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Disease trajectories in behavioural variant frontotemporal dementia, primary psychiatric and other neurodegenerative disorders presenting with behavioural change

Authors :
Mara ten Kate
Frederik Barkhof
Annemiek Dols
Betty M. Tijms
Everard G. B. Vijverberg
Charlotte E. Teunissen
Wiesje M. van der Flier
Marta Del Campo
Lianne M. Reus
Yolande A.L. Pijnenburg
Pieter Jelle Visser
Welmoed A. