In vivo validation of simulated run-to-run variability in population receptive field estimations

Poster No:

2080 

Submission Type:

Abstract Submission 

Authors:

Siddharth Mittal1, Michael Woletz1, David Linhardt1, Christian Windischberger1

Institutions:

1Medical University of Vienna, Vienna, Austria

First Author:

Siddharth Mittal  
Medical University of Vienna
Vienna, Austria

Co-Author(s):

Michael Woletz  
Medical University of Vienna
Vienna, Austria
David Linhardt  
Medical University of Vienna
Vienna, Austria
Christian Windischberger  
Medical University of Vienna
Vienna, Austria

Introduction:

Population receptive field (pRF) mapping is a widely used approach in functional neuroimaging to analyze the relationship between visual field stimulation and neural activation in the visual cortex. Despite advancements in modelling, software, and stimulus design, significant run-to-run variability persists in estimated pRF parameters. This study used computational modelling to simulate variability across runs and validate results against in vivo variability observed in 30 empirical retinotopy runs.

Methods:

All computations were performed using our novel pRF mapping software GEM-pRF, which was designed to take full advantage of GPU acceleration in order to minimise computation time (Mittal et al., 2024). Empirical data was collected from a retinotopy experiment on a young healthy female subject across five sessions (six runs each, 30 runs total). A moving bar with a flickering checkerboard served as the stimulus. pRF estimations for each vertex were computed using GEM-pRF, yielding 30 pRF values per vertex based on a 2D isotropic Gaussian model, with parameters including spatial coordinates (μx, μy) and size (σ).

For simulations, receptive fields were uniformly distributed across 51×51 spatial locations (μx, μy) with varying sizes (σ). Using the same stimulus, 5000 simulated BOLD responses per location and size were generated with white noise, achieving a contrast-to-noise ratio (CNR) of 1 to 4. This dataset was processed using GEM-pRF, and the resulting parameters were used to estimate the probability distribution of pRF parameters for each ground-truth position. Maximum likelihood (ML) estimation matched simulated distributions to empirical voxel data. Multivariate Kolmogorov-Smirnov tests (Naaman, 2021) assessed differences between simulated and empirical distributions.

Results:

Empirical data showed that the estimations of pRF results across runs varied depending on the position in the visual field (μx, μy). Variability was lower in the foveal regions compared to the more peripheral areas. In particular, distributions in foveal regions were found circular and Gaussian-like, while peripheral locations exhibited ellipsoidal distributions with increased width along the eccentricity direction. Figure 1 illustrates a matching result for a foveal vertex, while Figure 2 represents the matching of a parafoveal vertex. Both figures highlight the scattering of estimated pRF parameters for a given vertex, overlaid on the KDE distribution of the matched simulated pRF. The matched KDEs of the parafoveal vertex (Figure 2) and the near-foveal region vertex (Figure 1) reveal distinct differences in parameter variability across the spatial dimensions (μx, μy​) and pRF size (σ). The parafoveal vertex exhibits broader spreads of 5.58, 6.3, and 1.95 for μx​, μy​, and σ, respectively, with corresponding standard deviations of 1.18, 1.47, and 0.57. The covariance matrix for the spatial domain (μx, μy​) of the parafoveal vertex yields eigenvalues of 0.153 and 3.395, confirming an elliptical distribution with greater variability along one axis. In contrast, the near-foveal vertex shows narrower spreads of 0.54, 0.72, and 0.788, and smaller standard deviations of 0.16, 0.16, and 0.25 for the same parameters. Its covariance matrix produces nearly equal eigenvalues of 0.025 and 0.025, supporting a circular distribution in the spatial domain. These findings suggest that the parafoveal vertex covers a larger and more variable parameter space, while the near-foveal vertex reflects a more constrained and isotropic representation.

Conclusions:

This study shows that run-to-run variability in empirical pRF estimates can be replicated with simulations. This validation opens up the door to examining intrinsic biases in pRF stimulus configurations, quantifying estimation efficiency for arbitrary visual stimulation patterns, and developing novel layouts to optimize pRF estimation experiments. As a result, pRF runs will become shorter and/or more reliable, benefiting clinical applications.
Supporting Image: 5000bmergedfiguresvg2024_12_17_15_52_180.png
   ·Fig. 1: Foveal vertex results showing empirical pRF distribution along with best-fit simulated data KDE (marginalized over sigma) and its ground truth spatial parameters (μx, μy).
Supporting Image: 394bmergedfiguresvg2024_12_17_15_52_180.png
   ·Fig. 2: Parafoveal vertex results showing empirical pRF distribution along with best-fit simulated data KDE (marginalized over sigma) and its ground truth spatial parameters (red dot).
 

Modeling and Analysis Methods:

Activation (eg. BOLD task-fMRI) 2

Perception, Attention and Motor Behavior:

Perception: Visual 1

Keywords:

Computational Neuroscience
Cortex
Data analysis
FUNCTIONAL MRI
Open-Source Code
Open-Source Software
Spatial Normalization

1|2Indicates the priority used for review

Abstract Information

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Please indicate below if your study was a "resting state" or "task-activation” study.

Task-activation

Healthy subjects only or patients (note that patient studies may also involve healthy subjects):

Healthy subjects

Was this research conducted in the United States?

No

Were any human subjects research approved by the relevant Institutional Review Board or ethics panel? NOTE: Any human subjects studies without IRB approval will be automatically rejected.

Yes

Were any animal research approved by the relevant IACUC or other animal research panel? NOTE: Any animal studies without IACUC approval will be automatically rejected.

Not applicable

Please indicate which methods were used in your research:

Functional MRI
Neurophysiology
Computational modeling

For human MRI, what field strength scanner do you use?

3.0T

Which processing packages did you use for your study?

Other, Please list  -   GEM-pRF

Provide references using APA citation style.

Mittal, S., Woletz, M., Linhardt, D., & Windischberger, C. (2024). A novel approach for population receptive field mapping using high-performance computing. Journal of Vision, 24(10), 536-536.

Naaman, M. (2021). On the tight constant in the multivariate Dvoretzky–Kiefer–Wolfowitz inequality. Statistics & Probability Letters, 173, 109088.

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