Ramírez Viviana, González-Palacios Patricia, Baca Miguel A, González-Domenech Pablo José, Fernández-Cabezas María, Álvarez-Cubero María Jesús, Rodrigo Lourdes, Rivas Ana
Department of Nutrition and Food Science, Faculty of Pharmacy, University of Granada, 18071 Granada, Spain; GENYO. Centre for Genomics and Oncological Research: Pfizer / University of Granada / Andalusian Regional Government PTS Granada - Avenida de la Ilustración, 114, 18016 Granada, Spain; "José Mataix Verdú" Institute of Nutrition and Food Technology (INYTA), Biomedical Research Centre (CIBM), University of Granada, 18100 Granada, Spain.
Department of Nutrition and Food Science, Faculty of Pharmacy, University of Granada, 18071 Granada, Spain.
Sci Total Environ. 2022 Dec 15;852:158219. doi: 10.1016/j.scitotenv.2022.158219. Epub 2022 Aug 22.
Current evidence highlights the importance of the genetic component in obesity and neurodevelopmental disorders (attention-deficit hyperactivity disorder (ADHD), autism spectrum disorder (ASD) and intellectual disability (ID)), given that these diseases have reported an elevated heritability. Additionally, environmental stressors, such as endocrine disrupting chemicals (EDCs) have been classified as obesogens, neuroendocrine disruptors, and microbiota disrupting chemicals (MDCs). For this reason, the importance of this work lies in examining two possible biological mechanistic pathways linking obesity and neurodevelopmental/behavioural disorders: EDCs - gene and EDCs - microbiota interactions. First, we summarise the shared mechanisms of action of EDCs and the common genetic profile in the bidirectional link between obesity and neurodevelopment. In relation to interaction models, evidence from the reviewed studies reveals significant interactions between pesticides/heavy metals and gene polymorphisms of detoxifying and neurotransmission systems and metal homeostasis on cognitive development, ASD and ADHD symptomatology. Nonetheless, available literature about obesity is quite limited. Importantly, EDCs have been found to induce gut microbiota changes through gut-brain-microbiota axis conferring susceptibility to obesity and neurodevelopmental disorders. In view of the lack of studies assessing the impact of EDCs - gene interactions and EDCs - mediated dysbiosis jointly in obesity and neurodevelopment, we support considering genetics, EDCs exposure, and microbiota as interactive factors rather than individual contributors to the risk for developing obesity and neurodevelopmental disabilities at the same time.
目前的证据凸显了遗传因素在肥胖症以及神经发育障碍(注意力缺陷多动障碍(ADHD)、自闭症谱系障碍(ASD)和智力残疾(ID))中的重要性,因为这些疾病的遗传率较高。此外,环境压力源,如内分泌干扰化学物质(EDCs)已被归类为致肥胖物、神经内分泌干扰物和微生物群干扰化学物质(MDCs)。因此,这项工作的重要性在于研究将肥胖症与神经发育/行为障碍联系起来的两种可能的生物学机制途径:EDCs - 基因和EDCs - 微生物群相互作用。首先,我们总结了EDCs的共同作用机制以及肥胖症与神经发育双向联系中的共同基因特征。关于相互作用模型,综述研究的证据显示,农药/重金属与解毒和神经传递系统的基因多态性以及金属稳态之间在认知发展、ASD和ADHD症状方面存在显著相互作用。然而,关于肥胖症的现有文献相当有限。重要的是,已发现EDCs通过肠-脑-微生物群轴诱导肠道微生物群变化,从而使人易患肥胖症和神经发育障碍。鉴于缺乏评估EDCs - 基因相互作用和EDCs介导的生态失调对肥胖症和神经发育的联合影响的研究,我们支持将遗传学、EDCs暴露和微生物群视为相互作用的因素,而不是同时导致肥胖症和神经发育障碍风险的单独因素。