Displaying 1 - 20 of 20
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Amunts, K., Axer, M., Banerjee, S., Bitsch, L., Bjaalie, J. G., Brauner, P., Brovelli, A., Calarco, N., Carrere, M., Caspers, S., Charvet, C. J., Cichon, S., Cools, R., Costantini, I., D’Angelo, E. U., Bonis, G. D., Deco, G., DeFelipe, J., Destexhe, A., Dickscheid, T. Amunts, K., Axer, M., Banerjee, S., Bitsch, L., Bjaalie, J. G., Brauner, P., Brovelli, A., Calarco, N., Carrere, M., Caspers, S., Charvet, C. J., Cichon, S., Cools, R., Costantini, I., D’Angelo, E. U., Bonis, G. D., Deco, G., DeFelipe, J., Destexhe, A., Dickscheid, T., Diesmann, M., Düzel, E., Eickhoff, S. B., Einevoll, G., Eke, D., Engel, A. K., Evans, A. C., Evers, K., Fedorchenko, N., Forkel, S. J., Fousek, J., Friederici, A. D., Friston, K., Furber, S., Geris, L., Goebel, R., Güntürkün, O., Hamid, A. I. A., Herold, C., Hilgetag, C. C., Hölter, S. M., Ioannidis, Y., Jirsa, V., Kashyap, S., Kasper, B. S., Kerchove de d’Exaerde, A., Kooijmans, R., Koren, I., Kotaleski, J. H., Kiar, G., Klijn, W., Klüver, L., Knoll, A. C., Krsnik, Z., Kämpfer, J., Larkum, M. E., Linne, M.-L., Lippert, T., Malin Abdullah, J. M., Maio, P. D., Magielse, N., Maquet, P., Mascaro, A. L. A., Marinazzo, D., Mejias, J., Meyer-Lindenberg, A., Migliore, M., Michael, J., Morel, Y., Morin, F. O., Muckli, L., Nagels, G., Oden, L., Palomero-Gallagher, N., Panagiotaropoulos, F., Paolucci, P. S., Pennartz, C., Peeters, L. M., Petkoski, S., Petkov, N., Petro, L. S., Petrovici, M. A., Pezzulo, G., Roelfsema, P., Ris, L., Ritter, P., Rockland, K., Rotter, S., Rowald, A., Ruland, S., Ryvlin, P., Salles, A., Sanchez-Vives, M. V., Schemmel, J., Senn, W., De Sousa, A. A., Ströckens, F., Thirion, B., Uludağ, K., Vanni, S., Van Albada, S. J., Vanduffel, W., Vezoli, J., Vincenz-Donnelly, L., Walter, F., & Zaborszky, L. (2024). The coming decade of digital brain research: A vision for neuroscience at the intersection of technology and computing. Imaging Neuroscience, 2, 1-35. doi:10.1162/imag_a_00137.
Abstract
In recent years, brain research has indisputably entered a new epoch, driven by substantial methodological advances and digitally enabled data integration and modelling at multiple scales—from molecules to the whole brain. Major advances are emerging at the intersection of neuroscience with technology and computing. This new science of the brain combines high-quality research, data integration across multiple scales, a new culture of multidisciplinary large-scale collaboration, and translation into applications. As pioneered in Europe’s Human Brain Project (HBP), a systematic approach will be essential for meeting the coming decade’s pressing medical and technological challenges. The aims of this paper are to: develop a concept for the coming decade of digital brain research, discuss this new concept with the research community at large, identify points of convergence, and derive therefrom scientific common goals; provide a scientific framework for the current and future development of EBRAINS, a research infrastructure resulting from the HBP’s work; inform and engage stakeholders, funding organisations and research institutions regarding future digital brain research; identify and address the transformational potential of comprehensive brain models for artificial intelligence, including machine learning and deep learning; outline a collaborative approach that integrates reflection, dialogues, and societal engagement on ethical and societal opportunities and challenges as part of future neuroscience research. -
Andrulyte, I., De Bezenac, C., Branzi, F., Forkel, S. J., Taylor, P. N., & Keller, S. S. (2024). The relationship between white matter architecture and language lateralisation in the healthy brain. The Journal of Neuroscience, 44(50): e0166242024. doi:10.1523/JNEUROSCI.0166-24.2024.
