Evidence map›Paper›PMID 42861201›Full record

ArticleDiabetes, metabolic syndrome and obesity : targets and therapy2026

Development of a Non-Invasive Prediction Model for MASLD Using Routine Clinical and Biochemical Markers: A Retrospective Study.

Lidan Dong, Jialian Zheng

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Article in Diabetes, metabolic syndrome and obesity : targets and therapy, 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

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2 authors.

Lidan DongHealth Examination Center, The First Hospital of Jiaxing (Affiliated Hospital of Jiaxing University), Jiaxing, Zhejiang, 314000, People's Republic of China.
Jialian ZhengHealth Examination Center, The First Hospital of Jiaxing (Affiliated Hospital of Jiaxing University), Jiaxing, Zhejiang, 314000, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Metabolic dysfunction-associated steatotic liver disease (MASLD), formerly known as non-alcoholic fatty liver disease, is a leading chronic liver condition associated with obesity and metabolic syndrome. Practical non-invasive models based on commonly available clinical and biochemical indicators may support risk stratification in health-check settings. Methods: This retrospective observational study included 8181 adults who underwent routine health examinations at the Health Examination Center of The First Hospital of Jiaxing from January 2024 to November 2024, including 4814 participants without MASLD and 3367 participants with ultrasound-reported hepatic steatosis after exclusion of secondary causes. Baseline comparisons, univariable logistic regression, multivariable logistic regression, Spearman correlation analysis, receiver operating characteristic (ROC) analysis, multicollinearity assessment, calibration assessment, and five-fold cross-validation were performed. Results: In the final model, older age, overweight, obesity, higher triglycerides, higher alanine aminotransferase, and higher uric acid were associated with higher odds of MASLD, whereas vitamin K was inversely associated with MASLD after adjustment. The final equation was logit(P) = -6.5363 + 0.0387 × age + 1.3838 × overweight + 2.6166 × obesity - 1.6016 × underweight + 1.0122 × triglycerides + 0.0267 × ALT + 0.0048 × uric acid - 0.1784 × vitamin K. The model achieved an AUC of 0.894 (95% CI 0.888-0.901). At the Youden-index cutoff of 0.402, sensitivity was 0.819 and specificity was 0.811. Five-fold cross-validation yielded a mean AUC of 0.894. Conclusion: A prediction model based on routine clinical and biochemical markers showed good discrimination for MASLD status in a single-center health examination cohort. Vitamin K was identified as an inversely associated exploratory marker, but this association should be interpreted cautiously and requires prospective and external validation before clinical or interventional conclusions can be drawn.

Indexed as

alanine aminotransferaseMASLDprediction modelroutine biomarkerstriglyceridesvitamin K

Identifiers

PMID42861201
PMCPMC13654284

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