Nychas Emmanouil, Marfil-Sánchez Andrea, Chen Xiuqiang, Mirhakkak Mohammad, Li Huating, Jia Weiping, Xu Aimin, Nielsen Henrik Bjørn, Nieuwdorp Max, Loomba Rohit, Ni Yueqiong, Panagiotou Gianni
Department of Microbiome Dynamics, Leibniz Institute for Natural Product Research and Infection Biology - Hans Knöll Institute, Beutenbergstraße 11A, Jena, 07745, Germany.
Department of Endocrinology and Metabolism, Shanghai Clinical Center for Diabetes, Shanghai Key Laboratory of Diabetes Mellitus, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai Diabetes Institute, Shanghai, 200233, China.
Microbiome. 2025 Jan 14;13(1):10. doi: 10.1186/s40168-024-01990-y.
The pathogenesis of non-alcoholic fatty liver disease (NAFLD) with a global prevalence of 30% is multifactorial and the involvement of gut bacteria has been recently proposed. However, finding robust bacterial signatures of NAFLD has been a great challenge, mainly due to its co-occurrence with other metabolic diseases.
Here, we collected public metagenomic data and integrated the taxonomy profiles with in silico generated community metabolic outputs, and detailed clinical data, of 1206 Chinese subjects w/wo metabolic diseases, including NAFLD (obese and lean), obesity, T2D, hypertension, and atherosclerosis. We identified highly specific microbiome signatures through building accurate machine learning models (accuracy = 0.845-0.917) for NAFLD with high portability (generalizable) and low prediction rate (specific) when applied to other metabolic diseases, as well as through a community approach involving differential co-abundance ecological networks. Moreover, using these signatures coupled with further mediation analysis and metabolic dependency modeling, we propose synergistic defined microbial consortia associated with NAFLD phenotype in overweight and lean individuals, respectively.
Our study reveals robust and highly specific NAFLD signatures and offers a more realistic microbiome-therapeutics approach over individual species for this complex disease. Video Abstract.
非酒精性脂肪性肝病(NAFLD)的全球患病率为30%,其发病机制是多因素的,最近有人提出肠道细菌参与其中。然而,找到NAFLD可靠的细菌特征一直是一项巨大挑战,主要是因为它与其他代谢性疾病同时存在。
在此,我们收集了公开的宏基因组数据,并将分类学概况与计算机生成的群落代谢输出以及1206名患有或未患有代谢性疾病(包括NAFLD(肥胖和非肥胖)、肥胖症、2型糖尿病、高血压和动脉粥样硬化)的中国受试者的详细临床数据进行整合。我们通过构建准确的机器学习模型(准确率 = 0.845 - 0.917)来识别NAFLD高度特异性的微生物组特征,该模型在应用于其他代谢性疾病时具有高可移植性(可推广)和低预测率(特异性),并且通过涉及差异共丰度生态网络的群落方法来识别。此外,利用这些特征结合进一步的中介分析和代谢依赖性建模,我们分别提出了与超重和非肥胖个体中NAFLD表型相关的协同定义的微生物群落。
我们的研究揭示了可靠且高度特异性的NAFLD特征,并为这种复杂疾病提供了一种比针对单个物种更现实的微生物组治疗方法。视频摘要。