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Addition of the FTD Module to the Neuropsychiatric Inventory improves classification of frontotemporal dementia spectrum disorders
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),...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10129920/ https://www.ncbi.nlm.nih.gov/pubmed/36811680 http://dx.doi.org/10.1007/s00415-023-11596-3 |
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author | Jiskoot, Lize C. Russell, Lucy L. Greaves, Caroline V. van Schaik, Esther van den Berg, Esther Poos, Jackie M. de Boer, Liset Donker Kaat, Laura Seelaar, Harro Pijnenburg, Yolande A. L. van Swieten, John C. Rohrer, Jonathan D. |
author_facet | Jiskoot, Lize C. Russell, Lucy L. Greaves, Caroline V. van Schaik, Esther van den Berg, Esther Poos, Jackie M. de Boer, Liset Donker Kaat, Laura Seelaar, Harro Pijnenburg, Yolande A. L. van Swieten, John C. Rohrer, Jonathan D. |
author_sort | Jiskoot, Lize C. |
collection | PubMed |
description | 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00415-023-11596-3. |
format | Online Article Text |
id | pubmed-10129920 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-101299202023-04-27 Addition of the FTD Module to the Neuropsychiatric Inventory improves classification of frontotemporal dementia spectrum disorders Jiskoot, Lize C. Russell, Lucy L. Greaves, Caroline V. van Schaik, Esther van den Berg, Esther Poos, Jackie M. de Boer, Liset Donker Kaat, Laura Seelaar, Harro Pijnenburg, Yolande A. L. van Swieten, John C. Rohrer, Jonathan D. J Neurol Original Communication 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00415-023-11596-3. Springer Berlin Heidelberg 2023-02-22 2023 /pmc/articles/PMC10129920/ /pubmed/36811680 http://dx.doi.org/10.1007/s00415-023-11596-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Communication Jiskoot, Lize C. Russell, Lucy L. Greaves, Caroline V. van Schaik, Esther van den Berg, Esther Poos, Jackie M. de Boer, Liset Donker Kaat, Laura Seelaar, Harro Pijnenburg, Yolande A. L. van Swieten, John C. Rohrer, Jonathan D. Addition of the FTD Module to the Neuropsychiatric Inventory improves classification of frontotemporal dementia spectrum disorders |
title | Addition of the FTD Module to the Neuropsychiatric Inventory improves classification of frontotemporal dementia spectrum disorders |
title_full | Addition of the FTD Module to the Neuropsychiatric Inventory improves classification of frontotemporal dementia spectrum disorders |
title_fullStr | Addition of the FTD Module to the Neuropsychiatric Inventory improves classification of frontotemporal dementia spectrum disorders |
title_full_unstemmed | Addition of the FTD Module to the Neuropsychiatric Inventory improves classification of frontotemporal dementia spectrum disorders |
title_short | Addition of the FTD Module to the Neuropsychiatric Inventory improves classification of frontotemporal dementia spectrum disorders |
title_sort | addition of the ftd module to the neuropsychiatric inventory improves classification of frontotemporal dementia spectrum disorders |
topic | Original Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10129920/ https://www.ncbi.nlm.nih.gov/pubmed/36811680 http://dx.doi.org/10.1007/s00415-023-11596-3 |
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