{"title":"Select Early-Life Environmental Exposures and DNA Methylation in the Placenta.","authors":"Michael Mortillo, Carmen J Marsit","doi":"10.1007/s40572-022-00385-1","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose of review: </strong>To summarize recent literature relating early-life environmental exposures on DNA methylation in the placenta, to identify how variation in placental methylation is regulated in an exposure-specific manner, and to encourage additional work in this area.</p><p><strong>Recent findings: </strong>Multiple studies have evaluated associations between prenatal environmental exposures and placental methylation in both gene-specific and epigenome-wide frameworks. Specific exposures lead to unique variability in methylation, and cross-exposure assessments have uncovered certain genes that demonstrate consistency in differential placental methylation. Exposure studies that assess methylation effects in a trimester-specific approach tend to find larger effects during the 1st trimester exposure. Earlier studies have more targeted gene-specific approaches to methylation, while later studies have shifted towards epigenome-wide, array-based approaches. Studies focusing on exposures such as air pollution, maternal smoking, environmental contaminants, and trace metals appear to be more abundant, while studies of socioeconomic adversity and circadian disruption are scarce but demonstrate remarkable effects. Understanding the impacts of early-life environmental exposures on placental methylation is critical to establishing the link between the maternal environment, epigenetic variation, and long-term health. Future studies into this field should incorporate repeated measures of exposure throughout pregnancy, in order to determine the critical windows in which placental methylation is most heavily affected. Additionally, the use of methylation-based scores and sequencing technology could provide important insights into epigenetic gestational age and uncovering more genomic regions where methylation is affected. Studies examining the impact of other exposures on methylation, including pesticides, alcohol, and other chemicals are also warranted.</p>","PeriodicalId":10775,"journal":{"name":"Current Environmental Health Reports","volume":"10 1","pages":"22-34"},"PeriodicalIF":7.4000,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10152976/pdf/nihms-1885407.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Environmental Health Reports","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s40572-022-00385-1","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/12/5 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose of review: To summarize recent literature relating early-life environmental exposures on DNA methylation in the placenta, to identify how variation in placental methylation is regulated in an exposure-specific manner, and to encourage additional work in this area.
Recent findings: Multiple studies have evaluated associations between prenatal environmental exposures and placental methylation in both gene-specific and epigenome-wide frameworks. Specific exposures lead to unique variability in methylation, and cross-exposure assessments have uncovered certain genes that demonstrate consistency in differential placental methylation. Exposure studies that assess methylation effects in a trimester-specific approach tend to find larger effects during the 1st trimester exposure. Earlier studies have more targeted gene-specific approaches to methylation, while later studies have shifted towards epigenome-wide, array-based approaches. Studies focusing on exposures such as air pollution, maternal smoking, environmental contaminants, and trace metals appear to be more abundant, while studies of socioeconomic adversity and circadian disruption are scarce but demonstrate remarkable effects. Understanding the impacts of early-life environmental exposures on placental methylation is critical to establishing the link between the maternal environment, epigenetic variation, and long-term health. Future studies into this field should incorporate repeated measures of exposure throughout pregnancy, in order to determine the critical windows in which placental methylation is most heavily affected. Additionally, the use of methylation-based scores and sequencing technology could provide important insights into epigenetic gestational age and uncovering more genomic regions where methylation is affected. Studies examining the impact of other exposures on methylation, including pesticides, alcohol, and other chemicals are also warranted.
综述的目的:总结与胎盘中 DNA 甲基化有关的早期环境暴露的最新文献,确定胎盘甲基化的变异是如何以暴露特异性的方式进行调节的,并鼓励在这一领域开展更多的工作:多项研究在基因特异性和全表观基因组框架内评估了产前环境暴露与胎盘甲基化之间的关联。特定的暴露会导致甲基化的独特变异,交叉暴露评估发现了某些基因在胎盘甲基化差异中表现出一致性。以特定孕期方法评估甲基化影响的暴露研究往往会发现,孕期前三个月的暴露影响较大。早期的研究更多地采用针对特定基因的甲基化方法,而后来的研究则转向基于整个表观基因组的阵列方法。针对空气污染、母体吸烟、环境污染物和痕量金属等暴露的研究似乎更多,而针对社会经济逆境和昼夜节律紊乱的研究很少,但却显示出显著的影响。了解生命早期环境暴露对胎盘甲基化的影响对于建立母体环境、表观遗传变异和长期健康之间的联系至关重要。未来在这一领域的研究应结合整个孕期暴露的重复测量,以确定胎盘甲基化受影响最严重的关键窗口期。此外,基于甲基化的评分和测序技术的使用可为表观遗传妊娠年龄提供重要见解,并揭示更多甲基化受影响的基因组区域。还需要研究其他暴露对甲基化的影响,包括杀虫剂、酒精和其他化学物质。
期刊介绍:
Current Environmental Health Reports provides up-to-date expert reviews in environmental health. The goal is to evaluate and synthesize original research in all disciplines relevant for environmental health sciences, including basic research, clinical research, epidemiology, and environmental policy.