24 results on '"Jiskoot, L. C."'
Search Results
2. Differential linguistic features of verbal fluency in behavioral variant frontotemporal dementia and primary progressive aphasia.
- Author
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van den Berg, E., Dijkzeul, J. C. M., Poos, J. M., Eikelboom, W. S., van Hemmen, J., Franzen, S., de Jong, F. J., Dopper, E. G. P., Vonk, J. M. J., Papma, J. M., Satoer, D., Jiskoot, L. C., and Seelaar, H.
- Subjects
EXECUTIVE function ,SEMANTIC memory ,FRONTOTEMPORAL dementia ,LANGUAGE ability ,REGRESSION analysis ,FRONTOTEMPORAL lobar degeneration - Abstract
Frontotemporal dementia (FTD) is an early-onset neurodegenerative disorder with a heterogeneous clinical presentation. Verbal fluency is regularly used as a sensitive measure of language ability, semantic memory, and executive functioning, but qualitative changes in verbal fluency in FTD are currently overlooked. This retrospective study examined qualitative, linguistic features of verbal fluency in 137 patients with behavioral variant (bv)FTD (n = 50), or primary progressive aphasia (PPA) [25 non-fluent variant (nfvPPA), 27 semantic variant (svPPA), and 34 logopenic variant (lvPPA)] and 25 control participants. Between-group differences in clustering, switching, lexical frequency (LF), age of acquisition (AoA), neighborhood density (ND), and word length (WL) were examined in the category and letter fluency with analysis of variance adjusted for age, sex, and the total number of words. Associations with other cognitive functions were explored with linear regression analysis. The results showed that the verbal fluency performance of patients with svPPA could be distinguished from controls and other patient groups by fewer and smaller clusters, more switches, higher LF, and lower AoA (all p < 0.05). Patients with lvPPA specifically produced words with higher ND than the other patient groups (p < 0.05). Patients with bvFTD produced longer words than the PPA groups (p < 0.05). Clustering, switching, LF, AoA, and ND—but not WL—were differentially predicted by measures of language, memory, and executive functioning (range standardized regression coefficient 0.25–0.41). In addition to the total number of words, qualitative linguistic features differ between subtypes of FTD. These features provide additional information on lexical processing and semantic memory that may aid the differential diagnosis of FTD. [ABSTRACT FROM AUTHOR]
- Published
- 2024
- Full Text
- View/download PDF
3. Cognitive profiles discriminate between genetic variants of behavioral frontotemporal dementia
- Author
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Poos, J. M., Jiskoot, L. C., Leijdesdorff, S. M. J., Seelaar, H., Panman, J. L., van der Ende, E. L., Mol, M. O., Meeter, L. H. H., Pijnenburg, Y. A. L., Donker Kaat, L., de Jong, F. J., van Swieten, J. C., Papma, J. M., and van den Berg, E.
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- 2020
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4. Correction to: Cognitive profiles discriminate between genetic variants of behavioral frontotemporal dementia
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Poos, J. M., Jiskoot, L. C., Leijdesdorff, S. M. J., Seelaar, H., Panman, J. L., van der Ende, E. L., Mol, M. O., Meeter, L. H. H., Pijnenburg, Y. A. L., Donker Kaat, L., de Jong, F. J., van Swieten, J. C., Papma, J. M., and van den Berg, E.
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- 2020
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- View/download PDF
5. Naming Assessment in Multicultural Europe
- Author
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Franzen, S., primary, van den Berg, E., additional, Ayhan, Y., additional, Satoer, D. D., additional, Türkoğlu, Ö., additional, Genç Akpulat, G. E., additional, Visch-Brink, E. G., additional, Scheffers, E. A., additional, Kranenburg, J., additional, Jiskoot, L. C., additional, van Hemmen, J., additional, and Papma, J. M., additional
- Published
- 2023
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6. Functional connectivity and microstructural white matter changes in phenocopy frontotemporal dementia
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Meijboom, R., Steketee, R. M. E., de Koning, I., Osse, R. J., Jiskoot, L. C., de Jong, F. J., van der Lugt, A., van Swieten, J. C., and Smits, M.
