Microbiota-gut-brain axis dysregulation in Alzheimer’s disease and its modulation through probiotic supplementation

益生菌 疾病 医学 调制(音乐) 免疫学 内科学 内分泌学 临床疾病 临床试验 生物信息学 药理学
作者
Moira Marizzoni,Elisa Mombelli,Silvia Alboni,Melissa Rosa,Davide Vito Moretti,Peppino Mirabelli,Luigi Coppola,Delia Luongo,Dominic Salamone,Samantha Saleri,Fabrizio Piazza,Veronica Begni,Marco Salvatore,Giovanni B. Frisoni,Annamaria Cattaneo
出处
期刊:Brain Behavior and Immunity [Elsevier BV]
卷期号:131: 106138-106138 被引量:1
标识
DOI:10.1016/j.bbi.2025.106138
摘要

BACKGROUND: The microbiota-gut-brain axis (MGBA) has been implicated in the pathophysiology of Alzheimer's Disease (AD).Probiotics reduced the progression of ADin different mouse models, possibly through MGBA modulation, but human data are still limited. OBJECTIVE: Here, we evaluated whether differences in the gut microbiome (GM), pro-inflammatory markers and other MGBA mediators were associated with probable AD (pAD). We also assessed the impact of a 12-week probiotic treatment on MGBA. METHODS: Forty-five pAD patients and 47 healthy subjects (HC) were recruited at IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli of Brescia (Italy). An uncontrolled clinical investigation was performed to test the effects of 12-week probiotic supplementation in the pAD group. Fecal microbiota composition, intestinal and blood inflammatory markers, and microbiota-related metabolites were assessed before supplementation in all participants and after only in pAD. RESULTS: pAD patients showed intestinal inflammation, an altered GM profile, blood changes in the tryptophan metabolism, and reduced glutamate levels compared with HC (p-value < 0.049). Probiotic supplementation partially modulated these alterations, determining a reduction in several pro-inflammatory mediators, and an increase of GM-related protective factors, such as butyrate (p-value < 0.040) in pAD. CONCLUSIONS: These findings confirmed the presence of MGBA alterations in AD and suggested a potential beneficial effect of probiotic supplementation through modulation of GM functionality rather than composition. Further research is required to confirm these results and their clinical relevance.
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