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本文引用的文献

1
Reference-free deconvolution of DNA methylation data and mediation by cell composition effects.DNA甲基化数据的无参考去卷积及细胞组成效应介导
BMC Bioinformatics. 2016 Jun 29;17:259. doi: 10.1186/s12859-016-1140-4.
2
Differentially Methylated Genomic Regions in Birth-Weight Discordant Twin Pairs.出生体重不一致的双胞胎对中的差异甲基化基因组区域
Ann Hum Genet. 2016 Mar;80(2):81-7. doi: 10.1111/ahg.12146. Epub 2016 Feb 1.
3
Impact of Early Environment on Children's Mental Health: Lessons From DNA Methylation Studies With Monozygotic Twins.早期环境对儿童心理健康的影响:来自同卵双胞胎DNA甲基化研究的经验教训。
Twin Res Hum Genet. 2015 Dec;18(6):623-34. doi: 10.1017/thg.2015.84. Epub 2015 Nov 26.
4
Longitudinal analysis of DNA methylation associated with birth weight and gestational age.与出生体重和孕周相关的DNA甲基化的纵向分析
Hum Mol Genet. 2015 Jul 1;24(13):3752-63. doi: 10.1093/hmg/ddv119. Epub 2015 Apr 13.
5
Epigenetic signature of birth weight discordance in adult twins.成年双胞胎出生体重不一致的表观遗传特征。
BMC Genomics. 2014 Dec 4;15(1):1062. doi: 10.1186/1471-2164-15-1062.
6
Genome-wide DNA methylation variability in adolescent monozygotic twins followed since birth.自出生起随访的青少年同卵双胞胎的全基因组DNA甲基化变异性。
Epigenetics. 2014 Oct;9(10):1410-21. doi: 10.4161/15592294.2014.970060.
7
Delay of cortical thinning in very preterm born children.极早产儿皮质变薄延迟。
Early Hum Dev. 2014 Sep;90(9):443-50. doi: 10.1016/j.earlhumdev.2014.05.013. Epub 2014 Jun 27.
8
Grasping nettles: cellular heterogeneity and other confounders in epigenome-wide association studies.棘手问题:表观基因组关联研究中的细胞异质性及其他混杂因素
Hum Mol Genet. 2014 Sep 15;23(R1):R83-8. doi: 10.1093/hmg/ddu284. Epub 2014 Jun 13.
9
Prenatal origins of temperament: fetal growth, brain structure, and inhibitory control in adolescence.气质的产前起源:胎儿生长、脑结构与青少年期的抑制控制
PLoS One. 2014 May 6;9(5):e96715. doi: 10.1371/journal.pone.0096715. eCollection 2014.
10
Epigenetic variation in monozygotic twins: a genome-wide analysis of DNA methylation in buccal cells.同卵双胞胎的表观遗传变异:口腔细胞中 DNA 甲基化的全基因组分析。
Genes (Basel). 2014 May 5;5(2):347-65. doi: 10.3390/genes5020347.

青少年单卵双胞胎的出生体重不一致、DNA甲基化与皮质形态

Birth weight discordance, DNA methylation, and cortical morphology of adolescent monozygotic twins.

作者信息

Casey Kevin F, Levesque Melissa L, Szyf Moshe, Ismaylova Elmira, Verner Marie-Pier, Suderman Matthew, Vitaro Frank, Brendgen Mara, Dionne Ginette, Boivin Michel, Tremblay Richard E, Booij Linda

机构信息

CHU Sainte-Justine Research Center, Montreal, Québec, Canada.

Department of Psychiatry, University of Montreal, Montreal, Québec, Canada.

出版信息

Hum Brain Mapp. 2017 Apr;38(4):2037-2050. doi: 10.1002/hbm.23503. Epub 2016 Dec 29.

DOI:10.1002/hbm.23503
PMID:28032437
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6866862/
Abstract

BACKGROUND

Several studies have shown that the in utero environment, which can be indexed by birth weight (BW), is associated with cortical morphology in adolescence and adulthood. Work in monozygotic (MZ) twins suggests that this association is driven by non-shared environmental factors. This correlation could be the result of in utero impacts on DNA methylation. The aim of the present study with MZ twins is to replicate the association between discordance in BW and brain morphology and test whether discordance in DNA methylation mediates this relationship.

METHODS

One hundred and four adolescent MZ twins (52 pairs, of which 42% were male pairs) who have been followed regularly since birth underwent T1 weighted structural MRI, and epigenome-wide assessment of DNA methylation from saliva at age 15.

RESULTS

Co-twins had very similar measures of DNA methylation and cortical morphology. Higher BW members of a twin pair had increased total cortical surface area, and decreased cortical thickness compared to their lower BW sibling. BW Discordance was positively associated with both cortical surface area and cortical volume discordance. Genes involved in neurodevelopment were tentatively identified as mediators of both the BW - cortical volume, and BW- cortical surface area relationships.

CONCLUSIONS

The association between BW and cortical morphology in adolescence appears to be attributable to in utero environmental effects, and DNA methylation may play a role in mediating this relationship. Hum Brain Mapp 38:2037-2050, 2017. © 2017 Wiley Periodicals, Inc.

摘要

背景

多项研究表明,可通过出生体重(BW)来衡量的子宫内环境与青少年期及成年期的皮质形态有关。对同卵双胞胎(MZ)的研究表明,这种关联是由非共享环境因素驱动的。这种相关性可能是子宫内对DNA甲基化产生影响的结果。本研究以同卵双胞胎为对象,旨在重复出生体重差异与脑形态之间的关联,并测试DNA甲基化差异是否介导了这种关系。

方法

104名自出生后就接受定期随访的青少年同卵双胞胎(52对,其中42%为男性双胞胎对)接受了T1加权结构磁共振成像(MRI)检查,并在15岁时对唾液进行了全基因组DNA甲基化评估。

结果

双胞胎的DNA甲基化和皮质形态测量结果非常相似。与出生体重较低的同胞相比,双胞胎中出生体重较高的成员总皮质表面积增加,皮质厚度减小。出生体重差异与皮质表面积差异和皮质体积差异均呈正相关。初步确定参与神经发育的基因是出生体重与皮质体积、出生体重与皮质表面积关系的介导因素。

结论

青少年期出生体重与皮质形态之间的关联似乎归因于子宫内环境效应,DNA甲基化可能在介导这种关系中发挥作用。《人类大脑图谱》38:2037 - 2050,2017年。© 2017威利期刊公司。