Circulating extracellular vesicle long RNA profiling combined with machine learning unveils novel diagnostic signature and molecular features in chronic pancreatitis

细胞外小泡 胰腺炎 随机森林 胞外囊泡 病理 医学 胰腺导管腺癌 疾病 生物信息学 机器学习 计算生物学 临床实习 人工智能 生物标志物 微阵列 核糖核酸 队列 表型 特征选择 生物 胰腺 折叠变化 训练集 转录组 逻辑回归 F1得分 相关性 无线电技术 接收机工作特性 分子生物标志物 外体 基因表达谱
作者
Yu Cao,Jia Hu,Jun Ye,Duowu Zou,Zheng Wang,Tao Yin,Wanxing Duan,Xuesong Liang,Jinying Chen,Y Li,Hongyan Lai,Shulin Yu,Zi Wang,Yuxing Wang,Peng Wang,Z Li,Wenbin Zou,Shenglin Huang,Zhuan Liao
出处
期刊:Gut [BMJ]
卷期号:: gutjnl-2025
标识
DOI:10.1136/gutjnl-2025-335957
摘要

BACKGROUND: No clinically useful non-invasive biomarkers have been developed for diagnosis of chronic pancreatitis (CP), and molecular features of CP have not been characterised. Extracellular vesicles (EVs) consisted of abundant RNA species with specialised functions and clinical applications. OBJECTIVE: Our study aimed to construct a diagnostic model for CP and depict molecular landscape of CP based on EV long RNA (ExLR). DESIGN: Candidate ExLRs were defined using prespecified expression-quality criteria and complementary discovery-stage screens, and a resampling-based consensus feature selection in the training cohort yielded a five-ExLRs panel for model construction. The ExLRs-based CP diagnostic model (ExLRCPdscore) was further confirmed in another two independent validation cohorts with different controls. To elucidate the biological architecture of CP through ExLR profiling, we integrated ExLR-seq, single-cell data and clinical information. RESULTS: ductal cells exhibiting the strongest correlation with CP and derived an ExLR-based acinar-to-ductal metaplasia (ADM) score as a blood-based transcriptomic proxy of ADM-related programme. Integration of ExLR-seq and clinical information revealed significant associations between ADMscore and clinical characteristics, imaging findings and metabolic sequelae. CONCLUSION: Our study is the first to report an ExLRs-based diagnostic model that demonstrates exceptional robustness in differentiating CP from healthy controls and non-pancreatic disease controls. ExLRs offer a promising tool for CP molecular characterisation and pathophysiological quantification.
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