Abstract

Behavioural disturbances in frontotemporal dementia (FTD) are thought to reflect mainly atrophy of cortical regions. Recent studies suggest that subcortical brain regions, in particular the striatum, are also significantly affected and this pathology might play a role in the generation of behavioural symptoms.OBJECTIVETo investigate prefrontal cortical and striatal atrophy contributions to behavioural symptoms in FTD.METHODSOne hundred and eighty-two participants (87 FTD patients, 39 AD patients and 56 controls) were included. Behavioural profiles were established using the Cambridge Behavioural Inventory Revised (CBI-R) and Frontal System Behaviour Scale (FrSBe). Atrophy in prefrontal (VMPFC, DLPFC) and striatal (caudate, putamen) regions was established via a 5-point visual rating scale of the MRI scans. Behavioural scores were correlated with atrophy rating scores.RESULTSBehavioural and atrophy ratings demonstrated that patients were significantly impaired compared to controls, with bvFTD being most severely affected. Behavioural-anatomical correlations revealed that VMPFC atrophy was closely related to abnormal behaviour and motivation disturbances. Stereotypical behaviours were associated with both VMPFC and striatal atrophy. By contrast, disturbance of eating was found to be related to striatal atrophy only.CONCLUSIONFrontal and striatal atrophy contributed to the behavioural disturbances seen in FTD, with some behaviours related to frontal, striatal or combined fronto-striatal pathology. Consideration of striatal contributions to the generation of behavioural disturbances should be taken into account when assessing patients with potential FTD.

Highlights

  • Frontotemporal dementia (FTD) can be divided into three clinical subtypes: behavioural frontotemporal dementia, semantic dementia (SD) and progressive non-fluent aphasia (PNFA)

  • Post-hoc analysis showed that behavioural frontotemporal dementia (bvFTD) patients and controls differed from each other (p

  • Our findings suggest that cortical and striatal pathology in FTD may have differential roles in the genesis of the behavioural symptoms which characterise FTD

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Summary

Introduction

Frontotemporal dementia (FTD) can be divided into three clinical subtypes: behavioural frontotemporal dementia (bvFTD), semantic dementia (SD) and progressive non-fluent aphasia (PNFA). Basal ganglia degeneration was very evident as indicated by grossly dilated frontal horns of the lateral ventricles. These pathological findings were confirmed in vivo[10,11,12,13] using MRI volumetrics demonstrating striatal atrophy especially in those with bvFTD and PNFA.[11,13,14]

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