• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基于机器学习的肝纤维化和MASH预测模型的开发与验证

Development and Validation of a Machine Learning-based Model for Prediction of Liver Fibrosis and MASH.

作者信息

Liu Maojie, Jiang Longfeng, Yang Juan, Yao Yao, Puyang Xuerong, Ge Xinyuan, Lu Jing, Zhang Lu, Yan Yuqian, Shen Hongbing, Song Ci

机构信息

Department of Epidemiology.

Departments of Infectious Disease.

出版信息

J Clin Gastroenterol. 2025 Apr 25. doi: 10.1097/MCG.0000000000002166.

DOI:10.1097/MCG.0000000000002166
PMID:40299904
Abstract

BACKGROUND AND AIM

The development of accurate noninvasive tests to identify individuals with metabolic dysfunction-associated steatohepatitis (MASH) and liver fibrosis is of great clinical importance. In this study, we aimed to develop 2 noninvasive diagnostic models on the basis of routine clinical and laboratory data, using machine learning, to identify patients with MASH and significant fibrosis (fibrosis stages 2 to 4), respectively.

METHODS

This analysis included the training (n=456) and the validation (n=105) sets of patients who underwent liver biopsy and laboratory testing for liver disease at 2 hospitals in China. Logistic regression, random forest, support vector machine, and the XGBoost algorithm were used to construct models, respectively. The best diagnostic models for MASH and significant fibrosis were compared with 7 existing noninvasive scoring systems including AAR, AST to platelet ratio index (APRI), BARD score, fibrosis-4 (FIB-4), fibrotic non-alcoholic steatohepatitis (NASH) index (FNI), homeostatic model assessment of insulin resistance (HOMA-IR), and non-alcoholic fatty liver disease fibrosis score (NFS). Performance was estimated by the area under the receiver operating characteristic curve (AUROC).

RESULTS

The final noninvasive diagnostic model integrated 19 indicators derived from routine clinical and laboratory tests. The XGBoost models exhibited superior performance in MASH and significant fibrosis with an improved AUROC value (MASH, 0.670, 95% CI 0.530-0.811; significant fibrosis, 0.713, 95% CI 0.611-0.815) compared with other noninvasive scoring systems in the validation set.

CONCLUSIONS

Utilizing machine learning can assist in diagnosing MASH and significant fibrosis based on clinical epidemiological information with good diagnostic performance.

摘要

背景与目的

开发准确的非侵入性检测方法以识别代谢功能障碍相关脂肪性肝炎(MASH)和肝纤维化患者具有重要的临床意义。在本研究中,我们旨在基于常规临床和实验室数据,利用机器学习分别开发2种非侵入性诊断模型,以识别MASH患者和显著纤维化(纤维化2至4期)患者。

方法

该分析纳入了在中国2家医院接受肝活检及肝病实验室检测的患者的训练集(n = 456)和验证集(n = 105)。分别使用逻辑回归、随机森林、支持向量机和XGBoost算法构建模型。将MASH和显著纤维化的最佳诊断模型与7种现有的非侵入性评分系统进行比较,包括天冬氨酸氨基转移酶与碱性磷酸酶比值(AAR)、天冬氨酸氨基转移酶与血小板比值指数(APRI)、BARD评分、纤维化-4(FIB-4)、纤维化非酒精性脂肪性肝炎(NASH)指数(FNI)、胰岛素抵抗稳态模型评估(HOMA-IR)和非酒精性脂肪性肝病纤维化评分(NFS)。通过受试者操作特征曲线下面积(AUROC)评估性能。

结果

最终的非侵入性诊断模型整合了19个源自常规临床和实验室检测的指标。在验证集中,与其他非侵入性评分系统相比,XGBoost模型在MASH和显著纤维化方面表现出更优性能,AUROC值有所提高(MASH为0.670,95%CI为0.530 - 0.811;显著纤维化为0.713,95%CI为0.611 - 0.815)。