Abstract
Interhemispheric anatomical asymmetries have long been thought to be related to language lateralisation. Previous studies have explored whether asymmetries in the diffusion characteristics of white matter language tracts are consistent with language lateralisation. These studies, typically with smaller cohorts, yielded mixed results. This study investigated whether connectomic analysis of quantitative anisotropy (QA) and shape features of white matter tracts across the whole brain are associated with language lateralisation. We analysed 1040 healthy individuals from the Human Connectome Project database. Hemispheric language dominance for each participant was quantified using a laterality quotient (LQ) derived from fMRI activation in regions of interest (ROIs) associated with a language comprehension task compared against a math task. A linear regression model was used to examine the relationship between structural asymmetry and functional lateralisation. Connectometry revealed that LQs were significantly negatively correlated with QA of corpus callosum tracts, including forceps minor, body, tapetum, and forceps major, indicating that reduced language dominance (more bilateral language representation) is associated with increased QA in these regions. The QA of the left arcuate fasciculus, cingulum, and right cerebellar tracts was positively associated with LQ, suggesting that stronger structural asymmetry in these tracts may identify left language dominance. Language lateralisation was not significantly associated with the shape metrics (including length, span, curl, elongation, diameter, volume, and surface area) of all white matter tracts. These results suggest that diffusion measures of microstructural architecture, and not the geometric features of reconstructed white matter tracts, are associated with lateralisation of language comprehension functions. People with increased dependence on both cerebral hemispheres for language processing may have more developed commissural fibres, which may support more efficient interhemispheric communication. -
Basile, G. A., Nozais, V., Quartarone, A., Giustiniani, A., Ielo, A., Cerasa, A., Milardi, D., Abdallah, M., Thiebaut de Schotten, M., Forkel, S. J., & Cacciola, A. (2024). Functional anatomy and topographical organization of the frontotemporal arcuate fasciculus. Communications Biology, 7: 1655. doi:10.1038/s42003-024-07274-3.
Abstract
Traditionally, the frontotemporal arcuate fasciculus (AF) is viewed as a single entity in anatomo-clinical models. However, it is unclear if distinct cortical origin and termination patterns within this bundle correspond to specific language functions. We use track-weighted dynamic functional connectivity, a hybrid imaging technique, to study the AF structure and function in two distinct datasets of healthy subjects. Here we show that the AF can be subdivided based on dynamic changes in functional connectivity at the streamline endpoints. An unsupervised parcellation algorithm reveals spatially segregated subunits, which are then functionally quantified through meta-analysis. This approach identifies three distinct clusters within the AF - ventral, middle, and dorsal frontotemporal AF - each linked to different frontal and temporal termination regions and likely involved in various language production and comprehension aspects. Our findings may have relevant implications for the understanding of the functional anatomy of the AF as well as its contribution to linguistic and non-linguistic functions.Additional information
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Della Sala, S., Bathelt, J., Buchtel, H., Tavano, A., Press, C., Love, B., Croy, I., Morris, R., Kotz, S., Kopelman, M. D., Coco, M. I., Reber, P., Forkel, S. J., & Schweinberger, S. R. (2024). The future of science publishing. Cortex, 181, 93-100. doi:10.1016/j.cortex.2024.10.005.
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Forkel, S. J., & Hagoort, P. (2024). Redefining language networks: Connectivity beyond localised regions. Brain Structure & Function, 229, 2073-2078. doi:10.1007/s00429-024-02859-4.
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Guzmán Chacón, E., Ovando-Tellez, M., Thiebaut de Schotten, M., & Forkel, S. J. (2024). Embracing digital innovation in neuroscience: 2023 in review at NEUROCCINO. Brain Structure & Function, 229, 251-255. doi:10.1007/s00429-024-02768-6.
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Hope, T. M. H., Neville, D., Talozzi, L., Foulon, C., Forkel, S. J., Thiebaut de Schotten, M., & Price, C. J. (2024). Testing the disconnectome symptom discoverer model on out-of-sample post-stroke language outcomes. Brain, 147(2), e11-e13. doi:10.1093/brain/awad352.
