Petropoulos Andreas, Stavropoulou Elisavet, Tsigalou Christina, Bezirtzoglou Eugenia
Master Program in "Food, Nutrition and Microbiome", Laboratory of Hygiene and Environmental Protection, Department of Medicine, Democritus University of Thrace, 68100 Alexandroupolis, Greece.
Nutrients. 2025 Sep 17;17(18):2984. doi: 10.3390/nu17182984.
: Autism Spectrum Disorder (ASD) is a neurodevelopmental condition often accompanied by gastrointestinal (GI) symptoms and gut microbiota imbalances. The microbiota-gut-brain (MGB) axis is a bidirectional communication network linking gut microbes, the GI system, and the central nervous system (CNS). This narrative review explores the role of the MGB axis in ASD pathophysiology, focusing on communication pathways, neurodevelopmental implications, gut microbiota alteration, GI dysfunction, and emerging therapeutics. : A narrative review methodology was employed. We searched major scientific databases including PubMed, Scopus, and Google Scholar for research on MGB axis mechanisms, gut microbiota composition in ASD, dysbiosis, leaky gut, immune activation, GI disorders, and intervention (probiotics, prebiotics, fecal microbiota transplantation (FMT), antibiotics and diet). Key findings from recent human, animal and in vitro studies were synthesized thematically, emphasizing mechanistic insights and therapeutic outcomes. Original references from the initial manuscript draft were retained and supplemented for comprehensiveness and accuracy. : The MGB axis involves neuroanatomical, neuroendocrine, immunological, and metabolic pathways that enable microbes to influence brain development and function. Individuals with ASD commonly exhibit gut dysbiosis characterized by reduced microbial diversity (notably lower and ) and overpresentation of potentially pathogenic taxa (e.g., , , ). Dysbiosis is associated with increased intestinal permeability ("leaky gut") and newly activated and altered microbial metabolite profiles, such as short-chain fatty acids (SCFAs) and lipopolysaccharides (LPSs). Functional gastrointestinal disorders (FGIDs) are prevalent in ASD, linking gut-brain axis dysfunction to behavioral severity. Therapeutically, probiotics and prebiotics can restore eubiosis, fortify the gut barrier, and reduce neuroinflammation, showing modest improvements in GI and behavioral symptoms. FMT and Microbiota Transfer Therapy (MTT) have yielded promising results in open label trials, improving GI function and some ASD behaviors. Antibiotic interventions (e.g., vancomycin) have been found to temporarily alleviate ASD symptoms associated with overgrowth, while nutritional strategies (high-fiber, gluten-free, or ketogenic diets) may modulate the microbiome and influence outcomes. : Accumulating evidence implicates the MGB axis in ASD pathogenesis. Gut microbiota dysbiosis and the related GI pathology may exacerbate neurodevelopmental and behavioral symptoms via immune, endocrine and neural routes. Interventions targeting the gut ecosystem, through diet modification, probiotics, symbiotics, or microbiota transplants, offer therapeutic promise. However, heterogeneity in findings underscores the need for rigorous, large-scale studies to clarify causal relationships and evaluate long-term efficacy and safety. Understanding MGB axis mechanisms in ASD could pave the way for novel adjunctive treatments to improve the quality of life for individuals with ASD.
自闭症谱系障碍(ASD)是一种神经发育疾病,常伴有胃肠道(GI)症状和肠道微生物群失衡。微生物-肠道-脑(MGB)轴是一个双向通信网络,连接肠道微生物、胃肠道系统和中枢神经系统(CNS)。本叙述性综述探讨了MGB轴在ASD病理生理学中的作用,重点关注通信途径、神经发育影响、肠道微生物群改变、胃肠功能障碍和新兴治疗方法。
采用叙述性综述方法。我们在包括PubMed、Scopus和谷歌学术在内的主要科学数据库中搜索了关于MGB轴机制、ASD中的肠道微生物群组成、生态失调、肠漏、免疫激活、胃肠疾病和干预措施(益生菌、益生元、粪便微生物群移植(FMT)、抗生素和饮食)的研究。近期人类、动物和体外研究的主要发现进行了主题综合,强调了机制见解和治疗结果。保留了原始手稿初稿中的参考文献,并进行了补充以确保全面性和准确性。
MGB轴涉及神经解剖学、神经内分泌、免疫学和代谢途径,使微生物能够影响大脑发育和功能。ASD患者通常表现出肠道生态失调,其特征是微生物多样性降低(尤其是较低的 和 )以及潜在致病类群的过度呈现(例如 、 、 )。生态失调与肠道通透性增加(“肠漏”)以及新激活和改变的微生物代谢产物谱有关,如短链脂肪酸(SCFAs)和脂多糖(LPSs)。功能性胃肠疾病(FGIDs)在ASD中很常见,将肠-脑轴功能障碍与行为严重程度联系起来。在治疗方面,益生菌和益生元可以恢复正常微生物群,加强肠道屏障,并减少神经炎症,在胃肠和行为症状方面显示出适度改善。FMT和微生物群移植疗法(MTT)在开放标签试验中取得了有希望的结果,改善了胃肠功能和一些ASD行为。已发现抗生素干预措施(如万古霉素)可暂时缓解与 过度生长相关的ASD症状,而营养策略(高纤维、无麸质或生酮饮食)可能调节微生物群并影响治疗结果。
越来越多的证据表明MGB轴参与了ASD的发病机制。肠道微生物群生态失调和相关的胃肠病理学可能通过免疫、内分泌和神经途径加剧神经发育和行为症状。通过饮食调整、益生菌、共生菌或微生物群移植等针对肠道生态系统的干预措施具有治疗前景。然而,研究结果的异质性强调需要进行严格的大规模研究,以阐明因果关系并评估长期疗效和安全性。了解ASD中MGB轴的机制可能为新型辅助治疗铺平道路,以改善ASD患者的生活质量。