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      Anatomical Parcellations of Brodmann's Areas 4 and 6: A Study on Cortical Thickness for Improved Neurosurgical Planning

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          Abstract

          The cerebral cortex, comprising six layers known as the neocortex, is a sheet of neural tissue that contains regions for neurosurgical planning, including the primary motor cortex (PMC), the supplementary motor cortex (SMA), and the primary somatosensory cortex (PSC). However, knowledge gaps persist concerning the transition points between areas 3 to 4 and 4 to 6 and the SMA's extent. This study aims to develop a non-invasive protocol using T1/T2 weighted imaging to identify crucial anatomic borders around the primary and supplementary motor cortex for neurosurgical planning. A comprehensive literature search on the cytoarchitectonic borders of Brodmann's areas 3a, 4, and 6 was conducted, and relevant articles were selected based on their examination of these borders. The primary motor cortex was found to be the thickest region in the human brain, with discernible differences in thickness between areas 4 and 6. T2-weighted images revealed significant cortical thickness differences between the precentral and postcentral gyrus. Various methods have been employed to parcellate borders between cortical regions, including Laplace's equation and equi-volume models. A triple-layer appearance in the primary motor cortex and a novel method based on myelin content demonstrated consistent agreements with historically defined cytoarchitectonic borders. However, differentiating areas 4 and 6 from MR imaging remains challenging. Recent studies suggest potential methods for pre-surgically identifying the primary motor cortex and examining differences in cortical thickness in diseases. A protocol should be established to guide neurosurgeons in accurately identifying areas 4 and 6, possibly using imaging modalities superimposed on myelin maps for differentiation and determining area 6's anterior extent.

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          Most cited references14

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          SOMATIC MOTOR AND SENSORY REPRESENTATION IN THE CEREBRAL CORTEX OF MAN AS STUDIED BY ELECTRICAL STIMULATION

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            Mapping human cortical areas in vivo based on myelin content as revealed by T1- and T2-weighted MRI.

            Noninvasively mapping the layout of cortical areas in humans is a continuing challenge for neuroscience. We present a new method of mapping cortical areas based on myelin content as revealed by T1-weighted (T1w) and T2-weighted (T2w) MRI. The method is generalizable across different 3T scanners and pulse sequences. We use the ratio of T1w/T2w image intensities to eliminate the MR-related image intensity bias and enhance the contrast to noise ratio for myelin. Data from each subject were mapped to the cortical surface and aligned across individuals using surface-based registration. The spatial gradient of the group average myelin map provides an observer-independent measure of sharp transitions in myelin content across the surface--i.e., putative cortical areal borders. We found excellent agreement between the gradients of the myelin maps and the gradients of published probabilistic cytoarchitectonically defined cortical areas that were registered to the same surface-based atlas. For other cortical regions, we used published anatomical and functional information to make putative identifications of dozens of cortical areas or candidate areas. In general, primary and early unimodal association cortices are heavily myelinated and higher, multimodal, association cortices are more lightly myelinated, but there are notable exceptions in the literature that are confirmed by our results. The overall pattern in the myelin maps also has important correlations with the developmental onset of subcortical white matter myelination, evolutionary cortical areal expansion in humans compared with macaques, postnatal cortical expansion in humans, and maps of neuronal density in non-human primates.
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              Anatomically motivated modeling of cortical laminae.

              Improvements in the spatial resolution of structural and functional MRI are beginning to enable analysis of intracortical structures such as heavily myelinated layers in 3D, a prerequisite for in-vivo parcellation of individual human brains. This parcellation can only be performed precisely if the profiles used in cortical analysis are anatomically meaningful. Profiles are often constructed as traverses that are perpendicular to computed laminae. In this case they are fully determined by these laminae. The aim of this study is to evaluate models for cortical laminae used so far and to establish a new model. Methods to model the laminae used so far include constructing laminae that keep a constant distance to the cortical boundaries, so-called equidistant laminae. Another way is to compute equipotentials between the cortical boundary surfaces with the Laplace equation. The Laplace profiles resulting from the gradients to the equipotentials were often-used because of their nice mathematical properties. However, the equipotentials these Laplacian profiles are constructed from and the equidistant laminae do not follow the anatomical layers observed using high resolution MRI of cadaver brain. To remedy this problem, we introduce a novel equi-volume model that derives from work by Bok (1929). He argued that cortical segments preserve their volume, while layer thickness changes to compensate cortical folding. We incorporate this preservation of volume in our new equi-volume model to generate a three-dimensional well-adapted undistorted coordinate system of the cortex. When defined by this well-adapted coordinate system, cortical depth is anatomically meaningful. We compare isocontours from these cortical depth values to locations of myelinated bands on high-resolution ex-vivo and in-vivo three-dimensional MR images. A similar comparison was performed with equipotentials computed with the Laplace equation and with equidistant isocontours. A quantitative evaluation of the equi-volume model using measured image intensities confirms that it provides a much better fit to observed cortical layering.
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                Author and article information

                Journal
                Cureus
                Cureus
                2168-8184
                Cureus
                Cureus (Palo Alto (CA) )
                2168-8184
                2 July 2023
                July 2023
                : 15
                : 7
                : e41280
                Affiliations
                [1 ] Neurological Surgery, Mayo Clinic, Rochester, USA
                [2 ] Neurology, Mayo Clinic, Rochester, USA
                Author notes
                Article
                10.7759/cureus.41280
                10315162
                b6664759-0020-4f6b-b2a3-2daa03f6e7e6
                Copyright © 2023, Alan et al.

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 2 July 2023
                Categories
                Neurology
                Neurosurgery
                Anatomy

                primary somatosensory cortex,layer v,betz cell,parcellations,divisions,supplementary motor cortex,primary motor cortex,area 6,area 4,korbinian brodmann

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