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NeuroImageNeurosciencePeer-reviewed journal article

DeepQSM - Using Deep Learning to Solve the Dipole Inversion for MRI Susceptibility Mapping

Steffen BollmanniD, Kasper Gade Bøtker-Rasmussen, Mads Kristensen, Rasmus Guldhammer Blendal, Lasse Riis ØstergaardiD, Maciej PlocharskiiD, Kieran O’BrieniD, Christian LangkammeriD, Andrew L. JankeiD, Markus BarthiD

PDFDOIPreprint

Abstract

Quantitative susceptibility mapping (QSM) aims to extract the magnetic susceptibility of tissue from magnetic resonance imaging (MRI) phase measurements. The mapping of magnetic susceptibility in vivo has gained broad interest in several fields of science and medicine because it yields relevant information on biological tissue properties, predominantly myelin, iron and calcium. Thereby, QSM can also reveal pathological changes of these key components in devastating diseases such as Parkinsons disease, Multiple Sclerosis, or hepatic iron overload. As QSM requires the solution of an ill-posed field-to-source-inversion, current techniques utilize manual optimization of regularization parameters to balance between smoothing, artifacts and quantification accuracy. We trained a fully convolutional deep neural network - DeepQSM - to invert the magnetic dipole kernel convolution. This network is capable of solving the ill-posed field-to-source inversion on real-world in vivo MRI phase data without the need for manual parameter tuning, which proves that this network has generalized the underlying mathematical principle of the dipole inversion. We demonstrate that DeepQSMs susceptibility maps enable identification of deep brain substructures that are not visible in MRI phase data and provide information on their respective magnetic tissue properties. We illustrate DeepQSMs clinical relevance in a patient with multiple sclerosis showing its sensitivity to white matter lesions. In summary, DeepQSM can be used to determine the composition of myelin sheets of nerve fibers in the brain, and to assess quantitative information on iron homeostasis and its dysregulation, and will subsequently contribute to a better understanding of these biological processes in health and disease.

Citations
132
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