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Neuropsychiatric symptoms in genetic frontotemporal dementia: developing a new module for Clinical Rating Scales

Abstract:
Background: Current clinical rating scales in frontotemporal dementia (FTD) often do not incorporate neuropsychiatric features and may therefore inadequately measure disease stage. Methods: 832 participants from the Genetic FTD Initiative (GENFI) were recruited: 522 mutation carriers and 310 mutation-negative controls. The standardised GENFI clinical questionnaire assessed the frequency and severity of 14 neuropsychiatric symptoms: visual, auditory, and tactile hallucinations, delusions, depression, anxiety, irritability/lability, agitation/aggression, euphoria/elation, aberrant motor behaviour, hypersexuality, hyperreligiosity, impaired sleep, and altered sense of humour. A principal component analysis (PCA) was performed to identify key groupings of neuropsychiatric and behavioural items in order to create a new neuropsychiatric module that could be used as an addition to the Clinical Dementia Rating (CDR) plus National Alzheimer's Coordinating Center Behaviour and Language Domains (NACC FTLD) rating scale. Results: Overall, 46.4% of mutation carriers had neuropsychiatric symptoms (51.6% C9orf72, 40.8% GRN, 46.6% MAPT) compared with 24.5% of controls. Anxiety and depression were the most common in all genetic groups but fluctuated longitudinally and loaded separately in the PCA. Hallucinations and delusions loaded together, with the remaining neuropsychiatric symptoms loading with the core behavioural features of FTD. These results suggest using a single 'psychosis' neuropsychiatric module consisting of hallucinations and delusions. Adding this to the CDR plus NACC FTLD, called the CDR plus NACC FTLD-N, leads to a number of participants being scored more severely, including those who were previously considered asymptomatic now being scored as prodromal. Conclusions: Neuropsychiatric symptoms occur in mutation carriers at all disease stages across all three genetic groups. However, only psychosis features provided additional staging benefit to the CDR plus NACC FTLD. Inclusion of these features brings us closer to optimising the rating scale for use in trials
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1136/jnnp-2022-330152
Publication website:
https://arts.units.it/bitstream/11368/3097157/3/357.full.pdf

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Author
ORCID:
0000-0002-3105-7099
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Role:
Author
ORCID:
0000-0002-2900-9602
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Role:
Author
ORCID:
0000-0002-3319-138X
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Author
ORCID:
0000-0002-0267-8590
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Role:
Author
ORCID:
0000-0003-1814-5024


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Funder identifier:
10.13039/501100017510
Grant:
SM-UCLO-MA-0519
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Funder identifier:
10.13039/501100004047
Grant:
Doctoral Funding
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Funder identifier:
10.13039/501100001320
Grant:
n/a
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Funder identifier:
10.13039/100010269
Grant:
103838
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Funder identifier:
10.13039/501100000320
Grant:
AS-JF-19a-004-517


Publisher:
BMJ Publishing Group
Journal:
Journal of Neurology, Neurosurgery and Psychiatry More from this journal
Volume:
94
Issue:
5
Pages:
357-368
Publication date:
2023-01-10
DOI:
EISSN:
1468-330X
ISSN:
0022-3050


Language:
English
Keywords:
Pubs id:
1345685
Local pid:
pubs:1345685
Source identifiers:
W4314935516
Deposit date:
2026-05-08
ARK identifier:
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