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- 2017
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7. Modelling the cascade of biomarker changes in GRN-related frontotemporal dementia
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Panman, J. L., Venkatraghavan, V., Van Der Ende, E. L., Steketee, R. M. E., Jiskoot, L. C., Poos, J. M., Dopper, E. G. P., Meeter, L. H. H., Kaat, L. D., Rombouts, S. A. R. B., Vernooij, M. W., Kievit, A. J. A., Premi, E., Cosseddu, M., Bonomi, E., Olives, J., Rohrer, J. D., Sanchez-Valle, R., Borroni, B., Bron, E. E., Van Swieten, J. C., Papma, J. M., Klein, S., Afonso, S., Almeida, M. R., Anderl-Straub, S., Andersson, C., Antonell, A., Archetti, S., Arighi, A., Balasa, M., Barandiaran, M., Bargallo, N., Bartha, R., Bender, B., Black, S., Butler, C., Bocchetta, M., Borrego-Ecija, S., Bras, J., Bruffaerts, R., Caroppo, P., Cash, D., Castelo-Branco, M., Convery, R., Cope, T., Danek, A., De Arriba, M., De Mendonca, A., Di Fede, G., Diaz, Z., Ducharme, S., Duro, D., Fenoglio, C., Ferreira, C. B., Finger, E., Flanagan, T., Fox, N., Freedman, M., Fumagalli, G., Gabilondo, A., Galimberti, D., Gasparotti, R., Gauthier, S., Gazzina, S., Gerhard, A., Giaccone, G., Gorostidi, A., Graff, C., Greaves, C., Guerreiro, R., Heller, C., Hoegen, T., Indakoetxea, B., Jelic, V., Karnath, H. -O., Keren, R., Laforce, R., Leitao, M. J., Levin, J., Llado, A., Loosli, S., Maruta, C., Masellis, M., Mead, S., Miltenberger, G., Van Minkelenm Sara Mitchell, R., Moore, K., Moreno, F., Nicholas, J., Oijerstedt, L., Otto, M., Ourselin, S., Padovani, A., Peakman, G., Pijnenburg, Y., Polito, C., Prioni, S., Prix, C., Rademakers, R., Redaelli, V., Rittman, T., Rogaeva, E., Rosa-Neto, P., Rossi, G., Rosser, M., Rowe, J., Santana, I., Santiago, B., Scarpini, E., Schonecker, S., Shafei, E. S. R., Shoesmith, C., Synofzik, M., Tabuas-Pereira, M., Tagliavini, F., Tartaglia, C., Tainta, M., Taipa, R., Tang-Wai, D., Thomas, D. L., Thonberg, H., Timberlake, C., Tiraboschi, P., Todd, E., Vandamme, P., Vandenberghe, R., Vandenbulcke, M., Veldsman, M., Verdelho, A., Villanua, J., Warren, J., Wilkeione, C., Elisabeth, W., Henrik, W., Zulaica, Z. M., Neurology, Physics and medical technology, Radiology & Nuclear Medicine, Clinical Genetics, and Medical Research Council
- Subjects
Male ,Oncology ,Disease ,Neuropsychological Tests ,GENFI consortium investigators ,Primary progressive aphasia ,Cognition ,Progranulins ,0302 clinical medicine ,Neurofilament Proteins ,BEHAVIORAL VARIANT ,HETEROGENEITY ,Gray Matter ,11 Medical and Health Sciences ,Language ,Psychiatry ,0303 health sciences ,Brain ,Middle Aged ,Magnetic Resonance Imaging ,White Matter ,17 Psychology and Cognitive Sciences ,ALZHEIMERS-DISEASE ,Psychiatry and Mental health ,Phenotype ,medicine.anatomical_structure ,Frontotemporal Dementia ,Disease Progression ,Biomarker (medicine) ,Female ,Life Sciences & Biomedicine ,Frontotemporal dementia ,medicine.medical_specialty ,Clinical Neurology ,EVENT-BASED MODEL ,Grey matter ,Lateralization of brain function ,White matter ,03 medical and health sciences ,SDG 3 - Good Health and Well-being ,Internal medicine ,NEUROFILAMENT LIGHT-CHAIN ,medicine ,Humans ,LOBAR DEGENERATION ,PROGRANULIN ,Aged ,030304 developmental biology ,Science & Technology ,Neurology & Neurosurgery ,business.industry ,DISEASE PROGRESSION ,medicine.disease ,Mutation ,WHITE-MATTER INTEGRITY ,Surgery ,Neurosciences & Neurology ,Neurology (clinical) ,business ,GENFI ,Biomarkers ,030217 neurology & neurosurgery ,Progressive disease - Abstract
