Center for Environmental and Health Sciences, Hokkaido University.
Health Center, Chuo University.
Environ Health Prev Med. 2022;27:24. doi: 10.1265/ehpm.21-00033.
There are only limited numbers of reviews on the association of maternal-child genetic polymorphisms and environmental and lifestyle-related chemical exposure during pregnancy with adverse fetal growth. Thus, this article aims to review: (1) the effect of associations between the above highlighted factors on adverse fetal growth and (2) recent birth cohort studies regarding environmental health risks.
Based on a search of the PubMed database through August 2021, 68 epidemiological studies on gene-environment interactions, focusing on the association between environmental and lifestyle-related chemical exposure and adverse fetal growth was identified. Moreover, we also reviewed recent worldwide birth cohort studies regarding environmental health risks.
Thirty studies examined gene-smoking associations with adverse fetal growth. Sixteen maternal genes significantly modified the association between maternal smoking and adverse fetal growth. Two genes significantly related with this association were detected in infants. Moreover, the maternal genes that significantly interacted with maternal smoking during pregnancy were cytochrome P450 1A1 (CYP1A1), X-ray repair cross-complementing protein 3 (XRCC3), interleukin 6 (IL6), interleukin 1 beta (IL1B), human leukocyte antigen (HLA) DQ alpha 1 (HLA-DQA1), HLA DQ beta 1 (HLA-DQB1), and nicotinic acetylcholine receptor. Fetal genes that had significant interactions with maternal smoking during pregnancy were glutathione S-transferase theta 1 (GSTT1) and fat mass and obesity-associated protein (FTO). Thirty-eight studies examined the association between chemical exposures and adverse fetal growth. In 62 of the 68 epidemiological studies (91.2%), a significant association was found with adverse fetal growth. Across the studies, there was a wide variation in the analytical methods used, especially with respect to the genetic polymorphisms of interest, environmental and lifestyle-related chemicals examined, and the study design used to estimate the gene-environment interactions. It was also found that a consistently increasing number of European and worldwide large-scale birth cohort studies on environmental health risks have been conducted since approximately 1996.
There is some evidence to suggest the importance of gene-environment interactions on adverse fetal growth. The current knowledge on gene-environment interactions will help guide future studies on the combined effects of maternal-child genetic polymorphisms and exposure to environmental and lifestyle-related chemicals during pregnancy.
目前仅有少量研究探讨了孕产妇遗传多态性与妊娠期间环境和生活方式相关化学暴露之间的关联,以及这些关联对胎儿生长不良的影响。因此,本文旨在综述:(1)上述重点因素的关联对胎儿生长不良的影响;(2)近期有关环境健康风险的出生队列研究。
本研究基于 2021 年 8 月之前在 PubMed 数据库中进行的检索,共确定了 68 项关于基因-环境相互作用的流行病学研究,重点探讨了环境和生活方式相关化学暴露与胎儿生长不良之间的关联。此外,我们还综述了近期有关环境健康风险的全球出生队列研究。
有 30 项研究探讨了基因-吸烟与胎儿生长不良之间的关联。16 个母体基因显著改变了母体吸烟与胎儿生长不良之间的关联。在婴儿中发现了两个与这种关联显著相关的基因。此外,在妊娠期间与母体吸烟显著相互作用的母体基因有细胞色素 P450 1A1(CYP1A1)、X 射线修复交叉互补蛋白 3(XRCC3)、白细胞介素 6(IL6)、白细胞介素 1β(IL1B)、人类白细胞抗原(HLA)DQα1(HLA-DQA1)、HLA DQβ1(HLA-DQB1)和烟碱型乙酰胆碱受体。在妊娠期间与母体吸烟显著相互作用的胎儿基因有谷胱甘肽 S-转移酶 theta 1(GSTT1)和脂肪量和肥胖相关蛋白(FTO)。有 38 项研究探讨了化学暴露与胎儿生长不良之间的关联。在 68 项流行病学研究中的 62 项(91.2%)中,发现了与胎儿生长不良之间的显著关联。在这些研究中,所用的分析方法存在很大差异,尤其是在关注的遗传多态性、环境和生活方式相关化学物质以及用于估计基因-环境相互作用的研究设计方面。此外,自 1996 年以来,一直有越来越多的欧洲和全球规模的出生队列研究针对环境健康风险展开。
有证据表明基因-环境相互作用对胎儿生长不良的重要性。目前对基因-环境相互作用的认识将有助于指导未来对孕产妇-儿童遗传多态性与妊娠期间环境和生活方式相关化学暴露的综合影响的研究。