Abstract
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.
Original language | English (US) |
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Pages (from-to) | 6-13 |
Number of pages | 8 |
Journal | Reproductive Sciences |
Volume | 19 |
Issue number | 1 |
DOIs | |
State | Published - Jan 2012 |
Keywords
- DNA
- epigenetics
- genetics
- prematurity
- preterm labor
ASJC Scopus subject areas
- Obstetrics and Gynecology