ObjectiveProgranulin-related frontotemporal dementia (FTD-GRN) is a fast progressive disease. Modelling the cascade of multimodal biomarker changes aids in understanding the aetiology of this disease and enables monitoring of individual mutation carriers. In this cross-sectional study, we estimated the temporal cascade of biomarker changes for FTD-GRN, in a data-driven way.MethodsWe included 56 presymptomatic and 35 symptomatic GRN mutation carriers, and 35 healthy non-carriers. Selected biomarkers were neurofilament light chain (NfL), grey matter volume, white matter microstructure and cognitive domains. We used discriminative event-based modelling to infer the cascade of biomarker changes in FTD-GRN and estimated individual disease severity through cross-validation. We derived the biomarker cascades in non-fluent variant primary progressive aphasia (nfvPPA) and behavioural variant FTD (bvFTD) to understand the differences between these phenotypes.ResultsLanguage functioning and NfL were the earliest abnormal biomarkers in FTD-GRN. White matter tracts were affected before grey matter volume, and the left hemisphere degenerated before the right. Based on individual disease severities, presymptomatic carriers could be delineated from symptomatic carriers with a sensitivity of 100% and specificity of 96.1%. The estimated disease severity strongly correlated with functional severity in nfvPPA, but not in bvFTD. In addition, the biomarker cascade in bvFTD showed more uncertainty than nfvPPA.ConclusionDegeneration of axons and language deficits are indicated to be the earliest biomarkers in FTD-GRN, with bvFTD being more heterogeneous in disease progression than nfvPPA. Our data-driven model could help identify presymptomatic GRN mutation carriers at risk of conversion to the clinical stage.
- Published
- 2021
8. Data-driven staging of genetic frontotemporal dementia using multi-modal MRI
- Author
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McCarthy, J., Borroni, B., Sanchez-Valle, R., Moreno, F., Laforce, R., Graff, C., Synofzik, M., Galimberti, D., Rowe, J. B., Masellis, M., Tartaglia, M. C., Finger, E., Vandenberghe, R., de Mendonça, A., Tagliavini, F., Santana, I., Butler, C., Gerhard, A., Danek, A., Levin, J., Otto, M., Frisoni, G., Ghidoni, R., Sorbi, S., Jiskoot, L. C., Seelaar, H., van Swieten, J. C., Rohrer, J. D., Iturria-Medina, Y., Ducharme, S., Anderl-Straub, S., Andersson, C., Antonell, A., McCarthy, J., Borroni, B., Sanchez-Valle, R., Moreno, F., Laforce, R., Graff, C., Synofzik, M., Galimberti, D., Rowe, J. B., Masellis, M., Tartaglia, M. C., Finger, E., Vandenberghe, R., de Mendonça, A., Tagliavini, F., Santana, I., Butler, C., Gerhard, A., Danek, A., Levin, J., Otto, M., Frisoni, G., Ghidoni, R., Sorbi, S., Jiskoot, L. C., Seelaar, H., van Swieten, J. C., Rohrer, J. D., Iturria-Medina, Y., Ducharme, S., Anderl-Straub, S., Andersson, C., and Antonell, A.
