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 inFrontiers in neuroanatomy Vol. 15; p. 725731
Main Authors Kumar, Vinod Jangir, Scheffler, Klaus, Hagberg, Gisela E., Grodd, Wolfgang
Format Journal Article
LanguageEnglish
Published Lausanne Frontiers Research Foundation 16.09.2021
Frontiers Media S.A
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ISSN1662-5129
1662-5129
DOI10.3389/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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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