DNA Methylation: An Epigenetic Risk Factor in Preterm Birth

被引:46
作者
Menon, Ramkumar [1 ]
Conneely, Karen N. [2 ]
Smith, Alicia K. [3 ]
机构
[1] Univ Texas Med Branch Galveston, Div Maternal Fetal Med, Dept Obstet & Gynecol, Galveston, TX 77555 USA
[2] Emory Univ, Sch Med, Dept Human Genet, Atlanta, GA USA
[3] Emory Univ, Sch Med, Dept Psychiat & Behav Sci, Atlanta, GA USA
关键词
prematurity; preterm labor; epigenetics; genetics; DNA; EARLY NUTRITION; FETAL-GROWTH; GENE; EXPOSURE; ENVIRONMENT; EXPRESSION; ORIGINS; BLOOD; CELLS; AGE;
D O I
10.1177/1933719111424446
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Spontaneous preterm birth (PTB; birth prior to 37 weeks of gestation) is a complex phenotype with multiple risk factors that complicate our understanding of its etiology. A number of recent studies have supported the hypothesis that epigenetic modifications such as DNA methylation induced by pregnancy-related risk factors may influence the risk of PTB or result in changes that predispose a neonate to adult-onset diseases. The critical role of timing of gene expression in the etiology of PTB makes it a highly relevant disorder in which to examine the potential role of epigenetic changes. Because changes in DNA methylation patterns can result in long-term consequences, it is of critical interest to identify the epigenetic patterns associated with adverse pregnancy outcomes. This review examines the potential role of DNA methylation as a risk factor for PTB and discusses several issues and limitations that should be considered when planning DNA methylation studies.
引用
收藏
页码:6 / 13
页数:8
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