Related Experiment Video For Advanced colorectal neoplasia
Updated: Jun 3, 2026

Mouse Model of Metabolic Dysfunction-Associated Steatotic Liver Disease with Fibrosis
Published on: July 18, 2025
Advanced colorectal neoplasia and colorectal cancer in metabolic dysfunction-associated steatotic liver disease
Qin-Fen Chen1, Wei Xie2, Haojun Cai3
1Medical Care Center, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, China; Wenzhou Key Laboratory of Intelligent Prevention and Active Health for Aging-Related Chronic Diseases, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, China; Institute of Aging, Wenzhou Medical University, Wenzhou 325000, China.
Background:
Although metabolic-associated fatty liver disease (MASLD) is linked to an increased prevalence of colorectal cancer (CRC), large-scale incidence data on its association with advanced colorectal neoplasia (ACN) and CRC are lacking.
Objective:
This retrospective longitudinal study aims to evaluate the association between MASLD and the incidence of ACN and CRC.
Methods:
Three populations were used from a large-scale health check-up cohort: 127,344 individuals for initial colonoscopy screening (prevalence of ACN and CRC), 77,316 individuals with clinical follow-up (incidence of CRC), and 25,694 individuals with follow-up colonoscopy (incidence of ACN and CRC). Cox regression and Kaplan-Meier analysis were performed, stratified by liver fibrosis severity using the Fibrosis-4 index.
Results:
Among 127,344 participants undergoing colonoscopy, 8.3% had ACN and 3.4% had CRC. MASLD was associated with a higher prevalence of both (10.7% vs. 7.0%, P < 0.001; 3.9% vs. 3.1%, P < 0.001) and increased risk of ACN (OR = 1.55, 95% CI: 1.47-1.63) and CRC (OR = 1.41, 95% CI: 1.31-1.53). Among 77,316 individuals followed for a median of 4.0 years, MASLD was associated with a higher CRC incidence (1.9 vs. 1.1 per 1,000 person-years; HR = 2.11, 95% CI: 1.71-2.61). In 25,694 individuals with follow-up colonoscopy, MASLD increased the risk of ACN (HR = 1.89, 95% CI: 1.61-2.21) and CRC (HR = 1.64, 95% CI: 1.17-2.30). Across all analyses, more severe fibrosis was associated with progressively higher risks. Sensitivity and subgroup analyses further confirmed the robustness of the outcomes.
Conclusion:
MASLD is associated with a higher prevalence and incidence of CRC and ACN, with risks increasing stepwise with liver fibrosis severity.
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