LASSO 衍生模型用于预测参加例行健康检查的受检者是否患有 "瘦-非酒精性脂肪肝"。

Annals of medicine Pub Date : 2024-12-01 Epub Date: 2024-02-16 DOI:10.1080/07853890.2024.2317348
Chiao-Lin Hsu, Pin-Chieh Wu, Fu-Zong Wu, Hsien-Chung Yu
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引用次数: 0

摘要

背景:患有非酒精性脂肪肝(NAFLD)的瘦人通常体型正常,但内脏脂肪异常。因此,在预测非酒精性脂肪肝时应考虑体重指数以外的其他方法。本研究旨在使用最小绝对收缩和选择算子(LASSO)方法,将具有代表性的内脏脂肪与其他实验室参数联系起来,构建瘦-非酒精性脂肪肝的预测模型:这项回顾性横断面分析从 51271 名接受常规健康检查的受检者的医疗记录中选取了 2325 名体重指数小于 24 kg/m2 的受检者。他们按 1:1 的比例被随机分为训练组和验证组。LASSO 衍生预测模型使用 LASSO 回归法选择 23 个临床和实验室因素。使用 Hosmer-Lemeshow 检验和校准曲线评估了模型的判别和校准能力。将 LASSO 模型的性能与脂肪肝指数(FLI)模型进行了比较:LASSO衍生模型包括四个变量--内脏脂肪、甘油三酯水平、HDL-C-C水平和腰臀比,在预测瘦-NAFLD方面表现优异,具有较高的判别能力(AUC,0.8416;95% CI:0.811-0.872),与FLI模型相当。以 0.1484 为临界值,LASSO 模型达到了中等灵敏度(75.69%)和特异性(79.86%)以及较高的阴性预测值(95.9%)。此外,在对正常 WC 进行亚组分析时,LASSO 模型与 FLI(临界值为 15.45)相比呈现出更高的准确性趋势:结论:我们开发了一个 LASSO 衍生预测模型,该模型有望在临床环境中用作预测瘦-NAFLD 的替代工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
LASSO-derived model for the prediction of lean-non-alcoholic fatty liver disease in examinees attending a routine health check-up.

Background: Lean individuals with non-alcohol fatty liver disease (NAFLD) often have normal body size but abnormal visceral fat. Therefore, an alternative to body mass index should be considered for prediction of lean-NAFLD. This study aimed to use representative visceral fat links with other laboratory parameters using the least absolute shrinkage and selection operator (LASSO) method to construct a predictive model for lean-NAFLD.

Methods: This retrospective cross-sectional analysis enrolled 2325 subjects with BMI < 24 kg/m2 from medical records of 51,271 examinees who underwent a routine health check-up. They were randomly divided into training and validation cohorts at a ratio of 1:1. The LASSO-derived prediction model used LASSO regression to select 23 clinical and laboratory factors. The discrimination and calibration abilities were evaluated using the Hosmer-Lemeshow test and calibration curves. The performance of the LASSO model was compared with the fatty liver index (FLI) model.

Results: The LASSO-derived model included four variables-visceral fat, triglyceride levels, HDL-C-C levels, and waist hip ratio-and demonstrated superior performance in predicting lean-NAFLD with high discriminatory ability (AUC, 0.8416; 95% CI: 0.811-0.872) that was comparable with the FLI model. Using a cut-off of 0.1484, moderate sensitivity (75.69%) and specificity (79.86%), as well as high negative predictive value (95.9%), were achieved in the LASSO model. In addition, with normal WC subgroup analysis, the LASSO model exhibits a trend of higher accuracy compared to FLI (cut-off 15.45).

Conclusions: We developed a LASSO-derived predictive model with the potential for use as an alternative tool for predicting lean-NAFLD in clinical settings.

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