At the end of the first part, we stated that spatial coding is a certain spatial relation between the small volumes of the brain, and we asked whether one can find shared spatial coding in the brain areas for the given stimulus.
For example, if faces are presented to a subject in the fMRI scanner, one could expect a similar spatial relationship between the occipital cortex where visual information arrives and face-specific brain areas (e.g., the fusiform cortex, the orbitofrontal cortex).
To explore this issue, one needs to take a 3D pattern of the occipital cortex activity during face perception and compare it with other areas in the brain cortex.

To ensure that the observed activity is face-specific, one must compare face perception and a non-specific visual perception like images of totally degraded faces. This contrast image would be the mean difference between many presentations of faces and degraded faces.
However, there is a catch. If one takes a cube at the peak of the face-specific occipital activity, there is no sense in just moving it upwards-backward or in the anterior-posterior directions and comparing it with other parts of the cortex. The brain cortex is curved. It means that we should not only move the initial cube while comparing it with other areas of the cortex but also to rotate it. Testing various rotations can permit us to find the most appropriate orientation of the initial cube, which gives the highest correlation with activity at the given site.

The initial cube of activity is called a seed pattern. We applied the following steps of analysis using a seed pattern:
- The seed pattern (10x10x10 voxels) is centered on each voxel in the brain.
- Rotations around the X, Y, and Z axes with a step of 10 degrees, testing all possible combinations of rotations around the axes.
- The maximum correlation among all pattern rotations is selected and saved.
As a result of these manipulations, we obtained the 3D image, in which each voxel contained the maximum correlation among the rotations of the seed pattern centered at this voxel.
Such an image was obtained for each subject and statistical analysis of the group of subjects revealed statistically significant correlations (with correlation coefficients 0.5-0.8) in the contralateral occipital cortex and in face-specific regions:

Similarly, in the images of auditory word perception (contrasted with a non-specific auditory baseline), when we took the seed in the left auditory cortex, we found statistically significant correlations at the group level in the vicinity of this pattern and in the contralateral auditory cortex.

Given that we performed thousands of correlations per voxel with the rotated seed, we verified whether significant correlations could be obtained in a group of subjects just by chance. In the groups of subjects formed by randomized brain activity, no correlations were statistically significant. It means that there is a stimulus-specific overlap between the subjects in the areas correlated with the seed pattern. Thus, spatial coding is shared between the involved brain areas and is stimulus-specific.
Our method of rotational cross-correlations can be applied to functional brain images and structural ones. For example, we applied it to the PET image of amyloid plaques in a patient with Alzheimer’s disease. Placing the seed in the occipital cortex, one can see that at the correlation threshold of 0.5, similar spatial distributions of amyloid are observed in the temporal and paracingulate cortex. The diagnostic value of this approach presents a clinical perspective.

Of course, applications of the method to functional neuroimaging are also an interesting perspective for clinical research. For example, one can explore patterns of auditory activity in patients with asymmetric hearing loss. One can predict that the contralateral distribution of auditory activity in hearing loss (anacusis) is different from normal hearing listeners (NHL). Some hints for this can be found in the recent study of our group using classical neuroimaging analysis:

Sadoun A, Chauhan T, Mameri S, Zhang YF, Barone P, Deguine O, Strelnikov K. (2020) Stimulus-specific information is represented as local activity patterns across the brain. NeuroImage.



















