Evidence map›Paper›PMID 36811680›Full record

ArticleJournal of neurology2023

Addition of the FTD Module to the Neuropsychiatric Inventory improves classification of frontotemporal dementia spectrum disorders.

Lize C Jiskoot, Lucy L Russell, Caroline V Greaves, Esther van Schaik, Esther van den Berg, Jackie M Poos, Liset de Boer, Laura Donker Kaat, Harro Seelaar, Yolande A L Pijnenburg and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Caregiver perspectives enable accurate diagnosis of neurodegenerative disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  6. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 2 countries.

Lize C JiskootDepartment of Neurology and Alzheimer Center Erasmus MC, Erasmus MC University Medical Center, Room NF-331, Dr. Molenwaterplein 40, 3015 CE, Rotterdam, The Netherlands. l.c.jiskoot@erasmusmc.nl.ORCID http://orcid.org/0000-0002-1120-1858
Lucy L RussellDementia Research Centre, Department of Neurodegenerative Disease, University College London Queen Square Institute of Neurology, London, UK.
Caroline V GreavesDementia Research Centre, Department of Neurodegenerative Disease, University College London Queen Square Institute of Neurology, London, UK.
Esther van SchaikDepartment of Neurology and Alzheimer Center Erasmus MC, Erasmus MC University Medical Center, Room NF-331, Dr. Molenwaterplein 40, 3015 CE, Rotterdam, The Netherlands.
Esther van den BergDepartment of Neurology and Alzheimer Center Erasmus MC, Erasmus MC University Medical Center, Room NF-331, Dr. Molenwaterplein 40, 3015 CE, Rotterdam, The Netherlands.
Jackie M PoosDepartment of Neurology and Alzheimer Center Erasmus MC, Erasmus MC University Medical Center, Room NF-331, Dr. Molenwaterplein 40, 3015 CE, Rotterdam, The Netherlands.
Liset de BoerDepartment of Neurology and Alzheimer Center Erasmus MC, Erasmus MC University Medical Center, Room NF-331, Dr. Molenwaterplein 40, 3015 CE, Rotterdam, The Netherlands.
Laura Donker KaatDepartment of Neurology and Alzheimer Center Erasmus MC, Erasmus MC University Medical Center, Room NF-331, Dr. Molenwaterplein 40, 3015 CE, Rotterdam, The Netherlands.
Harro SeelaarDepartment of Neurology and Alzheimer Center Erasmus MC, Erasmus MC University Medical Center, Room NF-331, Dr. Molenwaterplein 40, 3015 CE, Rotterdam, The Netherlands.
Yolande A L PijnenburgDepartment of Neurology, Amsterdam University Medical Centre, Amsterdam, The Netherlands.
John C van SwietenDepartment of Neurology and Alzheimer Center Erasmus MC, Erasmus MC University Medical Center, Room NF-331, Dr. Molenwaterplein 40, 3015 CE, Rotterdam, The Netherlands.
Jonathan D RohrerDementia Research Centre, Department of Neurodegenerative Disease, University College London Queen Square Institute of Neurology, London, UK.
Erasmus MC · NLUK Dementia Research Institute · GBUniversity of Amsterdam · NL

Funding

Alzheimer Nederland WE.15-2019.02JPND GENFI-PROX grant 2019-02248JPND PreFrontAls Consortium 733051042Medical Research Council MR/M008525/1Medical Research Council MR/M023664/1Medical Research Council MR/T046015/1MRC Clinician Scientist Fellowship MR/M008525/1MRC UK GENFI grant MR/M023664/1NIHR Rare Disease Translational Research Collaboration BRC149/NS/MHNWO HCMI 056-13-018the Association for Frontotemporal Dementias Research 2009the Dioraphte Foundation 09-02-00ZonMw Memorabel 733050103ZonMw Memorabel 733050813
6 · The paper itself

Abstract

Most neuropsychiatric symptoms (NPS) common in frontotemporal dementia (FTD) are currently not part of the Neuropsychiatric Inventory (NPI). We piloted an FTD Module that included eight extra items to be used in conjunction with the NPI. Caregivers of patients with behavioural variant FTD (n = 49), primary progressive aphasia (PPA; n = 52), Alzheimer's dementia (AD; n = 41), psychiatric disorders (n = 18), presymptomatic mutation carriers (n = 58) and controls (n = 58) completed the NPI and FTD Module. We investigated (concurrent and construct) validity, factor structure and internal consistency of the NPI and FTD Module. We performed group comparisons on item prevalence, mean item and total NPI and NPI with FTD Module scores, and multinomial logistic regression to determine its classification abilities. We extracted four components, together explaining 64.1% of the total variance, of which the largest indicated the underlying dimension 'frontal-behavioural symptoms'. Whilst apathy (original NPI) occurred most frequently in AD, logopenic and non-fluent variant PPA, the most common NPS in behavioural variant FTD and semantic variant PPA were loss of sympathy/empathy and poor response to social/emotional cues (part of FTD Module). Patients with primary psychiatric disorders and behavioural variant FTD showed the most severe behavioural problems on both the NPI as well as the NPI with FTD Module. The NPI with FTD Module correctly classified more FTD patients than the NPI alone. By quantifying common NPS in FTD the NPI with FTD Module has large diagnostic potential. Future studies should investigate whether it can also prove a useful addition to the NPI in therapeutic trials.

Indexed as

Alzheimer DiseaseFrontotemporal DementiaBehavioral SymptomsCaregiversHumansClassificationDementiaFTDNeuropsychiatric inventoryNeuropsychiatric symptoms

Identifiers

PMID36811680
PMCPMC10129920
OpenAlexW4321480529

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.