Identifying Nonalcoholic Fatty Liver Disease and Advanced Liver Fibrosis from MRI in UK Biobank

被引:0
作者
Al-Belmpeisi, Rami [1 ,3 ]
Sorensen, Kristine Aavild [1 ,3 ]
Sundgaard, Josefine Vilsbo [1 ,3 ]
Nabilou, Puria [2 ,4 ]
Emerson, Monica Jane [3 ]
Larsen, Peter Hjorringgaard [3 ]
Gluud, Lise Lotte [2 ,5 ]
Andersen, Thomas Lund [2 ,4 ]
Dahl, Anders Bjorholm [1 ]
机构
[1] Tech Univ Denmark, Dept Appl Math & Comp Sci, Lyngby, Denmark
[2] Copenhagen Univ Hosp Hvidovre, Gastro Unit, Hvidovre, Denmark
[3] Novo Nordisk, Copenhagen, Denmark
[4] Univ Copenhagen, Rigshosp, Dept Clin Physiol & Nucl Med, Copenhagen, Denmark
[5] Univ Copenhagen, Fac Hlth & Med Sci, Dept Clin Med, Copenhagen, Denmark
来源
MACHINE LEARNING IN MEDICAL IMAGING, PT II, MLMI 2024 | 2025年 / 15242卷
关键词
Non-alcoholic fatty liver disease; Non-alcoholic steatohepatitis; Liver biopsy; Magnetic resonance imaging; Proton density fat fraction; Native spin-latice relaxation time; Serum biomarkers; Advanced Fibrosis; UK Biobank; Imaging biomarkers; PREVALENCE;
D O I
10.1007/978-3-031-73290-4_22
中图分类号
TP18 [人工智能理论];
学科分类号
081104 ; 0812 ; 0835 ; 1405 ;
摘要
Non-alcoholic fatty liver disease (NAFLD) and its progressive form of non-alcoholic steatohepatitis (NASH) pose a major public health problem that affects more than 30% of the global population. Since NAFLD is asymptomatic in the early stages, sufferers often remain untreated until the onset of NASH, which can lead to fibrosis and eventually cirrhosis of the liver. This condition is traditionally diagnosed via liver biopsy, which is invasive and associated with significant risks for the patient and susceptibility to sampling errors. These limitations underscore the necessity for non-invasive tools to assess disease severity. We explore the potential of magnetic resonance imaging (MRI) sequences in the UK Biobank (UKBB) to classify individuals as having either a healthy liver, NAFLD, or progressive NAFLD-associated advanced fibrosis. For the classification inputs, we utilize proton density fat fraction (PDFF) and native spin-lattice relaxation time (T1) maps, as well as serum biomarker data for assessing the sub-cohorts. The best models achieve near-perfect performance on identifying healthy individuals and NAFLD with AUCs of 0.99 and 0.98 respectively, while individuals with advanced fibrosis are under-diagnosed with an AUC of 0.67 at best. While segmentation decreases model performance, when classifying on full images, we make use of non-liver-related features, which is sub-optimal if we want to detect liver-related imaging biomarkers.
引用
收藏
页码:222 / 231
页数:10
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