Tu Sha, Jing Xi, Bu Xiaoling, Zhang Qingfang, Liao Shanying, Zhu Xiaobo, Guo Ying, Sha Weihong
Department of Gastroenterology, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, 510080, People's Republic of China.
School of Nursing, Jinan University, Guangzhou, 510632, China.
Sci Rep. 2025 Apr 29;15(1):14944. doi: 10.1038/s41598-025-96158-5.
Despite advances in research, studies on predictive models for Non-Alcoholic Fatty Liver Disease (NAFLD)-related fibrosis remain limited. Identifying new biomarkers to distinguish Non-Alcoholic Steatohepatitis (NASH) from NAFLD would aid in the treatment of NASH. Gene expression and clinical profiles of NAFL and NASH patients were collected from databases. Differentially expressed genes with prognostic value were used to construct predictive model. Validation of fibrosis stage-related pyroptosis-related genes (PRGs) was performed using Sprague-Dawley rats liver fibrosis models induced by CCl4 or PS. Immune cell infiltration assessment demonstrated that stromal score, immune score, and ESTIMATE score were higher in patients with NASH compared to those with NAFL. BAX, BAK1, PYCARD, and NLRP3 were identified as hub genes that exhibit a strong correlation with fibrosis stage. Additionally, the expression of these genes was increased in fibrotic liver tissues induced by CCl4 and PS. The pyroptosis-associated gene signature effectively predicts the degree of liver fibrosis in NASH patients. Our study indicates that BAX, BAK1, PYCARD, and NLRP3 might serve as biomarkers for NASH-associated fibrosis.
尽管研究取得了进展,但关于非酒精性脂肪性肝病(NAFLD)相关纤维化预测模型的研究仍然有限。识别新的生物标志物以区分非酒精性脂肪性肝炎(NASH)和NAFLD将有助于NASH的治疗。从数据库中收集了NAFL和NASH患者的基因表达和临床资料。使用具有预后价值的差异表达基因构建预测模型。使用四氯化碳(CCl4)或硫代乙酰胺(PS)诱导的Sprague-Dawley大鼠肝纤维化模型对与纤维化阶段相关的焦亡相关基因(PRG)进行验证。免疫细胞浸润评估表明,与NAFL患者相比,NASH患者的基质评分、免疫评分和ESTIMATE评分更高。BAX、BAK1、PYCARD和NLRP3被确定为与纤维化阶段密切相关的枢纽基因。此外,这些基因在CCl4和PS诱导的纤维化肝组织中的表达增加。焦亡相关基因特征有效地预测了NASH患者的肝纤维化程度。我们的研究表明,BAX、BAK1、PYCARD和NLRP3可能作为NASH相关纤维化的生物标志物。