Exploring Interactions between Folate and Environmental Risk Factors for Autism

探索叶酸与自闭症环境风险因素之间的相互作用

• 批准号: 8628125
• 负责人: Rebecca Jean Schmidt
• 金额: $ 11.87万
• 依托单位: UNIVERSITY OF CALIFORNIA AT DAVIS
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-06-01 至 2016-02-29
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8628125
• 关键词: Address; Affect; Air Pollution; Animals; Attenuated; Autistic Disorder; Birth; California; Carbon; Child; Childhood; Communities; Complex; Conceptions; DNA Methylation; Databases; Development; Dose; Environment; Environmental Exposure; Environmental Policy; Environmental Risk Factor; Etiology; Fetus; Folate; Folic Acid; Genetic Risk; Household; Household Air Pollution; Infant; Intake; Interview; Investigation; Link; Measurable; Measures; Metabolic; Metabolism; Methylation; Modification; Mothers; Neurodevelopmental Disorder; Newborn Infant; Nutrient; Nutritional; Odds Ratio; Participant; Pathway interactions; Perinatal; Pesticides; Predisposition; Pregnancy; Prenatal Nutrition; Prospective Studies; Reporting; Research; Research Personnel; Risk; Risk Factors; Role; Structure; Supplementation; Testing; Time; Toxic Environmental Substances; United States; Vitamin B 12; Vitamin B Complex; Vitamin B6; Vitamins; Work; attenuation; autism spectrum disorder; base; disorder prevention; disorder risk; environmental agent; expectation; follow-up; high risk; methyl group; modifiable risk; mother nutrition; neonate; pesticide exposure; population based; prenatal; protective effect; pyrethroid; residence; trafficking

DESCRIPTION (provided by applicant): Autism spectrum disorder (ASD) is an increasingly prevalent neurodevelopmental disorder affecting 1:110 children in the United States. Evidence supports large heritable contributions to the etiology of ASD, though environmental factors are likely to modify both the development and the course of ASD. Prenatal nutrition and nutrient-environment interactions have been understudied in relation to autism etiology and risk. As the first researchers to examine maternal nutrition in association with autism risk, we found that mothers of children with autism were significantly less likely to report having taken prenatal vitamins around conception than mothers of typically developing (TD) children. Additionally, their estimated total folic acid intake was lower. Here it is proposed that maternal nutrient statu may contribute to the multifactorial etiology of autism by modifying susceptibility to other environmental agents. Animal studies show that folic acid supplementation can protect the fetus from environmental toxins through DNA methylation mechanisms. Thus, the overall purpose of this R21 is to examine interactions between nutrient status and environmental exposures in relation to ASD and to assess DNA methylation as a candidate mechanism for the modification of susceptibility. The focus is on two classes of environmental exposures that have been linked to increased ASD risk: traffic-related air pollution (TRP) and pesticides. Preliminary findings suggest attenuation of these associations from maternal periconceptional prenatal vitamin supplement intake. More specifically an investigation of whether two measures of folate status, maternally-reported folic acid intake and newborn bloodspot folate, act as effect modifiers for TRP and pesticides, while considering timing and dose or level of each exposure, and adjusting for confounders will be explored. Expectations here are that higher levels of folic acid before and during early pregnancy and neonate folate will reduce the risk of ASD associated with TRP and pesticide exposures in a dose-dependent manner. Further, an examination of global DNA methylation as a mechanism by which folate status may modify susceptibility to the environmental exposure effects will be tested. It is hypothesized that higher levels of folate will counter the neurodevelomentally relevant hypomethylation effects of these environmental exposures by providing abundant access to methyl-groups, (reflected in higher global DNA methylation levels in newborn bloodspots), and reducing their associated ASD risk. The proposed study will not only elucidate whether folate is able to reduce the neurodevelopmental consequences of harmful environmental exposures, but will also help reveal critical time periods and mechanisms behind potential protective effects. If the hypotheses are supported, this will be one of the first studies to identify complex relationships among modifiable risk factors for autism to be followed up in a prospective study, where we can assess timing, dose of exposures, and precise mechanisms more thoroughly. As such, it is likely to have a measurable impact on the scientific community, potentially on nutritional and environmental policies, and could potentially identify strategies for ASD prevention.

描述（由申请人提供）：自闭症谱系障碍（ASD）是一种日益普遍的神经发育障碍，影响美国1：110的儿童。证据支持ASD的病因学有很大的遗传贡献，尽管环境因素可能会改变ASD的发展和病程。产前营养和营养-环境相互作用与自闭症病因和风险的关系研究不足。作为第一个研究母亲营养与自闭症风险相关的研究人员，我们发现自闭症儿童的母亲在怀孕期间服用产前维生素的可能性明显低于正常发育（TD）儿童的母亲。此外，他们估计的叶酸总摄入量较低。在这里，它提出，母亲的营养状况可能有助于自闭症的多因素病因修改易感性，以其他环境因素。动物研究表明，补充叶酸可以通过DNA甲基化机制保护胎儿免受环境毒素的侵害。因此，R21的总体目的是研究营养状况和环境暴露与ASD之间的相互作用，并评估DNA甲基化作为易感性改变的候选机制。重点是与ASD风险增加有关的两类环境暴露：交通相关的空气污染（TRP）和农药。初步研究结果表明，这些协会从产妇围受孕产前维生素补充剂摄入衰减。更具体地说，将探讨叶酸状态的两个指标，母亲报告的叶酸摄入量和新生儿血斑叶酸，是否作为TRP和农药的效应调节剂，同时考虑每次暴露的时间和剂量或水平，并调整混杂因素。这里的期望是，在怀孕前和怀孕早期以及新生儿叶酸水平较高，将以剂量依赖性方式降低与TRP和农药暴露相关的ASD风险。此外，还将检测作为叶酸状态可能改变对环境暴露效应敏感性的机制的整体DNA甲基化。据推测，较高水平的叶酸将 通过提供大量的甲基基团（反映在新生儿血斑中较高的整体DNA甲基化水平），并降低其相关的ASD风险，来对抗这些环境暴露的神经发育相关的低甲基化效应。这项拟议的研究不仅将阐明叶酸是否能够减少有害环境暴露的神经发育后果，还将有助于揭示潜在保护作用背后的关键时间段和机制。如果这些假设得到支持，这将是第一个确定自闭症可改变的风险因素之间复杂关系的研究之一。 在一项前瞻性研究中，我们可以更彻底地评估暴露的时间，剂量和精确的机制。因此，它可能对科学界产生可衡量的影响，可能对营养和环境政策产生影响，并可能确定ASD预防策略。