医学
队列
中心(范畴论)
病毒学
肝纤维化
内科学
纤维化
结晶学
化学
作者
Junhao Zha,Tianyi Xia,Zhi‐yuan Chen,Tianying Zheng,Shan Huang,Yu Qian,Jiaying Zhou,Peng Cao,Yuan‐cheng Wang,Tianyu Tang,Yang Song,Jun Xu,Bin Song,Yupin Liu,Shenghong Ju
摘要
Abstract Establishing reliable noninvasive tools to precisely diagnose clinically significant liver fibrosis (SF, ≥F2) remains an unmet need. We aimed to build a combined radiomics‐clinic (CoRC) model for triaging SF and explore the additive value of the CoRC model to transient elastography‐based liver stiffness measurement (FibroScan, TE‐LSM). This retrospective study recruited 595 patients with biopsy‐proven liver fibrosis at two centers between January 2015 and December 2021. At Center 1, the patients before December 2018 were randomly split into training (276) and internal test (118) sets, the remaining were time‐independent as a temporal test set (96). Another data set (105) from Center 2 was collected for external testing. Radiomics scores were built with selected features from Deep learning‐based (ResUNet) automated whole liver segmentations on MRI (T2FS and delayed enhanced‐T1WI). The CoRC model incorporated radiomics scores and relevant clinical variables with logistic regression, comparing routine approaches. Diagnostic performance was evaluated by the area under the receiver operating characteristic curve (AUC). The additive value of the CoRC model to TE‐LSM was investigated, considering necroinflammation. The CoRC model achieved AUCs of 0.79 (0.70, 0.86), 0.82 (0.73, 0.89), and 0.81 (0.72‐0.91), outperformed FIB‐4, APRI (all p < 0.05) in the internal, temporal, and external test sets and maintained the discriminatory power in G0‐1 subgroups (AUCs range, 0.85–0.86; all p < 0.05). The AUCs of joint CoRC‐LSM model were 0.86 (0.79–0.94), and 0.81 (0.72–0.90) in the internal and temporal sets ( p = 0.01). The CoRC model was useful for triaging SF, and may add value to TE‐LSM.
科研通智能强力驱动
Strongly Powered by AbleSci AI