Surface anatomy and white matter connectivity of the premotor and motor areas

2021 ◽  
Author(s):  
Σπυρίδων Κωμαΐτης

ΣΚΟΠΟΣ: Σκοπός της παρούσας διατριβής είναι η μελέτη της αρχιτεκτονικής, της μορφολογίας και της συσχετιστικής ανατομίας των δεματίων λευκής ουσίας που εμπλέκονται στη συνδεσιμότητα του κινητικού και προκινητικού φλοιού καθώς και της επικουρικής και προ-εκπικουρικής περιοχής. ΜΕΘΟΔΟΣ: Τριάντα (30) ημισφαίρια υγειών ενηλίκων μονιμοποιημένα σε φορμόλη μελετήθηκαν με χρήση της μεθόδου παρασκευής της λευκής ουσίας κατά Klingler. Οι εν λόγω βήμα προς βήμα παρασκευές ολοκληρώθηκαν με κατεύθυνση από έξω προς τα έσω και από έσω προς τα έξω. ΑΠΟΤΕΛΕΣΜΑΤΑ: Αναζητήθηκε η υποφλοιώδης αρχιτεκτονική, η χωρική συσχέτιση και η συνδεσιμότητα τεσσάρων κυρίως μείζονων δεματίων: Α) Το ραχιαίο τμήμα του άνω επιμήκους δεματίου (SLF-I) ανευρέθηκε σταθερά στην έσω επιφάνεια του ημισφαιρίου να συνδέει το προσφηνοειδές λόβιο, την επικουρική και προ-επικουρική κινητική περιοχή. Β) Το Μετωπιαίο Επίμηκες Δεμάτιο(FLS) παρατηρήθηκε σταθερά ως μια πρόσθια συνέχεια του 2ου και 3ου τμήματος του άνω επιμήκους δεματίου(SLF II& SLF III). Το εν λόγω δεμάτιο συνδέει τον προκινητικό με τον προμετωπιαίο φλοιό. Γ) Το Μέτωπο-Κερκοφόρο Δεμάτιο (FCT) ένα ριπιδοειδές σύστημα ινών λευκής ουσίας, καταγράφηκε να συμμετέχει στη συνδεσιμότητα του προμετωπιαίου και προκινητικού φλοιού με την κεφαλή και το σώμα του κερκοφόρου πυρήνα. Δ) Το Φλοιο-καλυπτρικό δεμάτιο (CTT) ανευρέθηκε σταθερά να συνδέει τη μεσεγκεφαλική καλύπτρα με τον κινητικό/προκινητικό φλοιό και τον φλοιό της οπίσθιας κεντρικής έλικας. Κατά τις παρασκευές των εν λόγω δεματίων δεν παρατηρήθηκαν ημισφαιρικές ασυμμετρίες. Τέλος πρότυπα υποτμηματοποίησης προτάθηκαν για όλα τα δεμάτια. ΣΥΜΠΕΡΑΣΜΑΤΑ: Η συνδεσιμότητα και η λειτουργική εξειδίκευση των κινητικών και προκινητικών περιοχών του ανθρώπινου εγκεφάλου παραμένει σε μεγάλο βαθμό ασαφής καθώς ο μεγαλύτερος όγκος πληροφοριών προέρχεται από μελέτες σε πειραματόζωα και δεσμιδογραφικές μελέτες. Χρησιμοποιώντας την τεχνική Παρασκευής της λευκής ουσίας κατά Klingler ως βασική μέθοδο διερεύνησης, η παρούσα μελέτη παρέχει δεδομένα και στοιχεία για την λεπτή ανατομία των σχετιζόμενων με τις παραπάνω περιοχές δεματίων.

2021 ◽  
pp. 0271678X2199098
Author(s):  
Saima Hilal ◽  
Siwei Liu ◽  
Tien Yin Wong ◽  
Henri Vrooman ◽  
Ching-Yu Cheng ◽  
...  

To determine whether white matter network disruption mediates the association between MRI markers of cerebrovascular disease (CeVD) and cognitive impairment. Participants (n = 253, aged ≥60 years) from the Epidemiology of Dementia in Singapore study underwent neuropsychological assessments and MRI. CeVD markers were defined as lacunes, white matter hyperintensities (WMH), microbleeds, cortical microinfarcts, cortical infarcts and intracranial stenosis (ICS). White matter microstructure damage was measured as fractional anisotropy and mean diffusivity by tract based spatial statistics from diffusion tensor imaging. Cognitive function was summarized as domain-specific Z-scores. Lacunar counts, WMH volume and ICS were associated with worse performance in executive function, attention, language, verbal and visual memory. These three CeVD markers were also associated with white matter microstructural damage in the projection, commissural, association, and limbic fibers. Path analyses showed that lacunar counts, higher WMH volume and ICS were associated with executive and verbal memory impairment via white matter disruption in commissural fibers whereas impairment in the attention, visual memory and language were mediated through projection fibers. Our study shows that the abnormalities in white matter connectivity may underlie the relationship between CeVD and cognition. Further longitudinal studies are needed to understand the cause-effect relationship between CeVD, white matter damage and cognition.


Author(s):  
Jin Ho Jung ◽  
Yae Ji Kim ◽  
Seok Jong Chung ◽  
Han Soo Yoo ◽  
Yang Hyun Lee ◽  
...  