Abstract
Stroke is common, and its consequent brain damage can cause various cognitive impairments. Associations between where and how much brain lesion damage a patient has suffered, and the particular impairments that injury has caused (lesion-symptom associations) offer potentially compelling insights into how the brain implements cognition.1 A better understanding of those associations can also fill a gap in current stroke medicine by helping us to predict how individual patients might recover from post-stroke impairments.2 Most recent work in this area employs machine learning models trained with data from stroke patients whose mid-to-long-term outcomes are known.2-4 These machine learning models are tested by predicting new outcomes—typically scores on standardized tests of post-stroke impairment—for patients whose data were not used to train the model. Traditionally, these validation results have been shared in peer-reviewed publications describing the model and its training. But recently, and for the first time in this field (as far as we know), one of these pre-trained models has been made public—The Disconnectome Symptom Discoverer model (DSD) which draws its predictors from structural disconnection information inferred from stroke patients’ brain MRI.5
Here, we test the DSD model on wholly independent data, never seen by the model authors, before they published it. Specifically, we test whether its predictive performance is just as accurate as (i.e. not significantly worse than) that reported in the original (Washington University) dataset, when predicting new patients’ outcomes at a similar time post-stroke (∼1 year post-stroke) and also in another independent sample tested later (5+ years) post-stroke. A failure to generalize the DSD model occurs if it performs significantly better in the Washington data than in our data from patients tested at a similar time point (∼1 year post-stroke). In addition, a significant decrease in predictive performance for the more chronic sample would be evidence that lesion-symptom associations differ at ∼1 year post-stroke and >5 years post-stroke. -
Pacella, V., Nozais, V., Talozzi, L., Abdallah, M., Wassermann, D., Forkel, S. J., & Thiebaut de Schotten, M. (2024). The morphospace of the brain-cognition organisation. Nature Communications, 15: 8452. doi:10.1038/s41467-024-52186-9.
Abstract
Over the past three decades, functional neuroimaging has amassed abundant evidence of the intricate interplay between brain structure and function. However, the potential anatomical and experimental overlap, independence, granularity, and gaps between functions remain poorly understood. Here, we show the latent structure of the current brain-cognition knowledge and its organisation. Our approach utilises the most comprehensive meta-analytic fMRI database (Neurosynth) to compute a three-dimensional embedding space–morphospace capturing the relationship between brain functions as we currently understand them. The space structure enables us to statistically test the relationship between functions expressed as the degree to which the characteristics of each functional map can be anticipated based on its similarities with others–the predictability index. The morphospace can also predict the activation pattern of new, unseen functions and decode thoughts and inner states during movie watching. The framework defined by the morphospace will spur the investigation of novel functions and guide the exploration of the fabric of human cognition.Additional information
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Barrett, R. L. C., Dawson, M., Dyrby, T. B., Krug, K., Ptito, M., D'Arceuil, H., Croxson, P. L., Johnson, P. J., Howells, H., Forkel, S. J., Dell'Acqua, F., & Catani, M. (2020). Differences in Frontal Network Anatomy Across Primate Species. The Journal of Neuroscience, 40(10), 2094-2107. doi:10.1523/JNEUROSCI.1650-18.2019.
Abstract
The frontal lobe is central to distinctive aspects of human cognition and behavior. Some comparative studies link this to a larger frontal cortex and even larger frontal white matter in humans compared with other primates, yet others dispute these findings. The discrepancies between studies could be explained by limitations of the methods used to quantify volume differences across species, especially when applied to white matter connections. In this study, we used a novel tractography approach to demonstrate that frontal lobe networks, extending within and beyond the frontal lobes, occupy 66% of total brain white matter in humans and 48% in three monkey species: vervets (Chlorocebus aethiops), rhesus macaque (Macaca mulatta) and cynomolgus macaque (Macaca fascicularis), all male. The simian–human differences in proportional frontal tract volume were significant for projection, commissural, and both intralobar and interlobar association tracts. Among the long association tracts, the greatest difference was found for tracts involved in motor planning, auditory memory, top-down control of sensory information, and visuospatial attention, with no significant differences in frontal limbic tracts important for emotional processing and social behaviour. In addition, we found that a nonfrontal tract, the anterior commissure, had a smaller volume fraction in humans, suggesting that the disproportionally large volume of human frontal lobe connections is accompanied by a reduction in the proportion of some nonfrontal connections. These findings support a hypothesis of an overall rearrangement of brain connections during human evolution. -
Forkel, S. J., Rogalski, E., Drossinos Sancho, N., D'Anna, L., Luque Laguna, P., Sridhar, J., Dell'Acqua, F., Weintraub, S., Thompson, C., Mesulam, M.-M., & Catani, M. (2020). Anatomical evidence of an indirect pathway for word repetition. Neurology, 94, e594-e606. doi:10.1212/WNL.0000000000008746.
