Abstract
Though linked to an unusually broad array of functions, the human claustrum's complex morphology has hindered in vivo study, resulting in a small MRI literature marked by implausibly large discrepancies in reported characteristics. We constructed the first three-dimensional histological "gold standard" claustrum model, and systematically evaluated in vivo 7-Tesla MRI datasets against it and downsampled derivatives. MRI showed resolution-dependent differences rather than contrast limitations, transforming the claustrum's intricate sheet into an artefactually thickened ribbon. However, submillimetre MRI reliably recovered the dorsal "core" that contains most claustral volume and density and houses major corticoclaustral connectivity. At 0.5mm resolution, extension into the temporal lobe, including irregular ventral "puddles", was partially recovered, with uncertainty reflecting boundary imprecision rather than anatomical loss. Our results refute the view that the claustrum is inaccessible in the living human brain, define practical measurement limits, and provide a foundation for future functional investigations.
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ABSTRACT
Though linked to an unusually broad array of functions, the human claustrum’s complex morphology has hindered in vivo study, resulting in a small MRI literature marked by implausibly large discrepancies in reported characteristics. We constructed the first three-dimensional histological “gold standard” claustrum model, and systematically evaluated in vivo 7-Tesla MRI datasets against it and downsampled derivatives. MRI showed resolution-dependent differences rather than contrast limitations, transforming the claustrum’s intricate sheet into an artefactually thickened ribbon. However, submillimetre MRI reliably recovered the dorsal “core” that contains most claustral volume and density and houses major corticoclaustral connectivity. At 0.5mm resolution, extension into the temporal lobe, including irregular ventral “puddles”, was partially recovered, with uncertainty reflecting boundary imprecision rather than anatomical loss. Our results refute the view that the claustrum is inaccessible in the living human brain, define practical measurement limits, and provide a foundation for future functional investigations.
Competing Interest Statement
The authors have declared no competing interest.
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