The Microbiota-Gut-Brain Axis and Nutritional Interventions in Amyotrophic Lateral Sclerosis: Pathophysiological Mechanisms, Neuroinflammation, and Non-Motor Manifestations-Scoping Review.

Elena Sanchis-Sanchis, José Enrique de la Rubia Ortí, David Sancho-Cantus, Cristina Cunha-Pérez, Jorge Casaña-Mohedo
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Abstract

Amyotrophic Lateral Sclerosis (ALS) is a progressive neurodegenerative disorder in which systemic pathophysiological alterations significantly contribute to disease progression and non-motor manifestations, such as depression and anxiety. The microbiota-gut-brain axis represents a critical bidirectional pathway in which intestinal dysbiosis and epithelial barrier disruption catalyze central neuroinflammation. This scoping review synthesizes evidence from 43 empirical and analytical studies across 28 countries and maps the findings under the WHO International Classification of Functioning (ICF) framework. Pathophysiological data reveal a profound taxonomic shift in patients with ALS, characterized by severe depletion of neuroprotective, butyrate-producing genera (Akkermansia and Prevotella) and enrichment of pro-inflammatory Enterobacteriaceae. This dysbiotic state leads to structural damage to the intestinal mucosa, alteration of Paneth cells, and downregulation of tight junction proteins (zonulin), triggering a "leaky gut" phenomenon. Subsequent systemic translocation of lipopolysaccharides (LPS) induces TLR4-mediated endotoxemia, microglial hyperactivation, and accelerated motor neuron apoptosis. Conversely, therapeutic modulation via Fecal Microbiota Transplantation (FMT), psychobiotics, and metabolic interventions (ketogenic or Mediterranean diets) has demonstrated significant efficacy in restoring epithelial integrity, mitigating mitochondrial hypermetabolism, and reducing emotional distress. This review identifies a critical research gap in the microstructural characterization of the enteric nervous system in ALS. Incorporating microbiome-targeted biomarkers into clinical protocols is crucial for implementing a stratified, multi-systemic therapeutic strategy aimed at enhancing patient prognosis and psychological well-being.

肌萎缩性侧索硬化症的微生物-肠-脑轴和营养干预:病理生理机制,神经炎症和非运动表现-范围综述。
肌萎缩性侧索硬化症(ALS)是一种进行性神经退行性疾病,其全身病理生理改变显著促进疾病进展和非运动表现,如抑郁和焦虑。微生物-肠-脑轴是肠道生态失调和上皮屏障破坏催化中枢神经炎症的重要双向通路。这一范围审查综合了来自28个国家的43项实证和分析研究的证据,并在世卫组织国际功能分类框架下绘制了调查结果图。病理生理学数据显示,ALS患者的分类学发生了深刻的变化,其特征是神经保护、产生丁酸盐的属(Akkermansia和Prevotella)严重减少,而促炎肠杆菌科(proinflammatory Enterobacteriaceae)富集。这种生态失调状态导致肠黏膜结构损伤、Paneth细胞改变和紧密连接蛋白(zonulin)下调,从而引发“漏肠”现象。随后脂多糖(LPS)的全身性易位诱导tlr4介导的内毒素血症、小胶质细胞过度活化和加速运动神经元凋亡。相反,通过粪便微生物群移植(FMT)、精神生物制剂和代谢干预(生酮或地中海饮食)进行治疗调节已证明在恢复上皮完整性、减轻线粒体高代谢和减少情绪困扰方面具有显着功效。这篇综述确定了一个关键的研究空白在肠神经系统的微观结构表征的ALS。将微生物组靶向生物标志物纳入临床方案对于实施旨在提高患者预后和心理健康的分层、多系统治疗策略至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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