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MRI-based interpretable deep learning radiomics for predicting treatment response in axial spondyloarthritis.

May 1, 2026pubmed logopapers

Authors

Xie Z,Lu K,Liu Y,Chen D,Qiu Z,Yang Q,Ye Q,Zheng K,Li S,Zhang R,He Y,Han X,Chen Y,Yu L,Zhao Y

Affiliations (15)

  • Department of Radiology, The Third Affiliated Hospital of Southern Medical University, Guangzhou, China; Institute of High-End Intelligent Health Equipment, Academy of Orthopedics, Guangdong Province, The Third Affiliated Hospital of Southern Medical University, Guangzhou, China. Electronic address: [email protected].
  • School of Computing and Data Science, The University of Hong Kong, Hong Kong SAR, China. Electronic address: [email protected].
  • Department of Radiology, The Third Affiliated Hospital of Southern Medical University, Guangzhou, China; Institute of High-End Intelligent Health Equipment, Academy of Orthopedics, Guangdong Province, The Third Affiliated Hospital of Southern Medical University, Guangzhou, China. Electronic address: [email protected].
  • Department of Radiology, The Third Affiliated Hospital of Southern Medical University, Guangzhou, China; Institute of High-End Intelligent Health Equipment, Academy of Orthopedics, Guangdong Province, The Third Affiliated Hospital of Southern Medical University, Guangzhou, China. Electronic address: [email protected].
  • Department of Computer Science and Engineering, The Hong Kong University of Science and Technology, Hong Kong SAR, China. Electronic address: [email protected].
  • Department of Radiology, The Third Affiliated Hospital of Southern Medical University, Guangzhou, China. Electronic address: [email protected].
  • Department of Radiology, The Third Affiliated Hospital of Southern Medical University, Guangzhou, China. Electronic address: [email protected].
  • Department of Radiology, The Third Affiliated Hospital of Zunyi Medical University, Zunyi, China. Electronic address: [email protected].
  • Department of Radiology, The Third Affiliated Hospital of Southern Medical University, Guangzhou, China. Electronic address: [email protected].
  • Department of Radiology, The Third Affiliated Hospital of Southern Medical University, Guangzhou, China. Electronic address: [email protected].
  • Department of Rheumatology and Immunology, The Third Affiliated Hospital of Southern Medical University, Guangzhou, China. Electronic address: [email protected].
  • Department of Rheumatology and Immunology, The Third Affiliated Hospital of Southern Medical University, Guangzhou, China. Electronic address: [email protected].
  • Department of Radiology, The Third Affiliated Hospital of Southern Medical University, Guangzhou, China. Electronic address: [email protected].
  • School of Computing and Data Science, The University of Hong Kong, Hong Kong SAR, China. Electronic address: [email protected].
  • Department of Radiology, The Third Affiliated Hospital of Southern Medical University, Guangzhou, China; Institute of High-End Intelligent Health Equipment, Academy of Orthopedics, Guangdong Province, The Third Affiliated Hospital of Southern Medical University, Guangzhou, China. Electronic address: [email protected].

Abstract

The clinical efficacy of tumor necrosis factor inhibitors (TNFi) in axial spondyloarthritis (axSpA) is limited by high non-response rates, necessitating accurate pre-treatment stratification. This study aimed to develop and validate MRI-based interpretable deep learning radiomics (DLR) models to predict treatment response to TNFi in patients with axSpA. In this prospective study, patients diagnosed with axSpA who underwent sacroiliac joint MRI before TNFi initiation were enrolled. Patients were allocated to training and test sets at an approximate 4:1 ratio. The endpoints were major (ASAS40) and moderate (ASAS20) improvement, as defined by the Assessment of SpondyloArthritis International Society criteria. Deep learning and radiomics features were extracted from MRI. A four-step selection process, including reproducibility analysis, univariable filtering, redundancy reduction, and LASSO regression, was used to distill robust predictors. These were then integrated with clinical data to build DLR-clinical (DLRC) models using L2-regularized logistic regression. A total of 183 patients (mean age, 26.5 ± 9.0 years; 121 [66.1%] males) were analyzed. The DLRC models were validated on the independent test set, with high area under the receiver operating characteristic curve (AUC) values for predicting ASAS40 (0.876, 95%CI: 0.738-0.973) and ASAS20 (0.886, 95%CI: 0.753-0.978) responses. Calibration curves indicated good model agreement, and decision curve analysis (DCA) confirmed their clinical utility. Compared to the clinical-only model, the DLRC models showed significant integrated discrimination improvement (IDI) for ASAS40 and ASAS20 (0.234 and 0.283, all p < 0.05) prediction, respectively. MRI-based interpretable DLR models accurately predicted TNFi treatment response in axSpA patients, offering a non-invasive tool to guide personalized therapy.

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