- Abstract
Frontotemporal dementia in genetic forms is highly heterogeneous and begins many years to prior symptom onset, complicating disease understanding and treatment development. Unifying methods to stage the disease during both the presymptomatic and symptomatic phases are needed for the development of clinical trials outcomes. Here we used the contrastive trajectory inference (cTI), an unsupervised machine learning algorithm that analyzes temporal patterns in high-dimensional large-scale population datasets to obtain individual scores of disease stage. We used cross-sectional MRI data (gray matter density, T1/T2 ratio as a proxy for myelin content, resting-state functional amplitude, gray matter fractional anisotropy, and mean diffusivity) from 383 gene carriers (269 presymptomatic and 115 symptomatic) and a control group of 253 noncarriers in the Genetic Frontotemporal Dementia Initiative. We compared the cTI-obtained disease scores to the estimated years to onset (age—mean age of onset in relatives), clinical, and neuropsychological test scores. The cTI based disease scores were correlated with all clinical and neuropsychological tests (measuring behavioral symptoms, attention, memory, language, and executive functions), with the highest contribution coming from mean diffusivity. Mean cTI scores were higher in the presymptomatic carriers than controls, indicating that the method may capture subtle pre-dementia cerebral changes, although this change was not replicated in a subset of subjects with complete data. This study provides a proof of concept that cTI can identify data-driven disease stages in a heterogeneous sample combining different mutations and disease stages of genetic FTD using only MRI metrics. © 2022 The Authors. Human Brain Mapping published by Wiley Periodicals LLC.
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- 2022
9. Differential linguistic features of verbal fluency in behavioral variant frontotemporal dementia and primary progressive aphasia
- Author
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van den Berg, E., Dijkzeul, J. C. M., Poos, J. M., Eikelboom, W. S., van Hemmen, J., Franzen, S., de Jong, F. J., Dopper, E. G. P., Vonk, J. M. J., Papma, J. M., Satoer, D., Jiskoot, L. C., Seelaar, H., van den Berg, E., Dijkzeul, J. C. M., Poos, J. M., Eikelboom, W. S., van Hemmen, J., Franzen, S., de Jong, F. J., Dopper, E. G. P., Vonk, J. M. J., Papma, J. M., Satoer, D., Jiskoot, L. C., and Seelaar, H.
- Abstract
Frontotemporal dementia (FTD) is an early-onset neurodegenerative disorder with a heterogeneous clinical presentation. Verbal fluency is regularly used as a sensitive measure of language ability, semantic memory, and executive functioning, but qualitative changes in verbal fluency in FTD are currently overlooked. This retrospective study examined qualitative, linguistic features of verbal fluency in 137 patients with behavioral variant (bv)FTD (n = 50), or primary progressive aphasia (PPA) [25 non-fluent variant (nfvPPA), 27 semantic variant (svPPA), and 34 logopenic variant (lvPPA)] and 25 control participants. Between-group differences in clustering, switching, lexical frequency (LF), age of acquisition (AoA), neighborhood density (ND), and word length (WL) were examined in the category and letter fluency with analysis of variance adjusted for age, sex, and the total number of words. Associations with other cognitive functions were explored with linear regression analysis. The results showed that the verbal fluency performance of patients with svPPA could be distinguished from controls and other patient groups by fewer and smaller clusters, more switches, higher LF, and lower AoA (all p < 0.05). Patients with lvPPA specifically produced words with higher ND than the other patient groups (p < 0.05). Patients with bvFTD produced longer words than the PPA groups (p < 0.05). Clustering, switching, LF, AoA, and ND-but not WL-were differentially predicted by measures of language, memory, and executive functioning (range standardized regression coefficient 0.25-0.41). In addition to the total number of words, qualitative linguistic features differ between subtypes of FTD. These features provide additional information on lexical processing and semantic memory that may aid the differential diagnosis of FTD.
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- 2022
10. Impaired Knowledge of Social Norms in Dementia and Psychiatric Disorders:Validation of the Social Norms Questionnaire–Dutch Version (SNQ-NL)
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van den Berg, E., Poos, J. M., Jiskoot, L. C., Montagne, B., Kessels, R. P.C., Franzen, S., van Hemmen, J., Eikelboom, W. S., Heijboer, E. G.C., de Kriek, J., van der Vlist, A., de Jong, F. J., van Swieten, J. C., Seelaar, H., Papma, J. M., van den Berg, E., Poos, J. M., Jiskoot, L. C., Montagne, B., Kessels, R. P.C., Franzen, S., van Hemmen, J., Eikelboom, W. S., Heijboer, E. G.C., de Kriek, J., van der Vlist, A., de Jong, F. J., van Swieten, J. C., Seelaar, H., and Papma, J. M.
