Quantitative Susceptibility Mapping of the Basal Ganglia and Thalamus at 9.4 Tesla
The thalamus (Th) and basal ganglia (BG) are central subcortical connectivity hubs of the human brain, whose functional anatomy is still under intense investigation. Nevertheless, both substructures contain a robust and reproducible functional anatomy. The quantitative susceptibility mapping (QSM) a...
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Published in | Frontiers in neuroanatomy Vol. 15; p. 725731 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Lausanne
Frontiers Research Foundation
16.09.2021
Frontiers Media S.A |
Subjects | |
Online Access | Get full text |
ISSN | 1662-5129 1662-5129 |
DOI | 10.3389/fnana.2021.725731 |
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Summary: | The thalamus (Th) and basal ganglia (BG) are central subcortical connectivity hubs of the human brain, whose functional anatomy is still under intense investigation. Nevertheless, both substructures contain a robust and reproducible functional anatomy. The quantitative susceptibility mapping (QSM) at ultra-high field may facilitate an improved characterization of the underlying functional anatomy
in vivo
. We acquired high-resolution QSM data at 9.4 Tesla in 21 subjects, and analyzed the thalamic and BG by using a prior defined functional parcellation. We found a more substantial contribution of paramagnetic susceptibility sources such as iron in the pallidum in contrast to the caudate, putamen, and Th in descending order. The diamagnetic susceptibility sources such as myelin and calcium revealed significant contributions in the Th parcels compared with the BG. This study presents a detailed nuclei-specific delineation of QSM-provided diamagnetic and paramagnetic susceptibility sources pronounced in the BG and the Th. We also found a reasonable interindividual variability as well as slight hemispheric differences. The results presented here contribute to the microstructural knowledge of the Th and the BG. In specific, the study illustrates QSM values (myelin, calcium, and iron) in functionally similar subregions of the Th and the BG. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Edited by: Jared Brent Smith, Regenxbio Inc., United States Reviewed by: James Mac Shine, The University of Sydney, Australia; Birte U. Forstmann, Max Planck Institute for Human Cognitive and Brain Sciences, Germany |
ISSN: | 1662-5129 1662-5129 |
DOI: | 10.3389/fnana.2021.725731 |