Abstract
Objective: To combine MRI-based cortical morphometry and diffusion white matter tractography to describe the anatomical correlates of repetition deficits in patients with primary progressive aphasia (PPA).
Methods: The traditional anatomical model of language identifies a network for word repetition that includes Wernicke and Broca regions directly connected via the arcuate fasciculus. Recent tractography findings of an indirect pathway between Wernicke and Broca regions suggest a critical role of the inferior parietal lobe for repetition. To test whether repetition deficits are associated with damage to the direct or indirect pathway between both regions, tractography analysis was performed in 30 patients with PPA (64.27 ± 8.51 years) and 22 healthy controls. Cortical volume measurements were also extracted from 8 perisylvian language areas connected by the direct and indirect pathways.
Results: Compared to healthy controls, patients with PPA presented with reduced performance in repetition tasks and increased damage to most of the perisylvian cortical regions and their connections through the indirect pathway. Repetition deficits were prominent in patients with cortical atrophy of the temporo-parietal region with volumetric reductions of the indirect pathway.
Conclusions: The results suggest that in PPA, deficits in repetition are due to damage to the temporo-parietal cortex and its connections to Wernicke and Broca regions. We therefore propose a revised language model that also includes an indirect pathway for repetition, which has important clinical implications for the functional mapping and treatment of neurologic patients. -
Forkel, S. J., & Thiebaut de Schotten, M. (2020). Towards metabolic disconnection – symptom mapping. Brain, 143(3), 718-721. doi:10.1093/brain/awaa060.
Abstract
This scientific commentary refers to ‘Metabolic lesion-deficit mapping of human cognition’ by Jha etal. -
Friedrich, P., Forkel, S. J., & Thiebaut de Schotten, M. (2020). Mapping the principal gradient onto the corpus callosum. NeuroImage, 223: 117317. doi:10.1016/j.neuroimage.2020.117317.
Abstract
Gradients capture some of the variance of the resting-state functional magnetic resonance imaging (rsfMRI) signal. Amongst these, the principal gradient depicts a functional processing hierarchy that spans from sensory-motor cortices to regions of the default-mode network. While the cortex has been well characterised in terms of gradients little is known about its underlying white matter. For instance, comprehensive mapping of the principal gradient on the largest white matter tract, the corpus callosum, is still missing. Here, we mapped the principal gradient onto the midsection of the corpus callosum using the 7T human connectome project dataset. We further explored how quantitative measures and variability in callosal midsection connectivity relate to the principal gradient values. In so doing, we demonstrated that the extreme values of the principal gradient are located within the callosal genu and the posterior body, have lower connectivity variability but a larger spatial extent along the midsection of the corpus callosum than mid-range values. Our results shed light on the relationship between the brain's functional hierarchy and the corpus callosum. We further speculate about how these results may bridge the gap between functional hierarchy, brain asymmetries, and evolution.Additional information
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Friedrich, P., Thiebaut de Schotten, M., Forkel, S. J., Stacho, M., & Howells, H. (2020). An ancestral anatomical and spatial bias for visually guided behavior. Proceedings of the National Academy of Sciences of the United States of America, 117(5), 2251-2252. doi:10.1073/pnas.1918402117.
