A novel, direct spatio-temporal approach for analyzing fMRI experiments

  • Authors:
  • R. L. Somorjai;R. Vivanco;N. Pizzi

  • Affiliations:
  • Institute for Biodiagnostics, National Research Council Canada, 435 Ellice Avenue, Winnipeg MB, Canada R3B 1Y6;Institute for Biodiagnostics, National Research Council Canada, 435 Ellice Avenue, Winnipeg MB, Canada R3B 1Y6;Institute for Biodiagnostics, National Research Council Canada, 435 Ellice Avenue, Winnipeg MB, Canada R3B 1Y6

  • Venue:
  • Artificial Intelligence in Medicine
  • Year:
  • 2002

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Abstract

We introduce a novel approach to couple temporal similarity with spatial neighborhood information. This is achieved by concatenating the K nearest, spatially contiguous neighbors of a pixel time-course (TC) of T time-instances. This produces a new TC of (K+1)T time instances. Depending on how ''nearest'' is defined, we have various options. Strictly spatial nearness means augmenting a given TC by its K nearest neighbors in some canonical spatial order. A more powerful and flexible option is to order the TCs to be concatenated according to their temporal similarity to the central voxel TC. For this study, we have chosen Pearson's cross-correlation coefficient as the measure of similarity. For more than a single neighbor, two concatenation options are possible. The direct ordering option requires that the TCs to be concatenated be spatially contiguous to the central pixel. The more flexible indirect option merely demands that one of a chain of temporally similar TCs be spatially connected to the central pixel. We also apply the temporal similarity criterion to the more conventional spatial (median) filtering, and show that it gives superior result to a strict spatial filtering. The method is tested and verified on a null fMRI dataset onto which we superposed two types of ''activations'' with known temporal behavior and spatial location. It is also applied to a real dataset containing visual activation. We also propose a strategy, based on the flexibility of the method, to determine a consensus, ''core'' set of activations.