OBJECTIVE: Early intervention in metabolic dysfunction-associated steatohepatitis (MASH) is critical to halt disease progression. However, noninvasive tools for monitoring early-stage MASH and therapeutic efficacy in preclinical models remain limited, impeding preclinical drug development. This study establishes an integrated approach using multiparametric magnetic resonance imaging (MRI) at 9.4 T to dynamically track disease development and drug response in a prefibrotic MASH mouse model. MATERIALS AND METHODS: mapping, and diffusion-weighted imaging (DWI)-were performed every 4 weeks and correlated with histopathology. RESULTS: by 46% (p < 0.001), and ADC increased 1.4-fold (p = 0.017) compared to the vehicle group. CONCLUSION: This work demonstrates multiparametric MRI as a powerful noninvasive platform for monitoring early MASH dynamics and treatment response. By enabling longitudinal assessment in a prefibrotic model, this approach accelerates translational research in MASH diagnosis and drug development. RELEVANCE STATEMENT: The established multiparametric MRI evaluation system provides a valuable noninvasive monitoring platform for preclinical early-stage MASH research, demonstrating significant potential to accelerate the translational progress in MASH diagnosis and drug development. KEY POINTS: A novel prefibrotic MASH model was established to assess early-stage MASH progression. Multiparametric MRI at 9.4 T enables noninvasive, longitudinal monitoring of early MASH. Semaglutide-induced improvement in steatosis and inflammation can be monitored by multiparametric MRI.
Building similarity graph...
Analyzing shared references across papers
Loading...
Yuanyuan Li
Y N Wu
Gengxin Wang
European Radiology Experimental
University of Science and Technology of China
Suzhou Research Institute
Suzhou University of Science and Technology
Building similarity graph...
Analyzing shared references across papers
Loading...
Li et al. (Wed,) studied this question.
www.synapsesocial.com/papers/69fd7f4fbfa21ec5bbf07ced — DOI: https://doi.org/10.1186/s41747-026-00719-w