Abstract
Human behavioral asymmetries are commonly studied in the context of structural cortical and connectional asymmetries. Within this framework, Sreenivasan and Sridharan (1) provide intriguing evidence of a relationship between visual asymmetries and the lateralization of superior colliculi connections—a phylogenetically older mesencephalic structure. Specifically, response facilitation for cued locations (i.e., choice bias) in the contralateral hemifield was associated with differences in the connectivity of the superior colliculus. Given that the superior colliculus has a structural homolog—the optic tectum—which can be traced across all Vertebrata, these results may have meaningful evolutionary ramifications. -
Howells, H., Puglisi, G., Leonetti, A., Vigano, L., Fornia, L., Simone, L., Forkel, S. J., Rossi, M., Riva, M., Cerri, G., & Bello, L. (2020). The role of left fronto-parietal tracts in hand selection: Evidence from neurosurgery. Cortex, 128, 297-311. doi:10.1016/j.cortex.2020.03.018.
Abstract
Strong right-hand preference on the population level is a uniquely human feature, although its neural basis is still not clearly defined. Recent behavioural and neuroimaging literature suggests that hand preference may be related to the orchestrated function and size of fronto-parietal white matter tracts bilaterally. Lesions to these tracts induced during tumour resection may provide an opportunity to test this hypothesis. In the present study, a cohort of seventeen neurosurgical patients with left hemisphere brain tumours were recruited to investigate whether resection of certain white matter tracts affects the choice of hand selected for the execution of a goal-directed task (assembly of jigsaw puzzles). Patients performed the puzzles, but also tests for basic motor ability, selective attention and visuo-constructional ability, preoperatively and one month after surgery. An atlas-based disconnectome analysis was conducted to evaluate whether resection of tracts was significantly associated with changes in hand selection. Diffusion tractography was also used to dissect fronto-parietal tracts (the superior longitudinal fasciculus) and the corticospinal tract. Results showed a shift in hand selection despite the absence of any motor or cognitive deficits, which was significantly associated with frontal and parietal resections rather than other lobes. In particular, the shift in hand selection was significantly associated with the resection of dorsal rather than ventral fronto-parietal white matter connections. Dorsal white matter pathways contribute bilaterally to control of goal-directed hand movements. We show that unilateral lesions, that may unbalance the cooperation of the two hemispheres, can alter the choice of hand selected to accomplish movements. -
Milham, M., Petkov, C. I., Margulies, D. S., Schroeder, C. E., Basso, M. A., Belin, P., Fair, D. A., Fox, A., Kastner, S., Mars, R. B., Messinger, A., Poirier, C., Vanduffel, W., Van Essen, D. C., Alvand, A., Becker, Y., Ben Hamed, S., Benn, A., Bodin, C., Boretius, S. Milham, M., Petkov, C. I., Margulies, D. S., Schroeder, C. E., Basso, M. A., Belin, P., Fair, D. A., Fox, A., Kastner, S., Mars, R. B., Messinger, A., Poirier, C., Vanduffel, W., Van Essen, D. C., Alvand, A., Becker, Y., Ben Hamed, S., Benn, A., Bodin, C., Boretius, S., Cagna, B., Coulon, O., El-Gohary, S. H., Evrard, H., Forkel, S. J., Friedrich, P., Froudist-Walsh, S., Garza-Villarreal, E. A., Gao, Y., Gozzi, A., Grigis, A., Hartig, R., Hayashi, T., Heuer, K., Howells, H., Ardesch, D. J., Jarraya, B., Jarrett, W., Jedema, H. P., Kagan, I., Kelly, C., Kennedy, H., Klink, P. C., Kwok, S. C., Leech, R., Liu, X., Madan, C., Madushanka, W., Majka, P., Mallon, A.-M., Marche, K., Meguerditchian, A., Menon, R. S., Merchant, H., Mitchell, A., Nenning, K.-H., Nikolaidis, A., Ortiz-Rios, M., Pagani, M., Pareek, V., Prescott, M., Procyk, E., Rajimehr, R., Rautu, I.-S., Raz, A., Roe, A. W., Rossi-Pool, R., Roumazeilles, L., Sakai, T., Sallet, J., García-Saldivar, P., Sato, C., Sawiak, S., Schiffer, M., Schwiedrzik, C. M., Seidlitz, J., Sein, J., Shen, Z.-m., Shmuel, A., Silva, A. C., Simone, L., Sirmpilatze, N., Sliwa, J., Smallwood, J., Tasserie, J., Thiebaut de Schotten, M., Toro, R., Trapeau, R., Uhrig, L., Vezoli, J., Wang, Z., Wells, S., Williams, B., Xu, T., Xu, A. G., Yacoub, E., Zhan, M., Ai, L., Amiez, C., Balezeau, F., Baxter, M. G., Blezer, E. L., Brochier, T., Chen, A., Croxson, P. L., Damatac, C. G., Dehaene, S., Everling, S., Fleysher, L., Freiwald, W., Griffiths, T. D., Guedj, C., Hadj-Bouziane, F., Harel, N., Hiba, B., Jung, B., Koo, B., Laland, K. N., Leopold, D. A., Lindenfors, P., Meunier, M., Mok, K., Morrison, J. H., Nacef, J., Nagy, J., Pinsk, M., Reader, S. M., Roelfsema, P. R., Rudko, D. A., Rushworth, M. F., Russ, B. E., Schmid, M. C., Sullivan, E. L., Thiele, A., Todorov, O. S., Tsao, D., Ungerleider, L., Wilson, C. R., Ye, F. Q., Zarco, W., & Zhou, Y.-d. (2020). Accelerating the Evolution of Nonhuman Primate Neuroimaging. Neuron, 105(4), 600-603. doi:10.1016/j.neuron.2019.12.023.
