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Neuroanatomical correlates of apathy and disinhibition, behavioral abnormalities in behavioral variant Frontotemporal dementia (bvFTD) remain unclear. In this study 45 participants (25 bvFTD patients and 20 controls) provided data on clinical, neuropsychological, behavioral (on Frontal Systems Behavior (FrSBe) Scale), cortical volume (on voxel-based morphometry (VBM)) and tract based spatial fractional anisotropy ((FA) on magnetic resonance imaging (MRI), allowing examination of the neural correlates of apathy and disinhibition. The patients with bvFTD had predominant grey matter loss and corresponding white matter fractional anisotropy reduction in the frontal and temporal lobe compared to the controls. Grey matter loss in frontal, temporal and limbic structures correlated with apathy and degeneration in temporal limbic brain areas correlated with disinhibition. FA changes in inferior fronto-occipital fasciculus and forceps minor correlated with apathy and fibre integrity changes in the superior longitudinal fasciculus correlated with disinhibition. The current study suggests that apathy and disinhibition arises due to changes in the frontal, temporal and limbic brain areas in bvFTD. [ABSTRACT FROM AUTHOR]

Fractal dimension (FD) is a quantitative parameter that can characterizes the complexity of human brain tissue. Extensive grey matter (GM) pathology has been previously identified in Frontotemporal dementia (FTD) and its variants. The aim of the present study was to investigate the GM morphometric abnormalities in the behavioral variant FTD (bvFTD) and primary progressive aphasia (PPA) using FD analysis. Twenty-seven bvFTD, 12 PPA and 20 controls were studied. SPM8 was used to segment the brain into GM tissue. Then the FD values were estimated for the GM skeleton, surface and general structure in patients and controls using our previously published algorithm. We found that patients with bvFTD had significant reduction in FD values of skeleton and general structure when compared to controls. In PPA, more significant decrease in FD was noted in the whole brain and left hemisphere skeleton along with left hemisphere general structure. Only the right hemisphere skeleton had a significant correlation with total score of Frontal Systems Behavior Scale (FrSBe). The results showed that the variants of FTD are associated with disease specific morphometric complexity patterns. These results indicate that FD can be used as a biomarker for the structural changes associated with neurodegenerative diseases. [ABSTRACT FROM AUTHOR]