# Early Detection of Liver Fibrosis Using Scatteromics Based on Multimodal QUS Envelope Statistics Imaging

**Authors:** Ya-Wen Chuang, Duy Chi Le, Chiao-Yin Wang, Dar-In Tai, Zhuhuang Zhou, Po-Hsiang Tsui

PMC · DOI: 10.3390/diagnostics16040564 · Diagnostics · 2026-02-13

## TL;DR

This study introduces a new ultrasound-based model to detect early liver fibrosis, even in patients with fatty liver disease, using advanced imaging techniques.

## Contribution

A simplified scatteromics model using multimodal QUS envelope statistics for early liver fibrosis detection in the presence of hepatic steatosis.

## Key findings

- Scatteromics features outperformed traditional QUS imaging in detecting early-stage liver fibrosis with AUROC values of 0.85-0.87.
- The model showed reduced dependence on AST and ALT levels, with low correlation coefficients (0.003-0.28).
- Performance was modest for significant fibrosis detection (≥F2), with AUROC values of 0.64-0.76.

## Abstract

Objectives: Radiomics has enhanced quantitative ultrasound (QUS) imaging based on envelope statistics for liver fibrosis evaluation. However, early detection of liver fibrosis in patients with hepatic steatosis remains challenging. This study is to develop ultrasound scatteromics prediction models, utilizing simplified feature sets from multimodal QUS envelope statistics imaging, for detecting early-stage liver fibrosis (stage ≥ F1) and significant fibrosis (≥F2) in the presence of hepatic steatosis. Methods: The dataset in this prospective study included 252 subjects (n = 125 for training and validation; n = 127 subjects for independent testing), which underwent blood tests, liver biopsy, and ultrasound radiofrequency data acquisition. In scatteromics analysis, multimodal QUS envelope statistics imaging (Nakagami, homodyned K, and information entropy statistics) was employed. For each imaging, a predefined simplified feature set was calculated, followed by feature selection for machine learning using support vector machine (SVM), random forest (RF), and linear discriminant analysis (LDA). The scatteromics model was obtained using a repeated five-fold stratified cross-validation and then independently tested. The performance was evaluated by the area under the receiver operating characteristic curve (AUROC); scatteromics features were also compared with aspartate aminotransferase (AST) and alanine aminotransferase (ALT). Results: Scatteromics features showed no significant correlation with AST and ALT, with correlation coefficients ranging from 0.003 to 0.28. In patients with coexisting hepatic steatosis, scatteromics significantly outperformed QUS envelope statistics imaging in identifying early-stage liver fibrosis, achieving AUROC values of 0.85 to 0.87 for the training and validation datasets, and 0.78 to 0.81 for the testing dataset. In comparison, scatteromics demonstrated modest performance in detecting significant liver fibrosis (≥F2), with AUROC ranging from 0.66 to 0.71 in the training cohort and 0.64 to 0.76 in the testing cohort. Conclusions: The proposed scatteromics model streamlines the data analysis workflow of conventional QUS radiomics, enabling early detection of liver fibrosis with reduced dependence on inflammation and hepatic steatosis.

## Full-text entities

- **Genes:** SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}
- **Diseases:** liver (MESH:D017093), liver damage (MESH:D056486), hepatocellular carcinoma (MESH:D006528), ascites (MESH:D001201), obesity (MESH:D009765), Hepatic steatosis (MESH:D005234), fat (MESH:D004620), Fibrosis (MESH:D005355), injury to (MESH:D014947), inflammation (MESH:D007249), chronic hepatitis (MESH:D006521), liver disease (MESH:D008107), Liver Fibrosis (MESH:D008103), cancer (MESH:D009369), Nonalcoholic fatty liver disease (MESH:D065626)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12939185/full.md

## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC12939185/full.md

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Source: https://tomesphere.com/paper/PMC12939185