Key result
Online dynamic nomogram identifies nonobese MASLD with ~0.80 validation AUC using clinical and body metrics.
Why the study?
Does an online dynamic nomogram based on body composition analysis and blood biochemical indicators accurately identify nonobese metabolic dysfunction-associated steatotic liver disease (MASLD) in adults with BMI < 24 kg/m²?
Cross-Sectional (n=538)
No
Does an online dynamic nomogram based on body composition analysis and blood biochemical indicators accurately identify nonobese metabolic dysfunction-associated steatotic liver disease (MASLD) in adults with BMI < 24 kg/m²?
Answers are grounded in this paper and cite their sources.
This study provides an accessible online dynamic nomogram combining routine lipid profiles, metabolic history, and bioelectrical impedance body composition parameters to screen for MASLD in non-obese individuals who might otherwise be overlooked due to normal BMI.
BACKGROUND: The factors influencing nonobese Metabolic dysfunction-associated steatotic liver disease are discussed, and an online dynamic nomogram model is constructed. METHODS: A retrospective analysis was conducted on the clinical data of 216 non-obese patients with MASLD and 322 non-obese healthy controls from the Second Affiliated Hospital of Soochow University. The data were randomly divided into a training set and a validation set in a 7:3 ratio. Potential variables were initially screened through univariate analysis, correlation analysis, and LASSO regression (including cross-validation). Subsequently, binary logistic regression and SHAP methods were employed to identify independent risk factors, and an online dynamic ROC curve was constructed. Model performance was evaluated using the area under the curve (AUC), sensitivity, specificity, calibration curves, and recalibration methods. RESULTS: LASSO regression initially screened 11 potential variables. Binary logistic regression ultimately identified six independent risk factors which is past history (odds ratio (OR): 2.399, P = 0.0008), triglyceride(TG) (OR: 1.176, P = 0.008), high density lipoprotein cholesterol(HDL-C) (OR: 0.173, P = 0.014), low density lipoprotein cholesterol(LDL-C) (OR: 3.916, P = 0.001), fat mass(Fat) (OR: 4.299, P = 0.0009) and dPhaseAngle(OR: 3.174, P = 0.022). SHAP analysis revealed that TG was the most influential feature, while HDL-C showed a negative contribution. All variance inflation factor (VIF) values were below 1.5, indicating no significant multicollinearity. The AUC values were 0.869 in the training cohort and 0.802 in the validation cohort. The calibration curve demonstrates that the prediction results of the line graph for the outcome closely approximate the ideal curve, aligning with the actual outcomes. CONCLUSION: An online dynamic nomogram for nonobese MASLD patients with good identified performance was constructed, which can be used as a practical approach for personalized early screening and auxiliary diagnosis of potential risk factors and can assist physicians in making personalized diagnoses and treatments for patients.
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Zheng et al. (2026) conducted a cross-sectional in Nonobese metabolic dysfunction-associated steatotic liver disease (MASLD) (n=538). Online dynamic nomogram based on six independent predictors (past metabolic history, TG, HDL-C, LDL-C, fat mass, and dPhaseAngle) vs. Non-obese healthy controls without MASLD was evaluated on Diagnostic identification of nonobese MASLD (AUC 0.802 in validation cohort (AUC 0.869 in training cohort), 95% CI 0.734-0.870). An online dynamic nomogram incorporating six clinical and body composition predictors identified nonobese MASLD with an AUC of 0.869 in the training cohort and 0.802 in the validation cohort.
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