a GMO and Mycotoxin Unit, Department of Food Safety, Nutrition and Veterinery Public Health , Istituto Superiore di Sanità , Viale Regina Elena, 299-00161 Roma , Italy.
b National Council of Research, Institute of Biomedical Technologies , Via f.lli Cervi 93, 20090 Segrate , MI , Italy.
Nutr Neurosci. 2019 Feb;22(2):132-144. doi: 10.1080/1028415X.2017.1357793. Epub 2017 Aug 10.
Gene-environment interaction is an emerging hypothesis to expound not only the autism pathogenesis but also the increased incidence of neurodevelopmental disorders (such as autistic spectrum disorder, attention-deficit, hyperactivity disorder). Among xenobiotics, mycotoxins are worldwide contaminants of food that provoke toxicological effects, crucially resembling several symptoms associated with autism such as oxidative stress, intestinal permeability, and inflammation. Here, we focused on a group of mycotoxins to test their role in the manifestation of autism, try to explain their mechanism of action, and discuss possible preventive and therapeutic interventions. Autistic children ( = 52) and healthy children [ = 58 (31 siblings and 27 unrelated subjects)] were recruited and body fluids and clinical data collected. The diagnosis of autism was made according to DSM V criteria, then with GMDS 0-2, WPPSI, and ADOS. Ochratoxin A (OTA), gliotoxin, zearalenone, and sphingosine/sphinganine ratio were determined by LC analysis in sera and urines. Statistical analysis was performed by the Wilcoxon Rank Sum (Mann-Whitney) test and Spearman test. By comparing the results of autistic patients with those of unrelated controls, a significant association was found for OTA levels in urines ( = 0.0002) and sera ( = 0.0017), and also comparing patients with siblings and unrelated controls together ( = 0.0081). Our results are the first describing a possible role of OTA in the pathobiology of autism. Recalling the male prevalence of ASD (male/female = 4-5/1), it is noted that, in animal models, OTA exerts its neurotoxicity especially in males. Moreover, , OTA increases microRNA-132 that is dysregulated in autistic patients and involved in reciprocal regulation of the autism-related genes MeCP2 and PTEN. A personalized diet coupled with probiotic administration, especially OTA adsorbing , could ameliorate autistic symptoms in OTA-positive patients.
基因-环境相互作用是一个新兴的假说,不仅可以解释自闭症的发病机制,还可以解释神经发育障碍(如自闭症谱系障碍、注意缺陷多动障碍)发病率的增加。在异源生物中,霉菌毒素是全世界食品污染物,会引发毒性作用,与自闭症的几种症状极为相似,如氧化应激、肠道通透性和炎症。在这里,我们集中研究了一组霉菌毒素,以测试它们在自闭症表现中的作用,尝试解释它们的作用机制,并讨论可能的预防和治疗干预措施。
我们招募了 52 名自闭症儿童和 58 名健康儿童[31 名兄弟姐妹和 27 名无血缘关系的受试者],收集了他们的体液和临床数据。自闭症的诊断是根据 DSM V 标准做出的,然后使用 GMDS 0-2、WPPSI 和 ADOS。血清和尿液中的黄曲霉毒素 A(OTA)、曲霉菌毒素、玉米赤霉烯酮和鞘氨醇/鞘氨醇比值通过 LC 分析进行测定。统计分析采用 Wilcoxon 秩和(Mann-Whitney)检验和 Spearman 检验。
通过比较自闭症患者和无血缘关系的对照组的结果,发现尿液( = 0.0002)和血清( = 0.0017)中的 OTA 水平以及将患者与兄弟姐妹和无血缘关系的对照组一起比较( = 0.0081)都存在显著相关性。
我们的结果是首次描述 OTA 在自闭症发病机制中的可能作用。考虑到 ASD 的男性患病率(男性/女性=4-5/1),值得注意的是,OTA 在动物模型中尤其对雄性具有神经毒性。此外,OTA 增加了在自闭症患者中失调的 microRNA-132,并且参与自闭症相关基因 MeCP2 和 PTEN 的相互调节。个性化饮食结合益生菌治疗,特别是 OTA 吸附剂,可以改善 OTA 阳性患者的自闭症症状。