Construction and validation of a risk prediction model for lean metabolic dysfunction-associated steatotic liver disease

Objective‍ ‍To investigate the risk factors for the occurrence of metabolic dysfunction-associated steatotic liver disease(MASLD) in lean individuals and construct a risk prediction model. Methods‍ ‍Based on the National Health and Nutrition Examination Survey(NHANES) database in the United States(f...

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Main Authors: QIN Jiayi, ZHOU Xueqian, MENG Xiangyong
Format: Article
Language:zho
Published: Editorial Office of Journal of Army Medical University 2025-05-01
Series:陆军军医大学学报
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Online Access:https://aammt.tmmu.edu.cn/html/202412024.html
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author QIN Jiayi
ZHOU Xueqian
MENG Xiangyong
author_facet QIN Jiayi
ZHOU Xueqian
MENG Xiangyong
author_sort QIN Jiayi
collection DOAJ
description Objective‍ ‍To investigate the risk factors for the occurrence of metabolic dysfunction-associated steatotic liver disease(MASLD) in lean individuals and construct a risk prediction model. Methods‍ ‍Based on the National Health and Nutrition Examination Survey(NHANES) database in the United States(from January 2017 to March 2020), 1 123 adult individuals were included in this study. Then the participants were randomly divided into a training set(n=561) and a validation set(n=562) through simple random sampling. Data on their demographics, anthropometrics, lifestyle, underlying diseases, and laboratory test results were collected. LASSO regression analysis was used to screen potential variables in the training set, and multivariate logistic regression was employed to identify independent risk factors for lean MASLD. Based on these risk factors, a prediction model for lean MASLD was constructed(LMPM). To evaluate the clinical value of the LMPM, it was compared with two commonly used prediction models for non-alcoholic fatty liver disease, the fatty liver index(FLI) and the hepatic steatosis index(HSI). The performance of the model was evaluated and internally validated using the area under the receiver operating characteristic curve(AUC), net reclassification index(NRI), integrated discrimination improvement(IDI), calibration curve, decision curve, and clinical impact curve. Results‍ ‍Age, waist circumference, and triglycerides(TG) were identified as independent risk factors for the development of MASLD in lean individuals. The LMPM, constructed based on these indicators, demonstrated good discriminative ability in both the training and validation sets, with AUC values of 0.86(95%CI: 0.82~0.89) and 0.81(95%CI: 0.77~0.85), respectively, which were significantly better than those of FLI [training set: AUC=0.83(95%CI: 0.79~0.87); validation set: AUC=0.74(95%CI: 0.70~0.79)] and HSI [training set: AUC=0.71(95%CI: 0.66~0.76); validation set: AUC=0.71(95%CI: 0.65~0.76)]. Compared with FLI and HSI, the LMPM showed improvements in NRI and IDI in both the training and validation sets. The calibration curve demonstrated its high accuracy, and both the decision curve analysis and the clinical impact curve analysis indicated that the LMPM provided greater clinical benefits. Conclusion‍ ‍Age, waist circumference, and TG are independent risk factors for lean MASLD. Based on these factors, a prediction model, named LMPM, is developed to assess the risk of MASLD in lean individuals, which exhibits good predictive performance and has certain guiding significance for the timely identification of high-risk populations.
