Development and internal validation of a diagnostic prediction model for advanced liver fibrosis based on routine laboratory indicators

Clicks: 13
ID: 331996
2026
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This article has not been analysed, so there is no overall score — reader engagement is measured and shown alongside.
AI Quality Assessment
Not analyzed
Readership in this journal
Emerging

Ranked #32 of 32 articles by views in Clinical chemistry and laboratory medicine

Most read Least read

Bar heights use a square-root scale.

Mint this article as an NFT
Not yet minted

Create a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.

5 SUSD one-off · no wallet required
Abstract
Abstract Introduction Advanced liver fibrosis is a clinically important stage of chronic liver disease. We developed and internally validated an interpretable model based on routine laboratory tests and benchmarked it against the aspartate aminotransferase to platelet ratio index (APRI) and 4-factor fibrosis index (FIB-4). Methods This single-center, retrospective, diagnostic prediction study included 1853 inpatients, of whom 988 had report-defined F3 to F4 fibrosis. Primary validation used 10 repeated, stratified 7:3 outer resamples, with preprocessing, least absolute shrinkage and selection operator selection, and model refitting restricted to each development subset. Discrimination, calibration, decision curves, precision recall performance, and linear SHapley Additive exPlanations values were evaluated. Results The leakage-aware pipeline achieved a mean (SD) validation area under the curve of 0.800 (0.015), accuracy of 0.753, sensitivity of 0.775, and specificity of 0.729. The final logistic model included platelet count, total bile acids, C3 and C4, red blood cell count, lymphocyte count, and albumin level. In the representative test set, its area under the curve was 0.809 (95% CI, 0.772-0.845) compared with 0.815 for APRI and 0.821 for FIB-4; neither paired difference was statistically significant after Holm adjustment. Discussion The model showed moderate discrimination and interpretable output but was not superior to APRI or FIB-4. External validation is required before clinical implementation.
Reference Key
openalex_W7221112388 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Junjie Deng, Wen Song, Yuyu Ma, Bin Fan, Xiumin Ma, Yumei Liu
Journal Clinical chemistry and laboratory medicine
Year 2026
DOI
10.1093/labmed/lmag053
URL
Keywords Keywords not found

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

No comments yet. Be the first to comment on this article.