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Xiang, J. D.

Publications and source records attributed to Xiang, J. D..

4 recordsLinked to original sources

Individualized parcellation reveals functional boundaries in human prefrontal cortex

Human prefrontal cortex (PFC) supports diverse higher-order cognitive functions during task execution. Increasing evidence suggests that these functions are organized along large-scale gradients, such as a rostro-caudal axis supporting progressively abstract-to-concrete information processing. At the same time, regional specialization within PFC, including focal patches selective for specific stimulus categories, suggests the presence of discrete functional boundaries. Whether PFC organization is best characterized by continuous gradients or discrete subdivisions remains unresolved. Here we show that task-evoked functional organization in PFC exhibits substantial inter-individual variability, limiting the usefulness of conventional group atlases in testing for functional boundaries. To address this challenge, we estimated individualized functional parcellations by combining a group atlas with task-evoked fMRI data spanning diverse cognitive tasks. The group atlas revealed large-scale functional gradients across PFC, whereas individualized parcellations additionally uncovered sharp functional boundaries obscured by group averaging. Moreover, functional organization in PFC was substantially more fine-grained than in other association cortices, consistent with its integrative role in cognitive control. Together, these findings suggest that PFC organization reflects an individualized mosaic of fine-grained functional subdivisions embedded within broader large-scale gradients, with important implications for defining core constructs such as the multiple-demand system.

neuroscience↗

Multi-Task Batteries for Precision Functional Mapping

Functional brain mapping is an important tool to understand the organization of the human brain, both at the group level, but also to an increasing degree at the level of the individual. There are currently two main approaches to do so. Resting-state fMRI relies on inter-regional correlations of random fluctuations of the signal. In contrast, task-based localizers typically use a single-contrast between a task of interest and a matched control task to identify the location of a functional region in an individual brain. In this paper, we propose and evaluate a third approach: the use of multi-task batteries for both localization of a single functional region and parcellation of multiple functional regions. We show that multi-task localizers produce more consistent estimation of a single functional region across subjects than the single-contrast approach using the same amount of fMRI data. Furthermore, we demonstrate that the multi-task approach is sensitive to true inter-individual differences in region size, and does not suffer the same influence of signal-to-noise ratio that biases the single-contrast localizer. We then address the question of how to select tasks for the battery, and present a data-driven strategy that optimizes the characterization of a brain structure of interest. We show that such batteries outperform randomly selected batteries both for building individual parcellations as well as individual connectivity models. Finally, we demonstrate that an interspersed design - where all tasks are presented in each imaging run - yields more reliable results than splitting the tasks across different runs. We present an open source toolbox for the implementation of multi-task batteries, along with a library containing group-averaged activity patterns that can be used to optimize battery selection for different brain structures of interest.

neuroscience↗

Multi-task fMRI outperforms resting-state fMRI for revealing task-invariant organization of the human brain

Resting-state functional Magnetic Resonance Imaging (fMRI) is widely used to infer the intrinsic functional organization of the brain, yet it remains unclear how well this approach can predict the structure of brain activity observed across a diverse set of mental states. Here we compare resting-state to task-based fMRI using diverse task batteries within the same individuals. We find that multi-task fMRI data consistently outperform resting-state estimates in predicting functional organization during novel tasks. This advantage persists across preprocessing strategies, brain regions, and independent datasets. While task activation estimates do show task-dependency when using only few tasks, increasing task diversity reduced task-specific bias, with convergence achieved using modest task sets. These improvements translate into superior individual parcellations and connectivity models. Together, our results dissociate reliability from validity in neuroimaging and challenge the prevailing assumption that rest provides a privileged window into intrinsic brain organization. Instead, functional architecture appears most faithfully revealed when the brain is actively driven through diverse task states.

neuroscience↗

Task-specific topographical maps of neural activity in the primate lateral prefrontal cortex

Neurons in the primate lateral prefrontal cortex (LPFC) flexibly adapt their activity to support a wide range of cognitive tasks. Whether and how the topography of LPFC neural activity changes as a function of task is unclear. In the present study, we address this issue by characterizing the functional topography of LPFC neural activity in awake behaving macaques performing three distinct cognitive tasks. We recorded from chronically implanted multi-electrode arrays and show that the topography of LPFC activity is stable within a task, but adaptive across tasks. The topography of neural activity exhibits a spatial scale compatible with prior anatomical tracing work on a!erent LPFC inputs. Our findings show that LPFC maps of neural population activity are stable for a specific task, providing robust neural codes that support task specialization. Moreover, the variability in functional topographies across tasks indicates activity landscapes can adapt, providing flexibility to LPFC neural codes.

neuroscience↗