(i) GLM |
(ii) PARAFAC |
The results for GLM are shown in figure 8(i) (all maps are shown in neurological convention, i.e. left hemisphere is displayed on the left). Similar to the thresholded -stat maps presented in the original paper by [McGonigle et al., 2000], the super-thresholded clusters coincide with areas typically involved in motor processing: bilateral premotor, contra-lateral primary motor and sensory areas, SMA, bilateral secondary somatosensory and the ipsilateral anterior lobe of the cerebellum. Based on the Gaussian/Gamma mixture model fit, significantly negative group-level -scores are found in ipsilateral primary motor areas, bilateral intra-parietal sulcus and occipital parietal cortex (blue). Below the GLM map is the first-level GLM regressor together with its power spectrum. Also shown is the normalised (to unit standard deviation) set of first level parameter estimates, weighted by the group-level -scores and averaged within post-threshold group-level activation clusters. At the group level, the averaged and weighted set of first-level estimates expresses the change in effect 'strength' between different sessions similar to what is estimated explicitly as part of the PARAFAC and tensor-PICA decomposition as the third mode, (see [Smith et al., 2004] for examples of the usefulness of this quantity in the context of model-based FMRI group analysis).
The main PARAFAC map8 in figure 8(ii) similarly shows super-thresholded clusters in premotor and motor areas, but shows fewer voxels in secondary somatosensory areas and does not identify an ipsilateral cluster in the cerebellar cortex. The power spectrum of the associated time course has highest power at the fundamental frequency of the design (6.5 cycles) but also large power at the first harmonic and some higher frequencies.
By comparison, the primary tensor-PICA map (figure 9(i)) shows much larger correlation with the GLM map than the main PARAFAC map. The spatial map from tensor-PICA shows areas similar to the GLM mixed-effects map, with the tensor-PICA map more prominently showing clusters in bilateral secondary somatosensory (S2) areas. Additionally, cingulate motor and ipsilateral primary motor areas have survived thresholding. Among the 19 estimated sources, this process has not only the highest spatial correlation with the GLM map, but also the highest temporal correlation with the GLM design and highest mean effect size. The rank-1 approximation explains of the variation between the temporal responses for each of the sessions. Similar to the PARAFAC results, there is some correspondence between the normalised9 estimated session response (bottom) and the weighted averaged GLM first-level parameter estimates (figure 8(i), bottom).
(i) primary tensor-PICA map |
(ii) secondary tensor-PICA map |
The ''negative'' activation in the GLM map (e.g. ipsilateral motor areas) no longer shows up in this map but is contained within a separate tensor-PICA map10 shown in figure 10(ii). The most strongly de-activated areas include the ipsilateral primary motor areas and somatosensory areas, possibly de-activating 'non-hand' motor areas as shown previously for the somatosensory system [Drevets et al., 1995]. The plot of the normalised response size over sessions does show that this de-activation is consistent over sessions. The amount of explained variance in the rank-1 approximation , however, is reduced to , suggesting that, unlike primary activation, the de-activation is less consistent in the temporal characteristics between sessions.
Some parts of the de-activation as identified in the GLM analysis (blue in figure (i)), however, do not appear in the primary de-activation map shown in figure 9(ii). Instead, a third tensor-PICA map (with correlation of to the GLM design) shows de-activation in the superior occipital lobule, an area commonly involved in stereo vision (see figure 10). Unlike the de-activation depicted in figure 9(ii), only a few of the 10 sessions show a significantly non-zero effect size: the boxplot shows sessions 8 and 10 as 'outliers', possibly due to visual fixation.
Similar to the case of the artificial data, figure 11 demonstrates that the tensor-PICA results show a much clearer identification of a single ``activation'' map as well as reduced cross-talk between estimated maps.
Additional 'interesting' maps from the tensor-PICA decomposition are shown in figure 12: the first map (i) depicts the spatial extent of an image artefact showing signal fluctuations possibly due to RF signal aliased into the field-of-view. While the exact origin of these signal components is unknown, they negatively impact on a group GLM analysis as these pattern induce additonal error variance. Figure 12(ii) shows stimulus-correlated residual head motion, most clearly appearing at the frontal lobe intensity boundaries. The presence of this artefact strongly impacts on standard GLM analysis: both the single-level (for session 6) and the group-level GLM estimates for motor activation show false positives around the area where the tensor-PICA map shows the residual motion. Though only a few sessions are estimated to contain this spatio-temporal process, the amplitude modulation induced by the artefacts within these sessions is large enough to be significant even at the group level.