Integration of Metabolomics, Lipidomics, and Machine Learning for Developing a Biomarker Panel to Distinguish the Severity of Metabolic-Associated Fatty Liver Disease.

Journal: Biomedical chromatography : BMC
Published Date:

Abstract

Metabolic-associated fatty liver disease (MAFLD), a global health challenge linked to metabolic syndrome, requires accurate severity stratification for clinical management. Current invasive diagnostic methods limit practical implementation. This study integrated multi-omics and machine learning to establish a non-invasive biomarker panel for the early stage of MAFLD assessment. Transcriptomic analysis of GEO datasets via weighted gene co-expression network (WGCNA) and differential expression revealed critical pathways associated with MAFLD progression. Subsequently, LC-MS/MS-based widely targeted metabolomics and lipidomics were conducted on plasma samples from 40 healthy controls and 120 patients with MAFLD at varying stages of severity (40 mild, 40 moderate, and 40 severe). Machine learning algorithms (LASSO regression, logistic regression, decision trees, and XGBoost) were then applied to these datasets to identify critical biomarkers linked to disease severity. Ultimately, a biomarker panel comprising 5-aminolevulinic acid, mesaconic acid, shikimic acid, PC O-35:3, and PI 36:2 exhibited outstanding diagnostic performance in detecting the prevalence and severity of MAFLD, achieving an accuracy of 88.3% in the training cohort and over 91.7% prediction accuracy in the independent test cohort. The identified biomarker panel offers a promising non-invasive approach for assessing MAFLD severity, paving the way for precision medicine and treatment in MAFLD.

Authors

  • Yanqiao Hui
    School of Pharmacy, Shenyang Pharmaceutical University, Shenyang, China.
  • Jiameng Qu
    School of Pharmacy, Shenyang Pharmaceutical University, Shenyang, China.
  • Junjie Yang
    School of Automation Science and Engineering, Xian Jiaotong University, Xi'an, Shaanxi, China.
  • Hanwen Zhang
    Department of Radiology, The First Affiliated Hospital of Shenzhen University, Health Science Center, Shenzhen Second People's Hospital, Shenzhen, China.
  • Chen Liang
    Shanghai Institute of Forensic Science, Shanghai Key Laboratory of Crime Scene Evidence, Shanghai 200083, China.
  • Naixin Miao
    School of Pharmacy, Shenyang Pharmaceutical University, Shenyang, China.
  • Qian Zhang
    The Neonatal Intensive Care Unit, Peking Union Medical College Hospital, Peking, China.
  • Huarong Xu
    School of Pharmacy, Shenyang Pharmaceutical University, Shenyang, China.
  • Yiling Li
    Department of Gastroenterology, The First Hospital of China Medical University, Shenyang, PR China. Electronic address: lyl-72@163.com.
  • Qing Li
    Department of Internal Medicine, University of Michigan Ann Arbor, MI 48109, USA.