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Maedbh King

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2 papers
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2

YNIMG Journal 2022 Journal Article

Predicting brain activation maps for arbitrary tasks with cognitive encoding models

  • Jonathon Walters
  • Maedbh King
  • Patrick G. Bissett
  • Richard B. Ivry
  • Jörn Diedrichsen
  • Russell A. Poldrack

A deep understanding of the neural architecture of mental function should enable the accurate prediction of a specific pattern of brain activity for any psychological task, based only on the cognitive functions known to be engaged by that task. Encoding models (EMs), which predict neural responses from known features (e.g., stimulus properties), have succeeded in circumscribed domains (e.g., visual neuroscience), but implementing domain-general EMs that predict brain-wide activity for arbitrary tasks has been limited mainly by availability of datasets that 1) sufficiently span a large space of psychological functions, and 2) are sufficiently annotated with such functions to allow robust EM specification. We examine the use of EMs based on a formal specification of psychological function, to predict cortical activation patterns across a broad range of tasks. We utilized the Multi-Domain Task Battery, a dataset in which 24 subjects completed 32 ten-minute fMRI scans, switching tasks every 35 s and engaging in 44 total conditions of diverse psychological manipulations. Conditions were annotated by a group of experts using the Cognitive Atlas ontology to identify putatively engaged functions, and region-wise cognitive EMs (CEMs) were fit, for individual subjects, on neocortical responses. We found that CEMs predicted cortical activation maps of held-out tasks with high accuracy, outperforming a permutation-based null model while approaching the noise ceiling of the data, without being driven solely by either cognitive or perceptual-motor features. Hierarchical clustering on the similarity structure of CEM generalization errors revealed relationships amongst psychological functions. Spatial distributions of feature importances systematically overlapped with large-scale resting-state functional networks (RSNs), supporting the hypothesis of functional specialization within RSNs while grounding their function in an interpretable data-driven manner. Our implementation and validation of CEMs provides a proof of principle for the utility of formal ontologies in cognitive neuroscience and motivates the use of CEMs in the further testing of cognitive theories.

YNICL Journal 2018 Journal Article

Unique degeneration signatures in the cerebellar cortex for spinocerebellar ataxias 2, 3, and 7

  • Carlos R. Hernandez-Castillo
  • Maedbh King
  • Jörn Diedrichsen
  • Juan Fernandez-Ruiz

Spinocerebellar ataxias (SCAs) are a heterogeneous group of neurodegenerative diseases that selectively affect vulnerable neuronal populations in the cerebellum and other subcortical regions. While previous studies have reported subtype differences in the absolute amount of degeneration in specific regions of interest, they failed to account for two important factors. First, they did not control for overall differences in the severity of the degeneration pattern, and second, they did not fully characterize the spatial pattern of degeneration for each SCA subtype. Here, we provide a systematic characterization of the spatial degeneration patterns for three polyQ SCAs (55 patients, either SCA2, SCA3, or SCA7) while controlling for the severity of the degeneration pattern. After this correction, the cerebellar degeneration pattern can successfully classify between the three different SCA subtypes with high cross-validated accuracy. Specifically, degeneration in SCA3 disproportionally affects motor regions of the cerebellar cortex, which explains the relatively severe motor symptoms observed in this subtype. Our results demonstrate that each of the three studied SCA subtypes has a unique cerebellar degeneration signature, hinting at differences in the disease process. Clinically, these differentiable patterns of cerebellar degeneration can be used to reliably discern subtypes, even at relatively early stages of the disease.

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