机器学习根据人群肠道微生物组概况确定阿尔茨海默病的发病率。

IF 4.1 Q1 CLINICAL NEUROLOGY
Brain communications Pub Date : 2025-04-15 eCollection Date: 2025-01-01 DOI:10.1093/braincomms/fcaf059
Amedra Basgaran, Eva Lymberopoulos, Ella Burchill, Maryam Reis-Dehabadi, Nikhil Sharma
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引用次数: 0

摘要

人类微生物群是一个复杂而动态的微生物群落,被认为对其宿主具有共生利益。肠道微生物组对脑小胶质细胞的影响已被确定为神经退行性疾病的潜在机制,如阿尔茨海默病、运动神经元疾病和帕金森病(body SL, Giovannelli I, Sassani M,等)。肠道微生物群:在肌萎缩性侧索硬化症(ALS)的复杂性中起关键作用。中华医学会医学杂志,2013;19(1):13。我们假设肠道微生物组的人口水平差异将使用机器学习方法预测阿尔茨海默病的发病率。在R中使用两个大型开放获取的微生物组数据集(n = 959和n = 2012)进行横断面分析。这些数据集中的国家根据阿尔茨海默病的发病率和肠道微生物组的比较进行分组。在阿尔茨海默病高发的国家,肠道微生物群的多样性明显较低(P < 0.05)。方差检验的置换分析(P < 0.05)显示,在阿尔茨海默病发病率高与低的国家之间,微生物组谱存在显著差异,确定了几个贡献分类群:在物种水平上,大肠杆菌,在属水平上,发现嗜血杆菌和阿克曼氏菌在两个数据集中都具有可重复性保护作用。此外,使用机器学习,我们能够根据微生物组概况(曲线下平均面积0.889和0.927)预测一个国家内阿尔茨海默病的发病率。我们的结论是,微生物组的差异可以预测不同国家之间阿尔茨海默病的不同发病率。我们的研究结果支持肠道微生物组在人群水平上的神经变性中的关键作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Machine learning determines the incidence of Alzheimer's disease based on population gut microbiome profile.

The human microbiome is a complex and dynamic community of microbes, thought to have symbiotic benefit to its host. Influences of the gut microbiome on brain microglia have been identified as a potential mechanism contributing to neurodegenerative diseases, such as Alzheimer's disease, motor neurone disease and Parkinson's disease (Boddy SL, Giovannelli I, Sassani M, et al. The gut microbiome: A key player in the complexity of amyotrophic lateral sclerosis (ALS). BMC Med. 2021;19(1):13). We hypothesize that population level differences in the gut microbiome will predict the incidence of Alzheimer's disease using machine learning methods. Cross-sectional analyses were performed in R, using two large, open-access microbiome datasets (n = 959 and n = 2012). Countries in these datasets were grouped based on Alzheimer's disease incidence and the gut microbiome profiles compared. In countries with a high incidence of Alzheimer's disease, there is a significantly lower diversity of the gut microbiome (P < 0.05). A permutational analysis of variance test (P < 0.05) revealed significant differences in the microbiome profile between countries with high versus low incidence of Alzheimer's disease with several contributing taxa identified: at a species level Escherichia coli, and at a genus level Haemophilus and Akkermansia were found to be reproducibly protective in both datasets. Additionally, using machine learning, we were able to predict the incidence of Alzheimer's disease within a country based on the microbiome profile (mean area under the curve 0.889 and 0.927). We conclude that differences in the microbiome can predict the varying incidence of Alzheimer's disease between countries. Our results support a key role of the gut microbiome in neurodegeneration at a population level.

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