Abstract
Nonhuman primate neuroimaging is on the cusp of a transformation, much in the same way its human counterpart was in 2010, when the Human Connectome Project was launched to accelerate progress. Inspired by an open data-sharing initiative, the global community recently met and, in this article, breaks through obstacles to define its ambitions.Additional information
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Waymel, A., Friedrich, P., Bastian, P.-A., Forkel, S. J., & Thiebaut de Schotten, M. (2020). Anchoring the human olfactory system within a functional gradient. NeuroImage, 216: 116863. doi:10.1016/j.neuroimage.2020.116863.
Abstract
Margulies et al. (2016) demonstrated the existence of at least five independent functional connectivity gradients in the human brain. However, it is unclear how these functional gradients might link to anatomy. The dual origin theory proposes that differences in cortical cytoarchitecture originate from two trends of progressive differentiation between the different layers of the cortex, referred to as the hippocampocentric and olfactocentric systems. When conceptualising the functional connectivity gradients within the evolutionary framework of the Dual Origin theory, the first gradient likely represents the hippocampocentric system anatomically. Here we expand on this concept and demonstrate that the fifth gradient likely links to the olfactocentric system. We describe the anatomy of the latter as well as the evidence to support this hypothesis. Together, the first and fifth gradients might help to model the Dual Origin theory of the human brain and inform brain models and pathologies. -
Croxson, P., Forkel, S. J., Cerliani, L., & Thiebaut De Schotten, M. (2018). Structural Variability Across the Primate Brain: A Cross-Species Comparison. Cerebral Cortex, 28(11), 3829-3841. doi:10.1093/cercor/bhx244.
Abstract
A large amount of variability exists across human brains; revealed initially on a small scale by postmortem studies and,
more recently, on a larger scale with the advent of neuroimaging. Here we compared structural variability between human
and macaque monkey brains using grey and white matter magnetic resonance imaging measures. The monkey brain was
overall structurally as variable as the human brain, but variability had a distinct distribution pattern, with some key areas
showing high variability. We also report the first evidence of a relationship between anatomical variability and evolutionary
expansion in the primate brain. This suggests a relationship between variability and stability, where areas of low variability
may have evolved less recently and have more stability, while areas of high variability may have evolved more recently and
be less similar across individuals. We showed specific differences between the species in key areas, including the amount of
hemispheric asymmetry in variability, which was left-lateralized in the human brain across several phylogenetically recent
regions. This suggests that cerebral variability may be another useful measure for comparison between species and may add
another dimension to our understanding of evolutionary mechanisms.Additional information
supplementary file supplementary table 1 supplementary table 2 supplementary figure 1 supplementary figure 2 -
Forkel, S. J., & Catani, M. (2018). Lesion mapping in acute stroke aphasia and its implications for recovery. Neuropsychologia, 115, 88-100. doi:10.1016/j.neuropsychologia.2018.03.036.