2018 ◽  
Vol 282 ◽  
pp. 47-54 ◽  
Author(s):  
Carolyn Beth McNabb ◽  
Rob Kydd ◽  
Frederick Sundram ◽  
Ian Soosay ◽  
Bruce Roy Russell

2020 ◽  
Author(s):  
Gina F. Humphreys ◽  
JeYoung Jung ◽  
Matthew A. Lambon Ralph

AbstractSeveral decades of neuropsychological and neuroimaging research have highlighted the importance of lateral parietal cortex (LPC) across a myriad of cognitive domains. Yet, despite the prominence of this region the underlying function of LPC remains unclear. Two domains that have placed particular emphasis on LPC involvement are semantic memory and episodic memory retrieval. From each domain, sophisticated models have been proposed as to the underlying function, as well as the more domain-general that LPC is engaged by any form of internally-directed cognition (episodic and semantic retrieval both being examples if this process). Here we directly address these alternatives using a combination of fMRI and DTI white-matter connectivity data. The results show that ventral LPC (angular gyrus) was positively engaged during episodic retrieval but disengaged during semantic memory retrieval. In addition, the level of activity negatively varied with task difficulty in the semantic task whereas episodic activation was independent of difficulty. In contrast, dorsal LPC (intraparietal sulcus) showed domain general activation that was positively correlated with task difficulty. In terms of structural connectivity, a dorsal-ventral and anterior-posterior gradient of connectivity was found to different processing networks (e.g., mid-angular gyrus (AG) connected with episodic retrieval). We propose a unifying model in which LPC as a whole might share a common underlying function (e.g., multimodal buffering) and variations across subregions arise due to differences in the underlying white matter connectivity.


2021 ◽  
Author(s):  
Ittai Shamir ◽  
Omri Tomer ◽  
Ronnie Krupnik ◽  
Yaniv Assaf

The human connectome is the complete structural description of the network of connections and elements that form the wiring diagram of the brain. Because of the current scarcity of information regarding laminar end points of white matter tracts inside cortical grey matter, tractography remains focused on cortical partitioning into regions, while ignoring radial partitioning into laminar components. To overcome this biased representation of the cortex as a single homogenous unit, we use a recent data-derived model of cortical laminar connectivity, which has been further explored and corroborated in the macaque brain by comparison to published studies. The model integrates multimodal MRI imaging datasets regarding both white matter connectivity and grey matter laminar composition into a laminar-level connectome. In this study we model the laminar connectome of healthy human brains (N=20) and explore them via a set of neurobiologically meaningful complex network measures. Our analysis demonstrates a subdivision of network hubs that appear in the standard connectome into each individual component of the laminar connectome, giving a fresh look into the role of laminar components in cortical connectivity and offering new prospects in the fields of both structural and functional connectivity.


2013 ◽  
Vol 28 (4) ◽  
pp. 325-334 ◽  
Author(s):  
Sophia van Hees ◽  
Katie McMahon ◽  
Anthony Angwin ◽  
Greig de Zubicaray ◽  
Stephen Read ◽  
...  

2020 ◽  
Vol 2 (2) ◽  
Author(s):  
Budhachandra Khundrakpam ◽  
Uku Vainik ◽  
Jinnan Gong ◽  
Noor Al-Sharif ◽  
Neha Bhutani ◽  
...  

Abstract Autism spectrum disorder is a highly prevalent and highly heritable neurodevelopmental condition, but studies have mostly taken traditional categorical diagnosis approach (yes/no for autism spectrum disorder). In contrast, an emerging notion suggests a continuum model of autism spectrum disorder with a normal distribution of autistic tendencies in the general population, where a full diagnosis is at the severe tail of the distribution. We set out to investigate such a viewpoint by investigating the interaction of polygenic risk scores for autism spectrum disorder and Age2 on neuroimaging measures (cortical thickness and white matter connectivity) in a general population (n = 391, with age ranging from 3 to 21 years from the Pediatric Imaging, Neurocognition and Genetics study). We observed that children with higher polygenic risk for autism spectrum disorder exhibited greater cortical thickness for a large age span starting from 3 years up to ∼14 years in several cortical regions localized in bilateral precentral gyri and the left hemispheric postcentral gyrus and precuneus. In an independent case–control dataset from the Autism Brain Imaging Data Exchange (n = 560), we observed a similar pattern: children with autism spectrum disorder exhibited greater cortical thickness starting from 6 years onwards till ∼14 years in wide-spread cortical regions including (the ones identified using the general population). We also observed statistically significant regional overlap between the two maps, suggesting that some of the cortical abnormalities associated with autism spectrum disorder overlapped with brain changes associated with genetic vulnerability for autism spectrum disorder in healthy individuals. Lastly, we observed that white matter connectivity between the frontal and parietal regions showed significant association with polygenic risk for autism spectrum disorder, indicating that not only the brain structure, but the white matter connectivity might also show a predisposition for the risk of autism spectrum disorder. Our findings showed that the fronto-parietal thickness and connectivity are dimensionally related to genetic risk for autism spectrum disorder in general population and are also part of the cortical abnormalities associated with autism spectrum disorder. This highlights the necessity of considering continuum models in studying the aetiology of autism spectrum disorder using polygenic risk scores and multimodal neuroimaging.


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