Suppr超能文献

密歇根州孕期队列中母体线粒体DNA拷贝数和甲基化作为妊娠结局潜在预测指标的研究

Maternal mitochondrial DNA copy number and methylation as possible predictors of pregnancy outcomes in a Michigan pregnancy cohort.

作者信息

Cinzori Maria E, Nicol Megan, Dewald Alisa L, Goodrich Jaclyn M, Zhou Zheng, Gardiner Joseph C, Kerver Jean M, Dolinoy Dana C, Talge Nicole, Strakovsky Rita S

机构信息

Department of Food Science and Human Nutrition, Michigan State University, East Lansing, MI 48824, United States.

Institute for Integrative Toxicology, Michigan State University, East Lansing, MI 48824, United States.

出版信息

Environ Epigenet. 2024 Oct 29;10(1):dvae021. doi: 10.1093/eep/dvae021. eCollection 2024.

Abstract

Little is understood about the roles of mitochondria in pregnancy-related adaptations. Therefore, we evaluated associations of maternal early-to-mid pregnancy mitochondrial DNA copy number (mtDNAcn) and mtDNA methylation with birth size and gestational length. Michigan women ( = 396) provided venous bloodspots at median 11 weeks gestation to quantify mtDNAcn marker NADH-ubiquinone oxidoreductase chain 1 () using real-time quantitative PCR and mtDNA methylation at several regions within four mitochondria-specific genes using pyrosequencing: (mitochondrially encoded tRNA phenylalanine), (D-loop promoter region, heavy strand), (cytochrome b), and (D-loop promoter region, light strand). We abstracted gestational length and birthweight from birth certificates and calculated birthweight -scores using published references. We used multivariable linear regression to evaluate associations of mtDNAcn and mtDNA methylation with birthweight and birthweight -scores. Cox Proportional Hazards Models (PHMs) and quantile regression characterized associations of mitochondrial measures with gestational length. We also considered differences by fetal sex. Using linear regression and Cox PHMs, mtDNAcn was not associated with birth outcomes, whereas associations of mtDNA methylation with birth outcomes were inconsistent. However, using quantile regression, mtDNAcn was associated with shorter gestation in female newborns at the upper quantiles of gestational length, but with longer gestational length in males at the lower quantiles of gestational length. Maternal , and methylation was associated with longer gestational length in females at the upper quantiles and in males at lower gestational length quantiles. Maternal mtDNAcn and mtDNA methylation were associated with gestational length in babies born comparatively early or late, which could reflect adaptations in mitochondrial processes that regulate the length of gestation.

摘要

关于线粒体在妊娠相关适应性变化中的作用,我们了解得还很少。因此,我们评估了孕早期至孕中期母体线粒体DNA拷贝数(mtDNAcn)和mtDNA甲基化与出生体重及妊娠时长之间的关联。密歇根州的396名女性在妊娠11周时提供了静脉血斑,通过实时定量PCR对mtDNAcn标记物烟酰胺腺嘌呤二核苷酸泛醌氧化还原酶链1()进行定量,并使用焦磷酸测序法对四个线粒体特异性基因内几个区域的mtDNA甲基化进行检测:(线粒体编码的苯丙氨酸tRNA)、(D环启动子区域,重链)、(细胞色素b)和(D环启动子区域,轻链)。我们从出生证明中提取了妊娠时长和出生体重,并使用已发表的参考文献计算出生体重评分。我们使用多变量线性回归来评估mtDNAcn和mtDNA甲基化与出生体重及出生体重评分之间的关联。Cox比例风险模型(PHMs)和分位数回归分析了线粒体指标与妊娠时长之间的关联。我们还考虑了胎儿性别的差异。通过线性回归和Cox PHMs分析,mtDNAcn与出生结局无关,而mtDNA甲基化与出生结局的关联并不一致。然而,使用分位数回归分析发现,在妊娠时长较高分位数的女性新生儿中,mtDNAcn与较短的妊娠时长相关,而在妊娠时长较低分位数的男性中,mtDNAcn与较长的妊娠时长相关。母体、和甲基化与较高分位数的女性及较低妊娠时长分位数的男性的较长妊娠时长相关。母体mtDNAcn和mtDNA甲基化与相对早产或晚产婴儿的妊娠时长相关,这可能反映了线粒体过程中调节妊娠时长的适应性变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2497/11614404/e3cf0e4bdbfe/dvae021f1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验