Abstract
Patients with stroke offer a unique window into understanding human brain function. Mapping stroke lesions poses several challenges due to the complexity of the lesion anatomy and the mechanisms causing local and remote disruption on brain networks. In this prospective longitudinal study, we compare standard and advanced approaches to white matter lesion mapping applied to acute stroke patients with aphasia. Eighteen patients with acute left hemisphere stroke were recruited and scanned within two weeks from symptom onset. Aphasia assessment was performed at baseline and six-month follow-up. Structural and diffusion MRI contrasts indicated an area of maximum overlap in the anterior external/extreme capsule with diffusion images showing a larger overlap extending into posterior perisylvian regions. Anatomical predictors of recovery included damage to ipsilesional tracts (as shown by both structural and diffusion images) and contralesional tracts (as shown by diffusion images only). These findings indicate converging results from structural and diffusion lesion mapping methods but also clear differences between the two approaches in their ability to identify predictors of recovery outside the lesioned regions. -
Forkel, S. J., & Catani, M. (2018). Structural Neuroimaging. In A. De Groot, & P. Hagoort (
Eds. ), Research Methods in Psycholinguistics and the Neurobiology of Language: A Practical Guide (pp. 288-308). Hoboken: Wiley. doi:10.1002/9781394259762.ch15.Abstract
Structural imaging based on computerized tomography (CT) and magnetic resonance imaging (MRI) has progressively replaced traditional post‐mortem studies in the process of identifying the neuroanatomical basis of language. In the clinical setting, the information provided by structural imaging has been used to confirm the exact diagnosis and formulate an individualized treatment plan. In the research arena, neuroimaging has permitted to understand neuroanatomy at the individual and group level. The possibility to obtain quantitative measures of lesions has improved correlation analyses between severity of symptoms, lesion load, and lesion location. More recently, the development of structural imaging based on diffusion MRI has provided valid solutions to two major limitations of more conventional imaging. In stroke patients, diffusion can visualize early changes due to a stroke that are otherwise not detectable with more conventional structural imaging, with important implications for the clinical management of acute stroke patients. Beyond the sensitivity to early changes, diffusion imaging tractography presents the possibility of visualizing the trajectories of individual white matter pathways connecting distant regions. A pathway analysis based on tractography is offering a new perspective in neurolinguistics. First, it permits to formulate new anatomical models of language function in the healthy brain and allows to directly test these models in the human population without any reliance on animal models. Second, by defining the exact location of the damage to specific white matter connections we can understand the contribution of different mechanisms to the emergence of language deficits (e.g., cortical versus disconnection mechanisms). Finally, a better understanding of the anatomical variability of different language networks is helping to identify new anatomical predictors of language recovery. In this chapter we will focus on the principles of structural MRI and, in particular, diffusion imaging and tractography and present examples of how these methods have informed our understanding of variance in language performances in the healthy brain and language deficits in patient populations. -
Vanderauwera, J., De Vos, A., Forkel, S. J., Catani, M., Wouters, J., Vandermosten, M., & Ghesquière, P. (2018). Neural organization of ventral white matter tracts parallels the initial steps of reading development: A DTI tractography study. Brain and Language, 183, 32-40. doi:10.1016/j.bandl.2018.05.007.
Abstract
Insight in the developmental trajectory of the neuroanatomical reading correlates is important to understand related cognitive processes and disorders. In adults, a dual pathway model has been suggested encompassing a dorsal phonological and a ventral orthographic white matter system. This dichotomy seems not present in pre-readers, and the specific role of ventral white matter in reading remains unclear. Therefore, the present longitudinal study investigated the relation between ventral white matter and cognitive processes underlying reading in children with a broad range of reading skills (n = 61). Ventral pathways of the reading network were manually traced using diffusion tractography: the inferior fronto-occipital fasciculus (IFOF), inferior longitudinal fasciculus (ILF) and uncinate fasciculus (UF). Pathways were examined pre-reading (5–6 years) and after two years of reading acquisition (7–8 years). Dimension reduction for the cognitive measures resulted in one component for pre-reading cognitive measures and a separate phonological and orthographic component for the early reading measures. Regression analyses revealed a relation between the pre-reading cognitive component and bilateral IFOF and left ILF. Interestingly, exclusively the left IFOF was related to the orthographic component, whereas none of the pathways was related to the phonological component. Hence, the left IFOF seems to serve as the lexical reading route, already in the earliest reading stages.
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