Noninvasive Assessment of Liver Fibrosis and Inflammation in Chronic Hepatitis B: A Dual-task Convolutional Neural Network (DtCNN) Model Based on Ultrasound Shear Wave Elastography

被引:6
|
作者
Wang, Chengyan [1 ]
Zheng, Lili [2 ]
Li, Yan [3 ]
Xia, Shujun [4 ]
Lv, Jun [5 ]
Hu, Xumei [1 ]
Zhan, Weiwei [4 ]
Yan, Fuhua [3 ]
Li, Ruokun [3 ]
Ren, Xinping [4 ]
机构
[1] Fudan Univ, Human Phenome Inst, Shanghai, Peoples R China
[2] Shanghai Jiao Tong Univ, Ruijin Hosp, Sch Med, Wuxi Branch,Ultrasound Dept, Wuxi, Jiangsu, Peoples R China
[3] Shanghai Jiao Tong Univ, Ruijin Hosp, Sch Med, Dept Radiol, 197 Ruijin 2nd Rd, Shanghai 200020, Peoples R China
[4] Shanghai Jiao Tong Univ, Ruijin Hosp, Sch Med, Ultrasound Dept, 197 Ruijin 2nd Rd, Shanghai 200020, Peoples R China
[5] Yantai Univ, Sch Comp & Control Engn, Yantai, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Fibrosis; Inflammation; Shear wave elastography; Chronic hepatitis B; Dual-task convolutional neural network; IMPULSE ELASTOGRAPHY; CLASSIFICATION; VARIABILITY; STIFFNESS; CIRRHOSIS; ACCURACY; BIOPSY; US;
D O I
10.14218/JCTH.2021.00447
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and Aims: Liver stiffness (LS) measured by shear wave elastography (SWE) is often influenced by hepatic inflammation. The aim was to develop a dual-task convolutional neural network (DtCNN) model for the simultaneous staging of liver fibrosis and inflammation activity using 2DSWE. Methods: A total of 532 patients with chronic hepatitis B (CHB) were included to develop and validate the DtCNN model. An additional 180 consecutive patients between December 2019 and April 2021 were prospectively included for further validation. All patients underwent 2D-SWE examination and serum biomarker assessment. A DtCNN model containing two pathways for the staging of fibrosis and inflammation was used to improve the classification of significant fibrosis (>= F2), advanced fibrosis (>= F3) as well as cirrhosis (F4). Results: Both fibrosis and inflammation affected LS measurements by 2D-SWE. The proposed DtCNN performed the best among all the classification models for fibrosis stage [significant fibrosis AUC=0.89 (95% CI: 0.87-0.92), advanced fibrosis AUC=0.87 (95% CI: 0.84-0.90), liver cirrhosis AUC=0.85 (95% CI: 0.81-0.89)]. The DtCNN-based prediction of inflammation activity achieved AUCs of 0.82 (95% CI: 0.78-0.86) for grade >= A1, 0.88 (95% CI: 0.85-0.90) grade >= A2 and 0.78 (95% CI: 0.75-0.81) for grade >= A3, which were significantly higher than the AUCs of the singletask groups. Similar findings were observed in the prospective study. Conclusions: The proposed DtCNN improved diagnostic performance compared with existing fibrosis staging models by including inflammation in the model, which supports its potential clinical application.
引用
收藏
页码:1077 / 1085
页数:9
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