为膝关节MRI开发可解释的个性化特征指纹与健康基准模型
Interpretability and Individuality in Knee MRI: Patient-Specific Radiomic Fingerprint with Reconstructed Healthy Personas
- 动态构建患者特异性影像组学特征集,按需选择最相关特征
- 在三类临床任务中性能媲美甚至超过主流深度学习模型
- 适合需要可解释性诊断的临床研究与医生辅助决策场景
自动化评估膝关节MRI需兼顾准确性和可解释性。传统影像组学依赖群体层面预设特征,虽可解释但难以捕捉个体差异且性能常落后于端到端深度学习。为此,本文提出互补策略:一是构建患者特异性影像组学指纹,从候选特征池中根据图像条件预测特征重要性,仅保留对个体最相关的特征,结合透明逻辑回归实现分类;二是利用扩散模型生成每位患者的病理无病基准(健康人格),通过对比病灶图像与健康人格的特征差异,直观揭示病变位置与程度。在三个临床任务中系统评估发现,两种方法性能均达或超越当前最优深度学习模型,同时支持多层次可解释性。案例研究进一步表明其有助于人类可理解的生物标志物发现与病理定位。
原文摘要 · Abstract (English)
For automated assessment of knee MRI scans, both accuracy and interpretability are essential for clinical use and adoption. Traditional radiomics rely on predefined features chosen at the population level; while more interpretable, they are often too restrictive to capture patient-specific variability and can underperform end-to-end deep learning (DL). To address this, we propose two complementary strategies that bring individuality and interpretability: radiomic fingerprints and healthy personas. First, a radiomic fingerprint is a dynamically constructed, patient-specific feature set derived from MRI. Instead of applying a uniform population-level signature, our model predicts feature relevance from a pool of candidate features and selects only those most predictive for each patient, while maintaining feature-level interpretability. This fingerprint can be viewed as a latent-variable model of feature usage, where an image-conditioned predictor estimates usage probabilities and a transparent logistic regression with global coefficients performs classification. Second, a healthy persona synthesises a pathology-free baseline for each patient using a diffusion model trained to reconstruct healthy knee MRIs. Comparing features extracted from pathological images against their personas highlights deviations from normal anatomy, enabling intuitive, case-specific explanations of disease manifestations. We systematically compare fingerprints, personas, and their combination across three clinical tasks. Experimental results show that both approaches yield performance comparable to or surpassing state-of-the-art DL models, while supporting interpretability at multiple levels. Case studies further illustrate how these perspectives facilitate human-explainable biomarker discovery and pathology localisation.
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