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A Bayesian General Linear Modeling Approach to Cortical Surface fMRI Data Analysis

Version 5 2023-08-16, 17:22
Version 4 2021-09-15, 14:24
Version 3 2019-12-09, 13:40
Version 2 2019-06-12, 13:33
Version 1 2019-05-02, 17:08
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posted on 2023-08-16, 17:22 authored by Amanda F. Mejia, Yu (Ryan) Yue, David Bolin, Finn Lindgren, Martin A. Lindquist

Cortical surface functional magnetic resonance imaging (cs-fMRI) has recently grown in popularity versus traditional volumetric fMRI. In addition to offering better whole-brain visualization, dimension reduction, removal of extraneous tissue types, and improved alignment of cortical areas across subjects, it is also more compatible with common assumptions of Bayesian spatial models. However, as no spatial Bayesian model has been proposed for cs-fMRI data, most analyses continue to employ the classical general linear model (GLM), a “massive univariate” approach. Here, we propose a spatial Bayesian GLM for cs-fMRI, which employs a class of sophisticated spatial processes to model latent activation fields. We make several advances compared with existing spatial Bayesian models for volumetric fMRI. First, we use integrated nested Laplacian approximations, a highly accurate and efficient Bayesian computation technique, rather than variational Bayes. To identify regions of activation, we utilize an excursions set method based on the joint posterior distribution of the latent fields, rather than the marginal distribution at each location. Finally, we propose the first multi-subject spatial Bayesian modeling approach, which addresses a major gap in the existing literature. The methods are very computationally advantageous and are validated through simulation studies and two task fMRI studies from the Human Connectome Project.

Supplementary materials for this article, including a standardized description of the materials available for reproducing the work, are available as an online supplement.

Funding

Data were provided in part by the Human Connectome Project, WU-Minn Consortium (Principal Investigators: David Van Essen and Kamil Ugurbil; 1U54MH091657) funded by the 16 NIH Institutes and Centers that support the NIH Blueprint for Neuroscience Research; and by the McDonnell Center for Systems Neuroscience at Washington University. This research was supported in part by NIH grants P41 EB015909, R01 EB016061 and R01 EB027119 from the National Institute of Biomedical Imaging and Bioengineering, PSC-CUNY Research Award 67192-00 45, and Swedish Research Council grant 2016-04187.

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