IVAICVTONov 25, 2025

LAYER: A Quantitative Explainable AI Framework for Decoding Tissue-Layer Drivers of Myofascial Low Back Pain

arXiv:2511.21767v1
Originality Highly original
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This work addresses the need for better diagnostic tools in chronic low back pain by providing a quantitative, interpretable framework that could influence therapy methods, though it is domain-specific to medical imaging and pain research.

The researchers tackled the problem of identifying tissue-level drivers of myofascial low back pain, which lacks reliable biomarkers, by developing the LAYER explainable AI framework to analyze six tissue layers in 3D ultrasound scans; they found that non-muscle tissues, such as the deep fascial membrane with a saliency of 0.420, contribute substantially to pain prediction, challenging the muscle-centric paradigm.

Myofascial pain (MP) is a leading cause of chronic low back pain, yet its tissue-level drivers remain poorly defined and lack reliable image biomarkers. Existing studies focus predominantly on muscle while neglecting fascia, fat, and other soft tissues that play integral biomechanical roles. We developed an anatomically grounded explainable artificial intelligence (AI) framework, LAYER (Layer-wise Analysis for Yielding Explainable Relevance Tissue), that analyses six tissue layers in three-dimensional (3D) ultrasound and quantifies their contribution to MP prediction. By utilizing the largest multi-model 3D ultrasound cohort consisting of over 4,000 scans, LAYER reveals that non-muscle tissues contribute substantially to pain prediction. In B-mode imaging, the deep fascial membrane (DFM) showed the highest saliency (0.420), while in combined B-mode and shear-wave images, the collective saliency of non-muscle layers (0.316) nearly matches that of muscle (0.317), challenging the conventional muscle-centric paradigm in MP research and potentially affecting the therapy methods. LAYER establishes a quantitative, interpretable framework for linking layer-specific anatomy to pain physiology, uncovering new tissue targets and providing a generalizable approach for explainable analysis of soft-tissue imaging.

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