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Ladopoulou, J.

Publications and source records attributed to Ladopoulou, J..

2 recordsLinked to original sources

Within-Individual Precision Mapping of Brain Networks Exclusively Using Task Data

Precision mapping of brain networks within individuals has become a widely used tool that prevailingly relies on functional connectivity analysis of resting-state data. Here we explored whether networks could be precisely estimated solely using data acquired during active task paradigms. The straightforward strategy involved extracting residualized data after application of a task-based general linear model (GLM) and then applying standard functional connectivity analysis. Functional correlation matrices estimated from task data were highly similar to those derived from traditional resting-state fixation data. The largest factor affecting similarity between correlation matrices was the amount of data. Networks estimated within-individual from task data displayed strong spatial overlap with those estimated from resting-state fixation data and predicted the same triple functional dissociation in independent data. The implications of these findings are that (1) existing task data can be reanalyzed to estimate within-individual network organization, (2) restingstate fixation and task data can be pooled to increase statistical power, and (3) future studies can exclusively acquire task data to both estimate networks and extract task responses. Most broadly, the present results suggest that there is an underlying, stable network architecture that is idiosyncratic to the individual and persists across task states.

neuroscience↗

Within-Individual Organization of the Human Cerebral Cortex: Networks, Global Topography, and Function

The human cerebral cortex is populated by specialized regions that are organized into networks. Here we estimated networks using a Multi-Session Hierarchical Bayesian sModel (MS-HBM) applied to intensively sampled within-individual functional MRI (fMRI) data. The network estimation procedure was initially developed and tested in two participants (each scanned 31 times) and then prospectively applied to 15 new participants (each scanned 8 to 11 times). Detailed analysis of the networks revealed a global organization. Locally organized first-order sensory and motor networks were surrounded by spatially adjacent second-order networks that also linked to distant regions. Third-order networks each possessed regions distributed widely throughout association cortex. Moreover, regions of distinct third-order networks displayed side-by-side juxtapositions with a pattern that repeated similarly across multiple cortical zones. We refer to these as Supra-Areal Association Megaclusters (SAAMs). Within each SAAM, two candidate control regions were typically adjacent to three separate domain-specialized regions. Independent task data were analyzed to explore functional response properties. The somatomotor and visual first-order networks responded to body movements and visual stimulation, respectively. A subset of the second-order networks responded to transients in an oddball detection task, consistent with a role in orienting to salient or novel events. The third-order networks, including distinct regions within each SAAM, showed two levels of functional specialization. Regions linked to candidate control networks responded to working memory load across multiple stimulus domains. The remaining regions within each SAAM did not track working memory load but rather dissociated across language, social, and spatial / episodic processing domains. These results support a model of the cerebral cortex in which progressively higher-order networks nest outwards from primary sensory and motor cortices. Within the apex zones of association cortex there is specialization of large-scale networks that divides domain-flexible from domain-specialized regions repeatedly across parietal, temporal, and prefrontal cortices. We discuss implications of these findings including how repeating organizational motifs may emerge during development.

neuroscience↗