newborns. We used robust linear regression, adjusting for covariates, applying Bonferroni correction.
The strongest and only statistically significant associations were observed for sustained smoking by the mother during pregnancy through at least gestational week 18 (P < 1.6 × 10(-5) for all 26 CpGs). We observed no statistically significant differential methylation due to smoking by the mother before pregnancy or that ceased by week 18, father's smoking before conception, or grandmother's smoking while pregnant with the mother.
Differential methylation at these CpGs in newborns seems to reflect sustained in utero exposure rather than epigenetic inheritance.
Smoking cessation in early pregnancy may negate effects on methylation. Analyses of maternal smoking during pregnancy and offspring health outcomes, including cancer, limited to ever smoking might miss true associations. Cancer Epidemiol Biomarkers Prev; 23(6); 1007-17. ©2014 AACR.
孕期母亲吸烟与儿童的不良健康结局相关,包括癌症;潜在机制可能包括表观遗传修饰。利用Illumina公司的450K芯片,我们之前在挪威母婴队列研究(MoBa)的新生儿脐带血中,于10个基因的26个CpG位点(CpGs)鉴定出与孕期母亲吸烟相关的DNA甲基化差异。目前尚不清楚新生儿中的这些甲基化信号是仅反映子宫内暴露,还是可能反映吸烟相关修饰的表观遗传遗传。
因此,我们评估了母亲吸烟时间(孕期前或孕期,使用妊娠18周时测量的可替宁)、父亲受孕前吸烟以及祖母孕期吸烟对1042名MoBa新生儿中这26个CpG位点甲基化的影响。我们使用稳健线性回归,对协变量进行调整,并应用Bonferroni校正。
在孕期至少持续吸烟至妊娠第18周的母亲中,观察到最强且唯一具有统计学意义的关联(所有26个CpG位点的P<1.6×10-5)。我们未观察到因母亲孕期前吸烟或在第18周前戒烟、父亲受孕前吸烟或祖母孕期吸烟导致的具有统计学意义的甲基化差异。
新生儿中这些CpG位点的甲基化差异似乎反映了持续的子宫内暴露,而非表观遗传遗传。
孕早期戒烟可能消除对甲基化的影响。对孕期母亲吸烟与包括癌症在内的后代健康结局的分析,若仅限于曾经吸烟,可能会遗漏真正的关联。《癌症流行病学、生物标志物与预防》;23(6);1007 - 17。©2014美国癌症研究协会。