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本文引用的文献

1
Prenatal gestational diabetes mellitus exposure and accelerated offspring DNA methylation age in early childhood.产前妊娠糖尿病暴露与儿童早期后代 DNA 甲基化年龄加速。
Epigenetics. 2021 Jan-Feb;16(2):186-195. doi: 10.1080/15592294.2020.1790924. Epub 2020 Jul 11.
2
Maternal MTNR1B genotype, maternal gestational weight gain, and childhood obesity.母亲 MTNR1B 基因型、孕期体重增加与儿童肥胖。
Am J Clin Nutr. 2020 Feb 1;111(2):360-368. doi: 10.1093/ajcn/nqz296.
3
Maternal Gestational Diabetes Mellitus and Newborn DNA Methylation: Findings From the Pregnancy and Childhood Epigenetics Consortium.孕妇妊娠期糖尿病与新生儿DNA甲基化:来自妊娠与儿童表观遗传学联盟的研究结果。
Diabetes Care. 2020 Jan;43(1):98-105. doi: 10.2337/dc19-0524. Epub 2019 Oct 10.
4
In-depth characterization of the placental imprintome reveals novel differentially methylated regions across birth weight categories.深入分析胎盘印迹组学揭示了不同出生体重类别中新的差异甲基化区域。
Epigenetics. 2020 Jan-Feb;15(1-2):47-60. doi: 10.1080/15592294.2019.1647945. Epub 2019 Aug 12.
5
Epigenetic alteration of Rho guanine nucleotide exchange Factor 11 (ARHGEF11) in cord blood samples in macrosomia exposed to intrauterine hyperglycemia.宫内高血糖暴露的巨大儿脐带血样本中 Rho 鸟嘌呤核苷酸交换因子 11(ARHGEF11)的表观遗传改变。
J Matern Fetal Neonatal Med. 2021 Feb;34(3):422-431. doi: 10.1080/14767058.2019.1609929. Epub 2019 Apr 30.
6
Maternal gestational diabetes and different indicators of childhood obesity: a large study.母亲妊娠期糖尿病与儿童肥胖的不同指标:一项大型研究。
Endocr Connect. 2018 Dec;7(12):1464-1471. doi: 10.1530/EC-18-0449.
7
Foetal Macrosomia and Foetal-Maternal Outcomes at Birth.出生时的胎儿巨大及胎儿-母亲结局
J Pregnancy. 2018 Aug 8;2018:4790136. doi: 10.1155/2018/4790136. eCollection 2018.
8
DNA methylation of imprinted genes at birth is associated with child weight status at birth, 1 year, and 3 years.出生时印迹基因的 DNA 甲基化与出生时、1 岁和 3 岁时儿童的体重状况有关。
Clin Epigenetics. 2018 Jun 28;10:90. doi: 10.1186/s13148-018-0521-0. eCollection 2018.
9
Birth weight predicts aging trajectory: A hypothesis.出生体重预测衰老轨迹:一种假说。
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Natl Vital Stat Rep. 2017 Jan;66(1):1.

妊娠糖尿病与巨大儿之间新的表观遗传学联系。

Novel epigenetic link between gestational diabetes mellitus and macrosomia.

机构信息

Center for Global Oncology, Institute for Global Health, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.

Tianjin Women's & Children's Health Center, Tianjin, China.

出版信息

Epigenomics. 2021 Aug;13(15):1221-1230. doi: 10.2217/epi-2021-0096. Epub 2021 Aug 2.

DOI:10.2217/epi-2021-0096
PMID:34337972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8371577/
Abstract

Examine maternal gestational diabetes mellitus (GDM), macrosomia and DNA methylation in candidate genes , , , , , ,  and . A total of 1145 children (572 GDM cases and 573 controls) from the Tianjin GDM study, including 177 with macrosomia, had blood DNA collection at median age 5.9 (range: 3.1-10.0). We used logistic regression to screen for associations with GDM and model macrosomia on 37 CpGs, and performed mediation analysis. One CpG was associated with macrosomia at false discovery rate (FDR) <0.05 (cg14428359 in ); two (cg19466922 in and cg26263166 in ) were associated at p < 0.05 but mediated 26 and 13%, respectively. and were previously identified for potential involvement in fetal growth and development (Trial Registration number: NCT01554358 [ClinicalTrials.gov]).

摘要

检查母体妊娠糖尿病(GDM)、巨大儿和候选基因 、 、 、 、 、 的 DNA 甲基化。共有 1145 名儿童(572 例 GDM 病例和 573 例对照)来自天津 GDM 研究,其中 177 例为巨大儿,在中位数年龄 5.9 岁(范围:3.1-10.0)时采集血 DNA。我们使用逻辑回归筛选与 GDM 的关联,并对 37 个 CpG 进行模型分析,进行中介分析。一个 CpG 在 FDR <0.05 时与巨大儿相关( 中的 cg14428359); 两个 CpG 在 p<0.05 时与巨大儿相关,但分别介导了 26%和 13%( 和 中的 cg19466922 和 cg26263166)。 、 、 、 、 、 和 先前被鉴定为可能参与胎儿生长发育(试验注册号:NCT01554358 [ClinicalTrials.gov])。