结论

利用机器学习可基于临床流行病学信息辅助诊断MASH和显著纤维化,诊断性能良好。

相似文献

1
Development and Validation of a Machine Learning-based Model for Prediction of Liver Fibrosis and MASH.基于机器学习的肝纤维化和MASH预测模型的开发与验证
J Clin Gastroenterol. 2025 Apr 25. doi: 10.1097/MCG.0000000000002166.
2
Noninvasive identification of metabolic dysfunction-associated steatohepatitis (INFORM MASH): a retrospective cohort and disease modeling study.代谢功能障碍相关脂肪性肝炎的非侵入性识别(INFORM MASH):一项回顾性队列和疾病建模研究。
Expert Rev Gastroenterol Hepatol. 2025 Apr;19(4):427-435. doi: 10.1080/17474124.2025.2477249. Epub 2025 Mar 21.
3
Diagnostic Accuracy of Noninvasive Scores for Fibrotic MASH in a Cohort of Biopsy-proven MASLD Patients With Predominantly High BMI in the Primary Care Setting.在基层医疗环境中,对一组经活检证实、BMI主要偏高的MASLD患者,非侵入性评分对纤维化MASH的诊断准确性。
J Clin Exp Hepatol. 2025 Sep-Oct;15(5):102556. doi: 10.1016/j.jceh.2025.102556. Epub 2025 Mar 25.
4
FibroScan-aspartate transaminase: A superior non-invasive model for diagnosing high-risk metabolic dysfunction-associated steatohepatitis.纤维扫描天门冬氨酸转氨酶:诊断高危代谢功能障碍相关脂肪性肝炎的一种更优的非侵入性模型。
World J Gastroenterol. 2024 May 14;30(18):2440-2453. doi: 10.3748/wjg.v30.i18.2440.
5
Noninvasive fibrosis tools in NAFLD: validation of APRI, BARD, FIB-4, NAFLD fibrosis score, and Hepamet fibrosis score in a Portuguese population.非酒精性脂肪性肝病无创性纤维化工具:APRI、BARD、FIB-4、NAFLD 纤维化评分和 Hepamet 纤维化评分在葡萄牙人群中的验证。
Postgrad Med. 2022 May;134(4):435-440. doi: 10.1080/00325481.2022.2058285. Epub 2022 Mar 30.
6
Machine learning-based models for advanced fibrosis in non-alcoholic steatohepatitis patients: A cohort study.基于机器学习的非酒精性脂肪性肝炎患者晚期纤维化模型:一项队列研究。
World J Gastroenterol. 2025 Mar 7;31(9):101383. doi: 10.3748/wjg.v31.i9.101383.
7
Development and validation of an ensemble machine learning framework for detection of all-cause advanced hepatic fibrosis: a retrospective cohort study.用于检测全因性晚期肝纤维化的集成机器学习框架的开发与验证:一项回顾性队列研究
Lancet Digit Health. 2022 Mar;4(3):e188-e199. doi: 10.1016/S2589-7500(21)00270-3.
8
Accurate non-invasive detection of MASH with fibrosis F2-F3 using a lightweight machine learning model with minimal clinical and metabolomic variables.使用具有最少临床和代谢组学变量的轻量级机器学习模型对伴有F2-F3纤维化的MASH进行准确的非侵入性检测。
Metabolism. 2025 Feb;163:156082. doi: 10.1016/j.metabol.2024.156082. Epub 2024 Nov 19.
9
A metabolome-derived score predicts metabolic dysfunction-associated steatohepatitis and mortality from liver disease.代谢组衍生评分可预测代谢功能障碍相关脂肪性肝炎及肝病死亡率。
J Hepatol. 2025 May;82(5):781-793. doi: 10.1016/j.jhep.2024.10.015. Epub 2024 Oct 16.
10
Development and Validation of Hepamet Fibrosis Scoring System-A Simple, Noninvasive Test to Identify Patients With Nonalcoholic Fatty Liver Disease With Advanced Fibrosis.Hepamet纤维化评分系统的开发与验证——一种用于识别非酒精性脂肪性肝病伴晚期纤维化患者的简单无创检测方法
Clin Gastroenterol Hepatol. 2020 Jan;18(1):216-225.e5. doi: 10.1016/j.cgh.2019.05.051. Epub 2019 Jun 11.