Cambridge Baker Systems Genomics Initiative, Baker Heart and Diabetes Institute, Melbourne, VIC, Australia; Department of Clinical Pathology, Melbourne Medical School, The University of Melbourne, Melbourne, VIC, Australia.
Cambridge Baker Systems Genomics Initiative, Baker Heart and Diabetes Institute, Melbourne, VIC, Australia; Department of Clinical Pathology, Melbourne Medical School, The University of Melbourne, Melbourne, VIC, Australia; Baker Department of Cardiometabolic Health, The University of Melbourne, Melbourne, VIC, Australia; Department of Infectious Diseases, Central Clinical School, Monash University, Melbourne, VIC, Australia.
Cell Metab. 2022 May 3;34(5):719-730.e4. doi: 10.1016/j.cmet.2022.03.002. Epub 2022 Mar 29.
The gut microbiome has shown promise as a predictive biomarker for various diseases. However, the potential of gut microbiota for prospective risk prediction of liver disease has not been assessed. Here, we utilized shallow shotgun metagenomic sequencing of a large population-based cohort (N > 7,000) with ∼15 years of follow-up in combination with machine learning to investigate the predictive capacity of gut microbial predictors individually and in conjunction with conventional risk factors for incident liver disease. Separately, conventional and microbial factors showed comparable predictive capacity. However, microbiome augmentation of conventional risk factors using machine learning significantly improved the performance. Similarly, disease-free survival analysis showed significantly improved stratification using microbiome-augmented models. Investigation of predictive microbial signatures revealed previously unknown taxa for liver disease, as well as those previously associated with hepatic function and disease. This study supports the potential clinical validity of gut metagenomic sequencing to complement conventional risk factors for prediction of liver diseases.
肠道微生物组已显示出作为各种疾病预测性生物标志物的潜力。然而,肠道微生物群对肝病前瞻性风险预测的潜力尚未得到评估。在这里,我们利用大规模基于人群的队列(N > 7000)的浅层 shotgun 宏基因组测序,结合机器学习,研究了肠道微生物预测因子单独以及与常规风险因素对新发肝病的预测能力。单独来看,常规因素和微生物因素具有相当的预测能力。然而,使用机器学习对常规风险因素进行微生物组扩充显著提高了性能。同样,无病生存分析显示,使用微生物组扩充模型进行分层显著改善。对预测性微生物特征的研究揭示了以前未知的与肝脏疾病相关的分类群,以及以前与肝功能和疾病相关的分类群。本研究支持肠道宏基因组测序作为常规风险因素的补充,用于预测肝脏疾病的临床有效性。