Evidence map›Paper›PMID 42591968›Full record

ArticleTranslational pediatrics2026

An interpretable machine learning model based on routine clinical indicators for early identification of obesity-related non-alcoholic fatty liver disease in children: a single-center retrospective study.

Lili Zhuang, Jinxing Dai, Jiajia Wang, Qianjin Shi, Kang Shen, Hao Qiu, Weibing Qiu

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Article in Translational pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

7 authors.

Lili ZhuangDepartment of Pediatrics, Siyang Hospital, Suqian, China.
Jinxing DaiDepartment of Pediatrics, Siyang Hospital, Suqian, China.
Jiajia WangCancer Center, Siyang Hospital, Suqian, China.
Qianjin ShiCancer Center, Siyang Hospital, Suqian, China.
Kang ShenCancer Center, Siyang Hospital, Suqian, China.
Hao QiuCancer Center, Siyang Hospital, Suqian, China.
Weibing QiuDepartment of Pediatrics, Siyang Hospital, Suqian, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: There is still a lack of a noninvasive, individualized tool to pre-screen children with obesity for the risk of non-alcoholic fatty liver disease (NAFLD) and to prioritize referral for confirmatory abdominal ultrasonography. In this study, we aimed to develop and interpret a machine learning (ML)-based model for predicting ultrasound-defined NAFLD risk among children with obesity using routine clinical and biochemical indicators. Methods: This single-center retrospective study included 439 obese children treated at Siyang Hospital between February 2021 and December 2025. Demographic, anthropometric, and routine laboratory indicators were collected, and ultrasound-defined NAFLD was used as the study outcome. Least absolute shrinkage and selection operator (LASSO) regression and the Boruta algorithm were applied to identify robust predictive features, and six ML models-logistic regression, decision tree, random forest, extreme gradient boosting (XGBoost), light gradient boosting machine (LightGBM), and support vector machine (SVM)-were developed and compared to determine the optimal model. Model performance was evaluated in the test set, and Shapley Additive exPlanations (SHAP) was used to interpret the final model. Results: A total of 439 obese children were included in the analysis, of whom 206 (46.9%) had ultrasound-defined NAFLD. Seven variables were selected to develop six ML models. Among these, the LightGBM model showed the best overall performance across multiple metrics, with comparable discrimination among the top models in the test set, with an area under the curve (AUC) of 0.870, accuracy of 0.823, precision of 0.828, sensitivity of 0.787, specificity of 0.855, and F1 score of 0.807. SHAP analysis further demonstrated that waist-to-height ratio contributed most to the model output, followed by body mass index (BMI), triglyceride-glucose index × waist circumference (TyG-WC), serum uric acid, and triglyceride-glucose index × body mass index (TyG-BMI). Conclusions: This study developed an interpretable ML-based model for predicting ultrasound-defined NAFLD risk in obese children using routine clinical and biochemical indicators. LightGBM showed the best overall predictive performance, with good calibration and potential clinical utility. It may serve as a noninvasive auxiliary tool to pre-screen children with obesity and prioritize referral for confirmatory abdominal ultrasonography, supporting early identification and risk assessment of ultrasound-defined NAFLD, although further multicenter prospective studies and external validation are still needed before broader clinical application.

Indexed as

Childhood obesitylight gradient boosting machine (LightGBM)machine learning (ML)non-alcoholic fatty liver disease (NAFLD)Shapley Additive exPlanations (SHAP)

Identifiers

PMID42591968
PMCPMC13462896

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.