SENSE factors for reliable cortical thickness measurement.

The purposes of this study were to examine the effect of sensitivity encoding (SENSE) factors on cortical thickness measurements and to determine which SENSE factor to use to reliably measure cortical thickness in 3.0 T and 1.5 T T1-weighted MRI images. The 3D T1-TFE images were acquired from 11 healthy volunteers with 6 different SENSE acceleration factors from 1.0 (without SENSE acceleration) to 4.0 on a 1.5 T scanner, and 9 different SENSE factors from 1.0 to 6.0, plus a second-day 1.0 acquisition on a 3.0 T scanner. Cortical thickness was calculated for the entire cortical surface that was further subdivided into 33 regions. Repeated measures multivariate analysis of variance revealed that the main effect of SENSE factors (F=12.485, df=7, p=0.006) was a significant underestimation of cortical thickness at SENSE 5.0 (p=0.022) and 6.0 (p=0.011) at 3.0 T and at SENSE 4.0 (p<0.000) at 1.5 T. Repeated measures ANOVA showed that thickness measurements at the insula, superior temporal sulcus, the medial part of the superior frontal lobe, and cingulate cortex are highly affected by SENSE factors. SENSE factors affect thickness estimation more significantly at 1.5 T and thus 1.5 T imaging provides less reliable estimates using SENSE techniques. Faster imaging can be done without too much loss of reliability using a high SENSE factor, such as 3.0, at 3.0 T with acquisition time being inversely proportional to the SENSE factor.

Reorganization of neural circuits in the blind on diffusion direction analysis.

The neural reorganization of the visual cortex of early blind individuals was evaluated using voxel-by-voxel analysis of diffusion tensor images with regard to the diffusion direction, diffusion anisotropy and diffusivity. Reduced anisotropy and increased diffusivity was found mainly in the visual pathways of 18 early blind individuals as opposed to 25 sighted individuals. Alteration of the diffusion direction was detected not only in the visual pathways but also in nonvisual pathways such as the u fibers of the parietal lobe, the sagittal striatum, the pulvinar and the inferior and superior longitudinal fasciculi. The alteration of regional diffusion direction, reduced anisotropy and increased diffusivity in early blind individuals imply the neural reorganization for functional adaptation to the loss of visual input during the early development period.

Effects of active navigation on object recognition in virtual environments.

We investigated the importance and efficiency of active and passive exploration on the recognition of objects in a variety of virtual environments (VEs). In this study, 54 participants were randomly allocated into one of active and passive navigation conditions. Active navigation was performed by allowing participants to self-pace and control their own navigation, but passive navigation was conducted by forced navigation. After navigating VEs, participants were asked to recognize the objects that had been in the VEs. Active navigation condition had a significantly higher percentage of hit responses (t (52) = 4.000, p < 0.01), and a significantly lower percentage of miss responses (t (52) = -3.763, p < 0.01) in object recognition than the passive condition. These results suggest that active navigation plays an important role in spatial cognition as well as providing an explanation for the efficiency of learning in a 3D-based program.

Diffusion tensor MR imaging visualizes the altered hemispheric fiber connection in callosal dysgenesis.

We report three cases of callosal dysgenesis that were evaluated by diffusion tensor imaging and fiber tractography. In partial agenesis of corpus callosum, fiber tracts from all regions of brain converged to a partially developed small genu portion and connected to the contralateral side. In complete callosal agenesis, fibers from the hemispheres failed to cross the midline and formed thick bundles running anteroposteriorly (eg, Probst bundle). The thickness of the anterior commissure was enlarged or smaller than normal brain, and other white matter tracts were not markedly different from normal brain tissue.

Diffusion tensor MRI and fiber tractography of cerebellar atrophy in phenytoin users.

PURPOSE: The usefulness of diffusion tensor magnetic resonance imaging (DT-MRI) is still in debate, and the development of clinically feasible scan protocol is encouraged. The purpose of this study was to investigate the afferent fiber system to the cerebellum in patients with phenytoin (PHT)-induced cerebellar atrophy in comparison with cerebellar atrophy of other etiologies by using DT-MRI. METHODS: Thirteen patients (M/F ratio, 7:6; mean age, 42.5 years) and age-matched normal controls (n = 8) participated in this study. The patient group consisted of epilepsy patients who had received PHT therapy (n = 9) and clinically diagnosed as having olivopontocerebellar atrophy (OPCA; n = 4). DT-MRI was performed by using diffusion weighting of b = 600 s/mm2, and fractional anisotropy (FA) and color-coded vector maps were generated. FA of the middle cerebellar peduncle (MCP), the cerebellum, and transverse pontine fibers (TPF) was measured and compared between PHT and OPCA patients. RESULTS: Normal subjects showed FA values of 0.81 +/- 0.07 in MCP, 0.69 +/- 0.04 in TPF, and PHT users showed FA values of 0.84 +/- 0.09 in MCP, 0.72 +/- 0.08 in TPF, and 0.21 +/- 0.04 in cerebellum. OPCA patients showed FA values of 0.39 +/- 0.11 in MCP, 0.46 +/- 0.12 in TPF, and 0.22 +/- 0.07 in cerebellum. PHT users showed a statistically significant reduction of FA only in cerebellum, whereas OPCA demonstrated significant decrease of FA in MCP, TPF, and cerebellum (one-way analysis of variance, p < 0.01). Three-dimensional reconstruction of fiber tracts demonstrated decreased volume and altered fiber integrity within the peduncles and transverse pontine fibers in the OPCA group, whereas fiber course patterns in PHT users were similar to those in controls. CONCLUSIONS: PHT users showed normal orientation and anisotropy of MCP and TPF, whereas OPCA demonstrated impaired values, suggesting that PHT directly affects the cerebellum. DT-MRI can demonstrate detailed fiber configurations in degenerative diseases of brainstem and cerebellum and provides insight into the pathomechanisms of cerebellar atrophy.