Faecal microbiome-based machine learning for multi-class disease diagnosis

Qi Su(Chinese University of Hong Kong), Qin Liu(Chinese University of Hong Kong), Raphaela Iris Lau(Chinese University of Hong Kong), Jingwan Zhang(Chinese University of Hong Kong), Zhilu Xu(Chinese University of Hong Kong), Yun Kit Yeoh, Thomas Leung(Chinese University of Hong Kong), Whitney Tang(Chinese University of Hong Kong), Lin Zhang(Chinese University of Hong Kong), Qiaoyi Liang(Chinese University of Hong Kong), Yuk Kam Yau(Chinese University of Hong Kong), Jiaying Zheng(Chinese University of Hong Kong), Chengyu Liu(Chinese University of Hong Kong), Mengjing Zhang(Chinese University of Hong Kong), Chun Pan Cheung(Chinese University of Hong Kong), Jessica Y. L. Ching(Chinese University of Hong Kong), Hein M. Tun(Chinese University of Hong Kong), Jun Yu(Chinese University of Hong Kong), Francis K.L. Chan(Chinese University of Hong Kong), Siew C. Ng(Chinese University of Hong Kong)
Nature Communications
November 10, 2022
Cited by 121Open Access
Full Text

Abstract

Systemic characterisation of the human faecal microbiome provides the opportunity to develop non-invasive approaches in the diagnosis of a major human disease. However, shared microbial signatures across different diseases make accurate diagnosis challenging in single-disease models. Herein, we present a machine-learning multi-class model using faecal metagenomic dataset of 2,320 individuals with nine well-characterised phenotypes, including colorectal cancer, colorectal adenomas, Crohn's disease, ulcerative colitis, irritable bowel syndrome, obesity, cardiovascular disease, post-acute COVID-19 syndrome and healthy individuals. Our processed data covers 325 microbial species derived from 14.3 terabytes of sequence. The trained model achieves an area under the receiver operating characteristic curve (AUROC) of 0.90 to 0.99 (Interquartile range, IQR, 0.91-0.94) in predicting different diseases in the independent test set, with a sensitivity of 0.81 to 0.95 (IQR, 0.87-0.93) at a specificity of 0.76 to 0.98 (IQR 0.83-0.95). Metagenomic analysis from public datasets of 1,597 samples across different populations observes comparable predictions with AUROC of 0.69 to 0.91 (IQR 0.79-0.87). Correlation of the top 50 microbial species with disease phenotypes identifies 363 significant associations (FDR < 0.05). This microbiome-based multi-disease model has potential clinical application in disease diagnostics and treatment response monitoring and warrants further exploration.


Related Papers