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Faecal microbiome-based machine learning for multi-class disease diagnosis.
Su, Qi; Liu, Qin; Lau, Raphaela Iris; Zhang, Jingwan; Xu, Zhilu; Yeoh, Yun Kit; Leung, Thomas W H; Tang, Whitney; Zhang, Lin; Liang, Jessie Q Y; Yau, Yuk Kam; Zheng, Jiaying; Liu, Chengyu; Zhang, Mengjing; Cheung, Chun Pan; Ching, Jessica Y L; Tun, Hein M; Yu, Jun; Chan, Francis K L; Ng, Siew C.
  • Su Q; Microbiota I-Center (MagIC), Hong Kong SAR, China.
  • Liu Q; Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Lau RI; Li Ka Shing Institute of Health Sciences, State Key Laboratory of Digestive Disease, Institute of Digestive Disease, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Zhang J; Center for Gut Microbiota Research, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Xu Z; Microbiota I-Center (MagIC), Hong Kong SAR, China.
  • Yeoh YK; Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Leung TWH; Li Ka Shing Institute of Health Sciences, State Key Laboratory of Digestive Disease, Institute of Digestive Disease, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Tang W; Center for Gut Microbiota Research, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Zhang L; Microbiota I-Center (MagIC), Hong Kong SAR, China.
  • Liang JQY; Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Yau YK; Li Ka Shing Institute of Health Sciences, State Key Laboratory of Digestive Disease, Institute of Digestive Disease, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Zheng J; Microbiota I-Center (MagIC), Hong Kong SAR, China.
  • Liu C; Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Zhang M; Li Ka Shing Institute of Health Sciences, State Key Laboratory of Digestive Disease, Institute of Digestive Disease, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Cheung CP; Center for Gut Microbiota Research, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Ching JYL; Microbiota I-Center (MagIC), Hong Kong SAR, China.
  • Tun HM; Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Yu J; Li Ka Shing Institute of Health Sciences, State Key Laboratory of Digestive Disease, Institute of Digestive Disease, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Chan FKL; Center for Gut Microbiota Research, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Ng SC; Microbiota I-Center (MagIC), Hong Kong SAR, China.
Nat Commun ; 13(1): 6818, 2022 Nov 10.
Article in English | MEDLINE | ID: covidwho-2117855
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.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Microbiota / COVID-19 Type of study: Diagnostic study / Prognostic study Topics: Long Covid Limits: Humans Language: English Journal: Nat Commun Journal subject: Biology / Science Year: 2022 Document Type: Article Affiliation country: S41467-022-34405-3

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Microbiota / COVID-19 Type of study: Diagnostic study / Prognostic study Topics: Long Covid Limits: Humans Language: English Journal: Nat Commun Journal subject: Biology / Science Year: 2022 Document Type: Article Affiliation country: S41467-022-34405-3