- Abstract
The Social Norms Questionnaire–Dutch version (SNQ-NL) measures the ability to understand and identify social boundaries. We examined the psychometric characteristics of the SNQ-NL and its ability to differentiate between patients with behavioral variant frontotemporal dementia (bvFTD; n = 23), Alzheimer’s dementia (AD; n = 26), chronic psychiatric disorders (n = 27), and control participants (n = 92). Between-group differences in the Total score, Break errors, and Overadhere errors were examined and associations with demographic variables and other cognitive functions were explored. Results showed that the SNQ-NL Total Score and Break errors differed between patients with AD and bvFTD, but not between patients with bvFTD and psychiatric disorders. Modest correlations with age, sex, and education were observed. The SNQ-NL Total score and Break errors correlated significantly with emotion recognition and verbal fluency but not with processing speed or mental flexibility. In conclusion, the SNQ-NL has sufficient construct validity and can be used to investigate knowledge of social norms in clinical populations.
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- 2022
11. Differential linguistic features of verbal fluency in behavioral variant frontotemporal dementia and primary progressive aphasia
- Author
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van den Berg, E., primary, Dijkzeul, J. C. M., additional, Poos, J. M., additional, Eikelboom, W. S., additional, van Hemmen, J., additional, Franzen, S., additional, de Jong, F. J., additional, Dopper, E. G. P., additional, Vonk, J. M. J., additional, Papma, J. M., additional, Satoer, D., additional, Jiskoot, L. C., additional, and Seelaar, H., additional
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- 2022
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12. Social Norms Questionnaire--Dutch Version
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van den Berg, E., primary, Poos, J. M., additional, Jiskoot, L. C., additional, Montagne, B., additional, Kessels, R. P. C., additional, Franzen, S., additional, van Hemmen, J., additional, Eikelboom, W. S., additional, Heijboer, E. G. C., additional, de Kriek, J., additional, van der Vlist, A., additional, de Jong, F. J., additional, van Swieten, J. C., additional, Seelaar, H., additional, and Papma, J. M., additional
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- 2022
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13. Impaired Knowledge of Social Norms in Dementia and Psychiatric Disorders: Validation of the Social Norms Questionnaire–Dutch Version (SNQ-NL).
- Author
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van den Berg, E., Poos, J. M., Jiskoot, L. C., Montagne, B., Kessels, R. P. C., Franzen, S., van Hemmen, J., Eikelboom, W. S., Heijboer, E. G. C., de Kriek, J., van der Vlist, A., de Jong, F. J., van Swieten, J. C., Seelaar, H., and Papma, J. M.
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STATISTICS ,ALZHEIMER'S disease ,SOCIAL perception ,RESEARCH evaluation ,ANALYSIS of variance ,SOCIAL norms ,RESEARCH methodology evaluation ,AGE distribution ,RESEARCH methodology ,CASE-control method ,COGNITION ,PSYCHOMETRICS ,HEALTH literacy ,SEX distribution ,MULTITRAIT multimethod techniques ,PEARSON correlation (Statistics) ,QUESTIONNAIRES ,DEMENTIA ,DESCRIPTIVE statistics ,DATA analysis ,DATA analysis software ,MENTAL illness ,FRONTOTEMPORAL dementia ,EDUCATIONAL attainment - Abstract
The Social Norms Questionnaire–Dutch version (SNQ-NL) measures the ability to understand and identify social boundaries. We examined the psychometric characteristics of the SNQ-NL and its ability to differentiate between patients with behavioral variant frontotemporal dementia (bvFTD; n = 23), Alzheimer's dementia (AD; n = 26), chronic psychiatric disorders (n = 27), and control participants (n = 92). Between-group differences in the Total score, Break errors, and Overadhere errors were examined and associations with demographic variables and other cognitive functions were explored. Results showed that the SNQ-NL Total Score and Break errors differed between patients with AD and bvFTD, but not between patients with bvFTD and psychiatric disorders. Modest correlations with age, sex, and education were observed. The SNQ-NL Total score and Break errors correlated significantly with emotion recognition and verbal fluency but not with processing speed or mental flexibility. In conclusion, the SNQ-NL has sufficient construct validity and can be used to investigate knowledge of social norms in clinical populations. [ABSTRACT FROM AUTHOR]
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- 2022
- Full Text
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14. Impaired Knowledge of Social Norms in Dementia and Psychiatric Disorders: Validation of the Social Norms Questionnaire–Dutch Version (SNQ-NL)
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van den Berg, E., primary, Poos, J. M., additional, Jiskoot, L. C., additional, Montagne, B., additional, Kessels, R. P. C., additional, Franzen, S., additional, van Hemmen, J., additional, Eikelboom, W. S., additional, Heijboer, E. G. C., additional, de Kriek, J., additional, van der Vlist, A., additional, de Jong, F. J., additional, van Swieten, J. C., additional, Seelaar, H., additional, and Papma, J. M., additional
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- 2021
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15. Exploring Abstract Semantic Associations in the Frontotemporal Dementia Spectrum in a Dutch Population
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Poos, J M, primary, van den Berg, E, additional, Visch-Brink, E, additional, Eikelboom, W S, additional, Franzen, S, additional, van Hemmen, J, additional, Pijnenburg, Y A L, additional, Satoer, D, additional, Dopper, E G P, additional, van Swieten, J C, additional, Papma, J M, additional, Seelaar, H, additional, and Jiskoot, L C, additional
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- 2021
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16. Exploring Abstract Semantic Associations in the Frontotemporal Dementia Spectrum in a Dutch Population.
