Modeling and Reversing Brain Lesions Using Diffusion Models

TL;DR

This paper introduces a diffusion model-based framework for analyzing, reversing, and inpainting brain lesions in MRI images, improving lesion segmentation and characterization by modeling lesion growth and tissue deformation.

Contribution

The novel framework combines lesion segmentation, tissue deformation reversal, and inpainting to estimate pre-lesion healthy brains, addressing limitations of existing methods.

Findings

Enhanced accuracy in lesion segmentation and characterization

Effective reversal of tissue deformation in brain images

Simulation of lesion growth models for validation

Abstract

Brain lesions are abnormalities or injuries in brain tissue that are often detectable using magnetic resonance imaging (MRI), which reveals structural changes in the affected areas. This broad definition of brain lesions includes areas of the brain that are irreversibly damaged, as well as areas of brain tissue that are deformed as a result of lesion growth or swelling. Despite the importance of differentiating between damaged and deformed tissue, existing lesion segmentation methods overlook this distinction, labeling both of them as a single anomaly. In this work, we introduce a diffusion model-based framework for analyzing and reversing the brain lesion process. Our pipeline first segments abnormal regions in the brain, then estimates and reverses tissue deformations by restoring displaced tissue to its original position, isolating the core lesion area representing the initial damage. Finally, we inpaint the core lesion area to arrive at an estimation of the pre-lesion healthy brain. This proposed framework reverses a forward lesion growth process model that is well-established in biomechanical studies that model brain lesions. Our results demonstrate improved accuracy in lesion segmentation, characterization, and brain labeling compared to traditional methods, offering a robust tool for clinical and research applications in brain lesion analysis. Since pre-lesion healthy versions of abnormal brains are not available in any public dataset for validation of the reverse process, we simulate a forward model to synthesize multiple lesioned brain images.