Dept. of Biochemistry and Molecular Medicine, The George Washington University School of Medicine and Health Sciences, 2300 Eye St., NW, Washington, DC 20037, United States.
Department of Clinical Chemistry, Medical Technology Branch, Faculty of Allied Health Sciences, Chulalongkorn University, 154 Rama I Rd., Wangmai, Pathumwan, Bangkok 10330, Thailand.
Horm Behav. 2018 May;101:13-21. doi: 10.1016/j.yhbeh.2017.10.003. Epub 2017 Oct 23.
Recent research on the etiology of autism spectrum disorder (ASD) has shifted in part from a singular focus on genetic causes to the involvement of environmental factors and their gene interactions. This shift in focus is a result of the rapidly increasing prevalence of ASD coupled with the incomplete penetrance of this disorder in monozygotic twins. One such area of environmentally focused research is the association of exposures to endocrine disrupting compounds (EDCs) with elevated risk for ASD. EDCs are exogenous chemicals that can alter endogenous hormone activity and homeostasis, thus potentially disrupting the action of sex and other natural hormones at all stages of human development. Inasmuch as sex hormones play a fundamental role in brain development and sexual differentiation, exposure to EDCs in utero during critical stages of development can have lasting neurological and other physiological influences on the developing fetus and, ultimately, the child as well as adult. This review will focus on the possible contributions of EDCs to autism risk and pathogenesis by first discussing the influence of endogenous sex hormones on the autistic phenotype, followed by a review of documented human exposures to EDCs and associations with behaviors relevant to ASD. Mechanistic links between EDC exposures and aberrant neurodevelopment and behaviors are then considered, with emphasis on EDC-induced transcriptional profiles derived from animal and cellular studies. Finally, this review will discuss possible mechanisms through which EDC exposure can lead to persistent changes in gene expression and phenotype, which may in turn contribute to transgenerational inheritance of ASD.
最近对自闭症谱系障碍(ASD)病因的研究部分从单一关注遗传原因转移到环境因素及其基因相互作用的参与。这种关注点的转变是由于 ASD 的患病率迅速增加,以及同卵双胞胎中这种疾病的不完全外显率所致。环境因素研究的一个领域是接触内分泌干扰化合物(EDCs)与 ASD 风险升高之间的关联。EDCs 是外源性化学物质,可以改变内源性激素活性和动态平衡,从而可能在人类发育的所有阶段破坏性激素和其他天然激素的作用。由于性激素在大脑发育和性分化中起着至关重要的作用,因此在发育关键阶段暴露于 EDC 会对发育中的胎儿产生持久的神经和其他生理影响,并最终对儿童以及成人产生影响。本综述将首先讨论内源性性激素对自闭症表型的影响,然后讨论已记录的人类接触 EDC 及其与 ASD 相关行为的关联,重点关注动物和细胞研究中源自 EDC 暴露的异常神经发育和行为的机制联系。最后,本综述将讨论 EDC 暴露可能导致基因表达和表型持久变化的可能机制,这可能反过来导致 ASD 的跨代遗传。