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Poos, J M, Berg, E van den, Visch-Brink, E, Eikelboom, W S, Franzen, S, Hemmen, J van, Pijnenburg, Y A L, Satoer, D, Dopper, E G P, Swieten, J C van, Papma, J M, Seelaar, H, and Jiskoot, L C
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FRONTOTEMPORAL dementia ,NEUROPSYCHOLOGICAL tests ,CONCRETE testing ,LANGUAGE ability testing ,DIFFERENTIAL diagnosis - Abstract
Objective To investigate the differential ability of the "Test Relaties Abstracte Concepten" (TRACE), a Dutch test for abstract semantic knowledge, in frontotemporal dementia (FTD). Methods The TRACE was administered in patients with behavioral variant FTD (bvFTD; n = 16), nonfluent variant (nfvPPA; n = 10), logopenic variant (lvPPA; n = 10), and semantic variant primary progressive aphasia (svPPA; n = 9), and controls (n = 59). We examined group differences, performed correlational analyses with other neuropsychological tests and investigated discriminative ability. We compared the TRACE with a semantic association test for concrete stimuli (SAT). Results All patient groups, except nfvPPA, performed worse on the TRACE than controls (p < .01). svPPA patients performed worse than the other patient groups (p < .05). The TRACE discriminated well between patient groups, except nfvPPA, versus controls (all p < .01) and between svPPA versus other patient groups with high sensitivity (75–100%) and specificity (86%–92%). In bvFTD and nfvPPA the TRACE correlated with language tests (ρ > 0.6), whereas in svPPA the concrete task correlated (ρ ≥ 0.75) with language tests. Patients with bvFTD, nfvPPA and lvPPA performed lower on the TRACE than the SAT (p < .05), whereas patients with svPPA were equally impaired on both tasks (p = .2). Discussion We demonstrated impaired abstract semantic knowledge in patients with bvFTD, lvPPA, and svPPA, but not nfvPPA, with svPPA patients performing worse than the other subtypes. The TRACE was a good classifier between each patient group versus controls and between svPPA versus other patient groups. This highlights the value of incorporating semantic tests with abstract stimuli into standard neuropsychological assessment for early differential diagnosis of FTD subtypes. [ABSTRACT FROM AUTHOR]
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- 2022
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17. Presymptomatic changes in gray matter volume, white matter integrity and neuropsychological assessment in C9orf72 mutation carriers
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Panman, J. L., Jiskoot, L. C., Dopper, E. G. P., Serge A. Rombouts, Den Heijer, T., Franzen, S., Pijnenburg, Y. A. L., Minkelen, R., Papma, J. M., and Swieten, J. C.
