September 2024
Volume 24, Issue 10
Open Access
Vision Sciences Society Annual Meeting Abstract  |   September 2024
Dynamic functional connectivity via iEEG - fMRI correlation maps
Author Affiliations & Notes
  • Zeeshan Qadir
    Mayo Clinic
  • Harvey Huang
    Mayo Clinic
  • Morgan Montoya
    Mayo Clinic
  • Michael Jensen
    Mayo Clinic
  • Gabriela Ojeda Valencia
    Mayo Clinic
  • Kai Miller
    Mayo Clinic
  • Gregory Worrell
    Mayo Clinic
  • Thomas Naselaris
    University of Minnesota
  • Kendrick Kay
    Department of Psychology York University, Toronto, ON, Canada
  • Dora Hermes
    Mayo Clinic
  • Footnotes
    Acknowledgements  We thank the patients in this study for their participation, Cindy Nelson and Karla Crockett for their assistance, and Peter Brunner for support with BCI2000. Research reported in this publication was supported by the NEI (R01EY035533, R01EY023384)
Journal of Vision September 2024, Vol.24, 1304. doi:https://doi.org/10.1167/jov.24.10.1304
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      Zeeshan Qadir, Harvey Huang, Morgan Montoya, Michael Jensen, Gabriela Ojeda Valencia, Kai Miller, Gregory Worrell, Thomas Naselaris, Kendrick Kay, Dora Hermes; Dynamic functional connectivity via iEEG - fMRI correlation maps. Journal of Vision 2024;24(10):1304. https://doi.org/10.1167/jov.24.10.1304.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Understanding neural computations of vision require studying how different brain regions interact with one another. However, functional connectivity across brain regions is often computed as stationary maps, concealing the rich neural dynamics that change at a finer timescale. To better understand how functional connectivity evolves over time, we propose a multimodal framework combining data from intracranial-EEG (iEEG) and fMRI. We recorded iEEG data from early visual (V1/V2) electrodes in 4 patients. Each patient was shown a subset of 1000 stimuli from the NSD-fMRI dataset. Electrodes with significant broadband (70-170 Hz) power increases w.r.t the baseline were considered for further analysis. From the NSD-fMRI dataset, we obtained average fMRI beta-weights for the 1000 stimuli that were repeated thrice across the 8 subjects. Next, for each iEEG electrode we computed a Pearson correlation map with all the fMRI vertices, across the 1000 stimuli, giving us a time x vertices correlation matrix. This provided us with a brain-wide temporally evolving correlation map for each electrode. In all 4 subjects, we observed that the iEEG broadband significantly correlates with the fMRI beta-weights in V1, and with V2/V3 about 5-10 ms later, followed by the ventral temporal regions around 170 ms. Other parietal and frontal brain regions also showed significant correlations after 100 ms. Further, we also observed that these correlations reduce around 450 ms, even though the stimuli were presented for 800 ms. These temporally resolved correlation maps show that V1 representations are not stationary but share representations with higher order visual areas over time. These results may suggest that connectivity to V1 evolves over time revealing feedback inputs from higher order ventral areas around 100-170 ms. Overall, we propose that our multimodal framework enables us to compute functional connectivity at high spatiotemporal resolution reflecting the rich dynamics of interaction across different brain regions.

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