Automatic Lesion Segmentation on MRI Scans of Patients with Multiple Sclerosis

PhD Project by Amalie Hindsholm

Introduction

The purpose of the project is to improve Multiple sclerosis (MS) lesion segmentation accuracy by utilizing large, heterogeneous clinical datasets and Deep Learning technology. These large-scale datasets from clinical practice are used to develop decision-support models for radiologists in the context of MS, specifically for the segmentation of MS lesion on magnetic resonance imaging (MRI). The objective is the clinical deployment of this model, which requires high-performance and adaptability to new scanners.

Project Background

MS is a chronic autoimmune disease of the central nervous system (CNS), causing long-term functional impairment. The disease is characterized by inflammatory axonal demyelination, resulting in focal lesions in the grey and white matter of the CNS, which serve as important biomarkers for disease diagnosis, activity, and treatment response. As part of their disease management, patients routinely undergo repeated MRI scans, contributing to a considerable workload for radiologists.
While there are existing models for automatic lesion segmentation, only a few are currently utilized in clinical practice. The existing models are struggling with generalization to clinical datasets. This is where this project steps in by incorporating large, heterogeneous training datasets directly from the MS clinics for training and validating an MS lesion segmentation model. The outcome is a model that achieves high precision and robustness against data from scanners that were not previously encountered.

Project Potential

The project enables the practical use of MS lesion segmentation in clinics, enabling the model to handle the variation found in clinical practice. This has the potential to reduce the time spent reviewing routine MS MRI scans for radiologists in the clinic and enable quantification of lesion volume as a biomarker.

Figure 1: MRI images from seven patients, - from seven different scanners. Two delineations: lesions marked by segmentation model (blue), and a reference delineation marked by a radiologist (pink).

Contact Information

Name: Amalie Monberg Hindsholm
Location: Department of Clinical Physiology and Nuclear Medicine, 3982
Position: PhD Student

Publications