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- 2016
18. Functional connectivity and microstructural white matter changes in phenocopy frontotemporal dementia
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Meijboom, R., primary, Steketee, R. M. E., additional, de Koning, I., additional, Osse, R. J., additional, Jiskoot, L. C., additional, de Jong, F. J., additional, van der Lugt, A., additional, van Swieten, J. C., additional, and Smits, M., additional
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- 2016
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19. Structural and functional brain connectivity in presymptomatic familial frontotemporal dementia
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Dopper, E. G. P., primary, Rombouts, S. A. R. B., additional, Jiskoot, L. C., additional, den Heijer, T., additional, de Graaf, J. R. A., additional, de Koning, I., additional, Hammerschlag, A. R., additional, Seelaar, H., additional, Seeley, W. W., additional, Veer, I. M., additional, van Buchem, M. A., additional, Rizzu, P., additional, and van Swieten, J. C., additional
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- 2014
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20. Structural and functional brain connectivity in presymptomatic familial frontotemporal dementia
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Dopper, E. G. P., primary, Rombouts, S. A. R. B., additional, Jiskoot, L. C., additional, Heijer, T. d., additional, Graaf, J. R. A. d., additional, Koning, I. d., additional, Hammerschlag, A. R., additional, Seelaar, H., additional, Seeley, W. W., additional, Veer, I. M., additional, van Buchem, M. A., additional, Rizzu, P., additional, and van Swieten, J. C., additional
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- 2013
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21. Increased neurofilament light chain correlates with decreased white matter integrity in presymptomatic and symptomatic granulin carriers
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Panman, J. L., Meeter, L. H. H., Dopper, E. G. P., Jiskoot, L. C., Bouts, M. J. M., Moller, C., Minkelen, R., Sanchez-Valle, R., Balasa, M., Graff, C., Oijerstedt, L., Jelic, V., Benussi, L., Ghidoni, R., Binetti, G., Barbara, B., Padovani, A., Galimberti, D., Scarpini, E., Fenoglio, C., Laforce, R. J., Vandenberghe, R., Le Ber, I., Lamari, F., Otto, M., Rohrer, J. D., Cash, D. M., Serge A. Rombouts, Teunissen, C. E., Papma, J. M., and Swieten, J. C.
22. Spontaneous speech: a robust measurement before, during and after awake brain surgery in patients with glioma.
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Collée E, Vincent AJPE, Jiskoot LC, Bos EM, Schouten JW, Dirven CMF, and Satoer D
- Abstract
Background: Patients with glioma often report language complaints with devastating effect on daily life. Analysing spontaneous speech can help to understand underlying language problems. Spontaneous speech monitoring is also of importance during awake brain surgery: it can guide tumour resection and contributes to maintaining language function. We aimed to investigate the spontaneous speech of patients with glioma in the perioperative period and the additional value of spontaneous speech analyses compared to standardised language testing., Methods: We elicited and transcribed spontaneous speech of eight patients with glioma elected for awake brain surgery preoperatively, intraoperatively and 2.0-3.5 months postoperatively. Linguistic errors were coded. Type Token Ratio, Mean Length of Utterance of words, minimal utterances, and errors were extracted from the transcriptions. Patients were categorised based on total error patterns: stable, decrease or increase during surgery. Reliable Change Index scores were calculated for all spontaneous speech variables to objectify changes between time points. Language performance on language tests was compared to spontaneous speech variables., Results: Most errors occurred in lexico-syntax, followed by phonology/articulation, syntax, and semantics. The predominant errors were Repetitions, Self-corrections, and Incomplete sentences. Most patients remained stable over time in almost all spontaneous speech variables, except in Incomplete sentences, which deteriorated in most patients postoperatively compared to intraoperatively. Some spontaneous speech variables (total errors, MLUw, TTR) gave more information on language change than a standard language test., Conclusions: While the course of spontaneous speech over time remained relatively stable in most patients, Incomplete sentences seems to be a robust marker of language difficulties patients with glioma. These errors can be prioritised in spontaneous speech analysis to save time, especially to determine intra- to postoperative deterioration. Importantly, spontaneous speech analyses can give more information on language change than standardised language testing and should therefore be used in addition to standardised language tests.
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- 2024
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23. The Naming Assessment in Multicultural Europe (NAME): Development and Validation in a Multicultural Memory Clinic.
