Functional MRI for the early detection of Parkinson’s disease: ROI analysis of the putamen in a population at risk of developing Parkinson’s disease

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URI: http://hdl.handle.net/10900/127022
http://nbn-resolving.de/urn:nbn:de:bsz:21-dspace-1270220
http://dx.doi.org/10.15496/publikation-68385
Dokumentart: Dissertation
Date: 2022-05-12
Language: English
Faculty: 4 Medizinische Fakultät
Department: Medizin
Advisor: Berg, Daniela (Prof. Dr.)
Day of Oral Examination: 2021-08-26
DDC Classifikation: 610 - Medicine and health
Other Keywords:
neurology
parkinson
fMRI
prodromal
putamen
License: Publishing license including print on demand
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Inhaltszusammenfassung:

Background: While the concept of prodromal Parkinson’s disease (PD) is well established, reliable markers for the diagnosis of this disease stage are still lacking. We investigated the functional connectivity of the putamina in a resting-state functional MRI analysis in persons with at least two prodromal factors for PD, which is considered a high risk for PD (HRPD) group, in comparison to PD patients and controls. Methods: We included 16 PD patients, 20 healthy controls and 20 HRPD subjects. Resting state echo planar images and anatomical T1-weighted images were acquired with a Siemens Prisma 3 Tesla scanner. The computation of correlation maps of the left and the right puta-men to the rest of the brain was done in a voxel-wise approach using the REST toolbox. Finally, group differences in the correlation maps were compared on voxel-level and summarized in cluster z-statistics. Results: Compared to both PD patients and healthy controls, the HRPD group showed higher functional connectivity of both putamina to brain regions involved in execution of motion and coordination (cerebellum, vermis, pre- and postcentral gyrus, supplementary motor area) as well as the planning of movement (precuneus, cuneus, superior medial frontal lobe). Conclusions: Higher functional connectivity of the putamina of HRPD subjects to other brain regions involved in motor execution and planning may indicate a compensatory mechanism. Follow-up evaluation and independent longitudinal studies should test whether our results re-flect a dynamic process associated with a prodromal PD state.

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