Mapping behavioural, cognitive and affective transdiagnostic dimensions in frontotemporal dementia

Author:

Ramanan Siddharth123,El-Omar Hashim2,Roquet Daniel23,Ahmed Rebekah M24ORCID,Hodges John R235,Piguet Olivier23ORCID,Lambon Ralph Matthew A1ORCID,Irish Muireann23ORCID

Affiliation:

1. Medical Research Council Cognition and Brain Sciences Unit, The University of Cambridge , Cambridge CB3 1AU , UK

2. Brain and Mind Centre, The University of Sydney , Sydney, NSW 2050 , Australia

3. School of Psychology, The University of Sydney , Sydney, NSW 2050 , Australia

4. Memory and Cognition Clinic, Department of Clinical Neurosciences, Royal Prince Alfred Hospital , Sydney, NSW 2050 , Australia

5. School of Medical Sciences, The University of Sydney , Sydney, NSW 2050 , Australia

Abstract

Abstract Two common clinical variants of frontotemporal dementia are the behavioural variant frontotemporal dementia, presenting with behavioural and personality changes attributable to prefrontal atrophy, and semantic dementia, displaying early semantic dysfunction primarily due to anterior temporal degeneration. Despite representing independent diagnostic entities, mounting evidence indicates overlapping cognitive–behavioural profiles in these syndromes, particularly with disease progression. Why such overlap occurs remains unclear. Understanding the nature of this overlap, however, is essential to improve early diagnosis, characterization and management of those affected. Here, we explored common cognitive–behavioural and neural mechanisms contributing to heterogeneous frontotemporal dementia presentations, irrespective of clinical diagnosis. This transdiagnostic approach allowed us to ascertain whether symptoms not currently considered core to these two syndromes are present in a significant proportion of cases and to explore the neural basis of clinical heterogeneity. Sixty-two frontotemporal dementia patients (31 behavioural variant frontotemporal dementia and 31 semantic dementia) underwent comprehensive neuropsychological, behavioural and structural neuroimaging assessments. Orthogonally rotated principal component analysis of neuropsychological and behavioural data uncovered eight statistically independent factors explaining the majority of cognitive–behavioural performance variation in behavioural variant frontotemporal dementia and semantic dementia. These factors included Behavioural changes, Semantic dysfunction, General Cognition, Executive function, Initiation, Disinhibition, Visuospatial function and Affective changes. Marked individual-level overlap between behavioural variant frontotemporal dementia and semantic dementia was evident on the Behavioural changes, General Cognition, Initiation, Disinhibition and Affective changes factors. Compared to behavioural variant frontotemporal dementia, semantic dementia patients displayed disproportionate impairment on the Semantic dysfunction factor, whereas greater impairment on Executive and Visuospatial function factors was noted in behavioural variant frontotemporal dementia. Both patient groups showed comparable magnitude of atrophy to frontal regions, whereas severe temporal lobe atrophy was characteristic of semantic dementia. Whole-brain voxel-based morphometry correlations with emergent factors revealed associations between fronto-insular and striatal grey matter changes with Behavioural, Executive and Initiation factor performance, bilateral temporal atrophy with Semantic dysfunction factor scores, parietal-subcortical regions with General Cognitive performance and ventral temporal atrophy associated with Visuospatial factor scores. Together, these findings indicate that cognitive–behavioural overlap (i) occurs systematically in frontotemporal dementia; (ii) varies in a graded manner between individuals and (iii) is associated with degeneration of different neural systems. Our findings suggest that phenotypic heterogeneity in frontotemporal dementia syndromes can be captured along continuous, multidimensional spectra of cognitive–behavioural changes. This has implications for the diagnosis of both syndromes amidst overlapping features as well as the design of symptomatic treatments applicable to multiple syndromes.

Funder

Forefront

National Health and Medical Research Council

Australia program

Australian Research Council

Centre of Excellence in Cognition and its Disorders Memory Program

NHMRC Senior Research Fellowship

ARC Future Fellowship

ARC Discovery Project

United Kingdom Research and Innovation–Medical Research Council

European Research Council

Publisher

Oxford University Press (OUP)

Subject

Neurology,Cellular and Molecular Neuroscience,Biological Psychiatry,Psychiatry and Mental health

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