A Deep Learning Model Based on High‐Frequency Ultrasound Images for Classification of Different Stages of Liver Fibrosis

肝纤维化 人工智能 医学 超声波 深度学习 纤维化 计算机科学 放射科 模式识别(心理学) 病理
作者
L.L. Zhang,Zhengbo Tan,Chunlei Li,Lichao Mou,Yufang Shi,Xiao Xiang Zhu,Yan Luo
出处
期刊:Liver International [Wiley]
卷期号:45 (7): e70148-e70148 被引量:5
标识
DOI:10.1111/liv.70148
摘要

ABSTRACT Background and Aims To develop a deep learning model based on high‐frequency ultrasound images to classify different stages of liver fibrosis in chronic hepatitis B patients. Methods This retrospective multicentre study included chronic hepatitis B patients who underwent both high‐frequency and low‐frequency liver ultrasound examinations between January 2014 and August 2024 at six hospitals. Paired images were employed to train the HF‐DL and the LF‐DL models independently. Three binary tasks were conducted: (1) Significant Fibrosis (S0‐1 vs. S2‐4); (2) Advanced Fibrosis (S0‐2 vs. S3‐4); (3) Cirrhosis (S0‐3 vs. S4). Hepatic pathological results constituted the ground truth for algorithm development and evaluation. The diagnostic value of high‐frequency and low‐frequency liver ultrasound images was compared across commonly used CNN networks. The HF‐DL model performance was compared against the LF‐DL model, FIB‐4, APRI, and with SWE (external test set). The calibration of models was plotted. The clinical benefits were calculated. Subgroup analysis for patients with different characteristics (BMI, ALT, inflammation level, alcohol consumption level) was conducted. Results The HF‐DL model demonstrated consistently superior diagnostic performance across all stages of liver fibrosis compared to the LF‐DL model, FIB‐4, APRI and SWE, particularly in classifying advanced fibrosis (0.93 [95% CI 0.90–0.95], 0.93 [95% CI 0.89–0.96], p < 0.01). The HF‐DL model demonstrates significantly improved performance in both target patient detection and negative population exclusion. Conclusions The HF‐DL model based on high‐frequency ultrasound images outperforms other routinely used non‐invasive modalities across different stages of liver fibrosis, particularly in advanced fibrosis, and may offer considerable clinical value.
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