Comparison of 3T and 7T MRI for the visualization of globus pallidus sub-segments
Autor: | Masaki Fukunaga, Hans-Peter Fautz, Norihiro Sadato, Robin M. Heidemann, Shuki Maruyama |
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Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
Medial medullary lamina
Lamina Multidisciplinary Internal globus pallidus High signal intensity business.industry Parkinson's disease lcsh:R Brain lcsh:Medicine Biology Article 030218 nuclear medicine & medical imaging 03 medical and health sciences 0302 clinical medicine Globus pallidus Text mining lcsh:Q Signal intensity Nuclear medicine business lcsh:Science 030217 neurology & neurosurgery |
Zdroj: | Scientific Reports, Vol 9, Iss 1, Pp 1-8 (2019) Scientific Reports |
ISSN: | 2045-2322 |
DOI: | 10.1038/s41598-019-54880-x |
Popis: | The success of deep brain stimulation (DBS) targeting the internal globus pallidus (GPi) depends on the accuracy of electrode localization inside the GPi. In this study, we sought to compare visualization of the medial medullary lamina (MML) and accessory medullary lamina (AML) between proton density-weighted (PDW) and T2-weighted (T2W) sequences on 3T and 7T MRI scanners. Eleven healthy participants (five men and six women; age, 19–28 years; mean, 21.5) and one 61-year-old man were scanned using two-dimensional turbo spin-echo PDW and T2W sequences on 3T and 7T MRI scanners with a 32-channel receiver head coil and a single-channel transmission coil. Profiles of signal intensity were obtained from the pixel values of straight lines over the GP regions crossing the MML and AML. Contrast ratios (CRs) for GPe/MML, GPie/MML, GPie/AML, and GPii/AML were calculated. Qualitatively, 7T visualized both the MML and AML, whereas 3T visualized the MML less clearly and hardly depicted the AML. The T2W sequence at 7T yielded significantly higher CRs for GPie/MML, GPie/AML, and GPii/AML than the PDW sequence at 7T or 3T. The T2W sequence at 7T allows visualization of the internal structures of GPi segments with high signal intensity and contrast. |
Databáze: | OpenAIRE |
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