Computation of an MRI brain atlas from a population of Parkinson’s disease patients

Zugehörigkeit
Department of Electrical Engineering and Informatics, Cyprus University of Technology ,Limassol ,Cyprus
Angelidakis, L;
GND
1064119417
Zugehörigkeit
Institute of Diagnostic and Interventional Radiology University of Jena ,Jena ,Germany
Papageorgiou, I E;
Zugehörigkeit
Department of Electrical Engineering and Informatics, Cyprus University of Technology ,Limassol ,Cyprus
Damianou, C;
Zugehörigkeit
Department of Diagnostic and Interventional Neuroradiology, University Medical Center Goettingen, University of Goettingen ,Goettingen ,Germany
Psychogios, M N;
Zugehörigkeit
Department of Neurology, University Medical Center Goettingen, University of Goettingen ,Goettingen ,Germany
Lingor, P;
Zugehörigkeit
Department of Neurosurgery, University Medical Center Goettingen, University of Goettingen ,Goettingen ,Germany
von Eckardstein, K;
Zugehörigkeit
Department of Electrical Engineering and Informatics, Cyprus University of Technology ,Limassol ,Cyprus
Hadjidemetriou, S

Abstract Parkinson’s Disease (PD) is a degenerative disorder of the brain. This study presents an MRI-based brain atlas of PD to characterize associated alterations for diagnostic and interventional purposes. The atlas standardizes primarily the implicated subcortical regions such as the globus pallidus (GP), substantia nigra (SN), subthalamic nucleus (STN), caudate nucleus (CN), thalamus (TH), putamen (PUT), and red nucleus (RN). The data were 3.0 T MRI brain images from 16 PD patients and 10 matched controls. The images used were T1-weighted ( T 1 w ), T2-weighted ( T 2 w ) images, and Susceptibility Weighted Images (SWI). The T1w images were the reference for the inter-subject non-rigid registration available from 3DSlicer. Anatomic labeling was achieved with BrainSuite and regions were refined with the level sets segmentation of ITK-Snap. The subcortical centers were analyzed for their volume and signal intensity. Comparison with an age-matched control group unravels a significant PD-related T1w signal loss in the striatum (CN and PUT) centers, but approximately a constant volume. The results in this study improve MRI based PD localization and can lead to the development of novel biomarkers.

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