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Franzen S, van den Berg E, Ayhan Y, Satoer DD, Türkoğlu Ö, Genç Akpulat GE, Visch-Brink EG, Scheffers EA, Kranenburg J, Jiskoot LC, van Hemmen J, and Papma JM
- Subjects
- Humans, Aged, Reproducibility of Results, Pilot Projects, Neuropsychological Tests, Europe, Neurodegenerative Diseases
- Abstract
Objective: Traditional naming tests are unsuitable to assess naming impairment in diverse populations, given the influence of culture, language, and education on naming performance. Our goal was therefore to develop and validate a new test to assess naming impairment in diverse populations: the Naming Assessment in Multicultural Europe (NAME)., Method: We carried out a multistage pilot study. First, we generated a list of 149 potentially suitable items - e.g. from published cross-linguistic word lists and other naming tests - and selected those with a homogeneous age of acquisition and word frequency across languages. We selected three to four colored photographs for each of the 73 remaining items; 194 controls selected the most suitable photographs. Thirteen items were removed after a pilot study in 15 diverse healthy controls. The final 60-item test was validated in 39 controls and 137 diverse memory clinic patients with subjective cognitive impairment, neurological/neurodegenerative disease or psychiatric disorders in the Netherlands and Turkey (mean age: 67, SD: 11). Patients were from 15 different countries; the majority completed primary education or less (53%)., Results: The NAME showed excellent reliability (Spearman-Brown coefficient: 0.95; Kuder-Richardson coefficient: 0.94) and robust correlations with other language tests ( ρ = .35-.73). Patients with AD/mixed dementia obtained lower scores on most (48/60) NAME items, with an area under the curve of 0.88. NAME scores were correlated with age and education, but not with acculturation or sex., Conclusions: The NAME is a promising tool to assess naming impairment in culturally, educationally, and linguistically diverse individuals.
- Published
- 2023
- Full Text
- View/download PDF
24. Differences in Discriminability and Response Bias on Rey Auditory Verbal Learning Test Delayed Recognition in Behavioral Variant Frontotemporal Dementia and Alzheimer's Disease.
- Author
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van den Berg E, Poos JM, Jiskoot LC, Heijnen LM, Franzen S, Steketee RME, Meijboom R, de Jong FJ, Seelaar H, van Swieten JC, and Papma JM
- Subjects
- Aged, Cognition physiology, Executive Function physiology, Female, Humans, Male, Memory, Episodic, Mental Recall physiology, Middle Aged, Neuropsychological Tests, Recognition, Psychology, Retrospective Studies, Alzheimer Disease psychology, Frontotemporal Dementia psychology, Memory Disorders diagnosis, Memory and Learning Tests
- Abstract
Objective: Episodic memory is impaired in Alzheimer's disease (AD) dementia but thought to be relatively spared in behavioral variant frontotemporal dementia (bvFTD). This view is challenged by evidence of memory impairment in bvFTD. This study investigated differences in recognition memory performance between bvFTD and AD., Method: We performed a retrospective analysis on the recognition trial of the Rey Auditory Verbal Learning Test in patients with bvFTD (n = 85), AD (n = 55), and control participants (n = 59). Age- and education-adjusted between-group analysis was performed on the total score and indices of discriminative ability and response bias. Correlations between recognition and measures of memory, language, executive functioning, and construction were examined., Results: Patients with AD had a significantly lower total recognition score than patients with bvFTD (control 28.8 ± 1.5; bvFTD 24.8 ± 4.5; AD 23.4 ± 3.6, p < .01). Both bvFTD and AD had worse discriminative ability than controls (A' control 0.96 ± 0.03; bvFTD 0.87 ± 0.03; AD 0.84 ± 0.10, p < .01), but there was no difference in response bias (B" control 0.9 ± 0.2; bvFTD 1.6 ± 1.47; AD 1.4± 1.4, p < .01). AD had worse discriminability than bvFTD (p < .05). Discriminability was associated with memory for both patient groups (median correlation coefficient r = .34) and additionally associated with language (r = .31), but not executive functioning (r = -.03) in bvFTD. Response bias was unrelated to other cognitive functions (r = -.02)., Conclusions: Discriminability, but not response bias, differentiated patients with bvFTD from AD. The presence of an impaired discrimination index suggests a "pure" (recognition) memory deficit in bvFTD.
- Published
- 2020
- Full Text
- View/download PDF
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