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孕期母体血红蛋白水平与儿童 DNA 甲基化:孕期和儿童期表观遗传学联盟的一项研究。

Maternal haemoglobin levels in pregnancy and child DNA methylation: a study in the pregnancy and childhood epigenetics consortium.

机构信息

Center for Life Course Health Research, University of Oulu, Oulu, Finland.

Generation R Study Group, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.

出版信息

Epigenetics. 2022 Jan;17(1):19-31. doi: 10.1080/15592294.2020.1864171. Epub 2021 Jan 11.

DOI:10.1080/15592294.2020.1864171
PMID:33331245
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8813068/
Abstract

Altered maternal haemoglobin levels during pregnancy are associated with pre-clinical and clinical conditions affecting the fetus. Evidence from animal models suggests that these associations may be partially explained by differential DNA methylation in the newborn with possible long-term consequences. To test this in humans, we meta-analyzed the epigenome-wide associations of maternal haemoglobin levels during pregnancy with offspring DNA methylation in 3,967 newborn cord blood and 1,534 children and 1,962 adolescent whole-blood samples derived from 10 cohorts. DNA methylation was measured using Illumina Infinium Methylation 450K or MethylationEPIC arrays covering 450,000 and 850,000 methylation sites, respectively. There was no statistical support for the association of maternal haemoglobin levels with offspring DNA methylation either at individual methylation sites or clustered in regions. For most participants, maternal haemoglobin levels were within the normal range in the current study, whereas adverse perinatal outcomes often arise at the extremes. Thus, this study does not rule out the possibility that associations with offspring DNA methylation might be seen in studies with more extreme maternal haemoglobin levels.

摘要

怀孕期间母体血红蛋白水平的改变与影响胎儿的临床前和临床状况有关。动物模型的证据表明,这些关联可能部分可以通过新生儿中差异的 DNA 甲基化来解释,其可能具有长期后果。为了在人类中检验这一点,我们对 10 个队列中 3967 名新生儿脐带血和 1534 名儿童和 1962 名青少年全血样本中母体怀孕期间血红蛋白水平与后代 DNA 甲基化的全基因组关联进行了荟萃分析。使用 Illumina Infinium Methylation 450K 或 MethylationEPIC 阵列分别测量了 DNA 甲基化,这些阵列分别覆盖了 450000 和 850000 个甲基化位点。无论是在单个甲基化位点还是在区域中聚类,母体血红蛋白水平与后代 DNA 甲基化之间均没有统计学关联。对于大多数参与者,母体血红蛋白水平在当前研究中处于正常范围内,而不良围产期结局通常发生在极端情况下。因此,这项研究并不能排除在母体血红蛋白水平更极端的研究中可能会看到与后代 DNA 甲基化相关联的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de5a/8813068/d76512531d49/KEPI_A_1864171_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de5a/8813068/d76512531d49/KEPI_A_1864171_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de5a/8813068/d76512531d49/KEPI_A_1864171_F0001_OC.jpg

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