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spelling doaj-art-c88c2a4305b04df8a17eb901fda2427b2025-08-20T02:15:28ZzhoEditorial Office of Journal of Army Medical University陆军军医大学学报2097-09272025-05-0147996997910.16016/j.2097-0927.202412024Construction and validation of a risk prediction model for lean metabolic dysfunction-associated steatotic liver diseaseQIN Jiayi0ZHOU Xueqian1MENG Xiangyong2Department of Gastroenterology, First Affiliated Hospital, Army Medical University(Third Military Medical University), Chongqing, ChinaDepartment of Gastroenterology, First Affiliated Hospital, Army Medical University(Third Military Medical University), Chongqing, ChinaDepartment of Gastroenterology, First Affiliated Hospital, Army Medical University(Third Military Medical University), Chongqing, ChinaObjective‍ ‍To investigate the risk factors for the occurrence of metabolic dysfunction-associated steatotic liver disease(MASLD) in lean individuals and construct a risk prediction model. Methods‍ ‍Based on the National Health and Nutrition Examination Survey(NHANES) database in the United States(from January 2017 to March 2020), 1 123 adult individuals were included in this study. Then the participants were randomly divided into a training set(n=561) and a validation set(n=562) through simple random sampling. Data on their demographics, anthropometrics, lifestyle, underlying diseases, and laboratory test results were collected. LASSO regression analysis was used to screen potential variables in the training set, and multivariate logistic regression was employed to identify independent risk factors for lean MASLD. Based on these risk factors, a prediction model for lean MASLD was constructed(LMPM). To evaluate the clinical value of the LMPM, it was compared with two commonly used prediction models for non-alcoholic fatty liver disease, the fatty liver index(FLI) and the hepatic steatosis index(HSI). The performance of the model was evaluated and internally validated using the area under the receiver operating characteristic curve(AUC), net reclassification index(NRI), integrated discrimination improvement(IDI), calibration curve, decision curve, and clinical impact curve. Results‍ ‍Age, waist circumference, and triglycerides(TG) were identified as independent risk factors for the development of MASLD in lean individuals. The LMPM, constructed based on these indicators, demonstrated good discriminative ability in both the training and validation sets, with AUC values of 0.86(95%CI: 0.82~0.89) and 0.81(95%CI: 0.77~0.85), respectively, which were significantly better than those of FLI [training set: AUC=0.83(95%CI: 0.79~0.87); validation set: AUC=0.74(95%CI: 0.70~0.79)] and HSI [training set: AUC=0.71(95%CI: 0.66~0.76); validation set: AUC=0.71(95%CI: 0.65~0.76)]. Compared with FLI and HSI, the LMPM showed improvements in NRI and IDI in both the training and validation sets. The calibration curve demonstrated its high accuracy, and both the decision curve analysis and the clinical impact curve analysis indicated that the LMPM provided greater clinical benefits. Conclusion‍ ‍Age, waist circumference, and TG are independent risk factors for lean MASLD. Based on these factors, a prediction model, named LMPM, is developed to assess the risk of MASLD in lean individuals, which exhibits good predictive performance and has certain guiding significance for the timely identification of high-risk populations. https://aammt.tmmu.edu.cn/html/202412024.html‍lean metabolic dysfunction-associated steatotic liver diseaserisk factorsprediction model
spellingShingle QIN Jiayi
ZHOU Xueqian
MENG Xiangyong
Construction and validation of a risk prediction model for lean metabolic dysfunction-associated steatotic liver disease
陆军军医大学学报
‍lean metabolic dysfunction-associated steatotic liver disease
risk factors
prediction model
title Construction and validation of a risk prediction model for lean metabolic dysfunction-associated steatotic liver disease
title_full Construction and validation of a risk prediction model for lean metabolic dysfunction-associated steatotic liver disease
title_fullStr Construction and validation of a risk prediction model for lean metabolic dysfunction-associated steatotic liver disease
title_full_unstemmed Construction and validation of a risk prediction model for lean metabolic dysfunction-associated steatotic liver disease
title_short Construction and validation of a risk prediction model for lean metabolic dysfunction-associated steatotic liver disease
title_sort construction and validation of a risk prediction model for lean metabolic dysfunction associated steatotic liver disease
topic ‍lean metabolic dysfunction-associated steatotic liver disease
risk factors
prediction model
url https://aammt.tmmu.edu.cn/html/202412024.html
work_keys_str_mv AT qinjiayi constructionandvalidationofariskpredictionmodelforleanmetabolicdysfunctionassociatedsteatoticliverdisease
AT zhouxueqian constructionandvalidationofariskpredictionmodelforleanmetabolicdysfunctionassociatedsteatoticliverdisease
AT mengxiangyong constructionandvalidationofariskpredictionmodelforleanmetabolicdysfunctionassociatedsteatoticliverdisease