Development and validation of an online dynamic nomogram for nonobese metabolic dysfunction-associated steatotic liver disease based on body composition analysis.

IF 3.2 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Tingting Zheng, Haizhen Yang, Sijia Wang, Xiaoqin Shi, Qingxiu Zhang, Zhongmin Wen
{"title":"Development and validation of an online dynamic nomogram for nonobese metabolic dysfunction-associated steatotic liver disease based on body composition analysis.","authors":"Tingting Zheng, Haizhen Yang, Sijia Wang, Xiaoqin Shi, Qingxiu Zhang, Zhongmin Wen","doi":"10.1186/s12876-026-04972-6","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>The factors influencing nonobese Metabolic dysfunction-associated steatotic liver disease are discussed, and an online dynamic nomogram model is constructed.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusion: </strong>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.</p>","PeriodicalId":9129,"journal":{"name":"BMC Gastroenterology","volume":" ","pages":""},"PeriodicalIF":3.2000,"publicationDate":"2026-07-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13656371/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Gastroenterology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s12876-026-04972-6","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GASTROENTEROLOGY & HEPATOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

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.

基于身体成分分析的非肥胖代谢功能障碍相关脂肪变性肝病在线动态图的开发和验证。
背景:讨论非肥胖代谢功能障碍相关脂肪变性肝病的影响因素,并构建在线动态图模型。方法:回顾性分析苏州大学第二附属医院非肥胖MASLD患者216例及非肥胖健康对照322例的临床资料。数据按7:3的比例随机分为训练集和验证集。初步通过单因素分析、相关分析和LASSO回归(包括交叉验证)筛选潜在变量。随后,采用二元logistic回归和SHAP方法识别独立危险因素,构建在线动态ROC曲线。使用曲线下面积(AUC)、灵敏度、特异性、校准曲线和重新校准方法评估模型性能。结果:LASSO回归初步筛选出11个潜在变量。二元logistic回归最终确定了6个独立危险因素:既往病史(比值比(OR): 2.399, P = 0.0008)、甘油三酯(OR: 1.176, P = 0.008)、高密度脂蛋白胆固醇(HDL-C) (OR: 0.173, P = 0.014)、低密度脂蛋白胆固醇(LDL-C) (OR: 3.916, P = 0.001)、脂肪量(OR: 4.299, P = 0.0009)和dPhaseAngle(OR: 3.174, P = 0.022)。SHAP分析显示TG是影响最大的特征,而HDL-C呈负贡献。所有方差膨胀因子(VIF)值均小于1.5,说明没有显著的多重共线性。训练组的AUC为0.869,验证组的AUC为0.802。标定曲线表明,该结果的线形图预测结果与理想曲线非常接近,与实际结果一致。结论:构建了识别性能良好的非肥胖MASLD患者在线动态图,可作为个性化早期筛查和潜在危险因素辅助诊断的实用手段,可协助医生对患者进行个性化诊断和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
BMC Gastroenterology
BMC Gastroenterology 医学-胃肠肝病学
CiteScore
4.20
自引率
0.00%
发文量
465
审稿时长
6 months
期刊介绍: BMC Gastroenterology is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of gastrointestinal and hepatobiliary disorders, as well as related molecular genetics, pathophysiology, and epidemiology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书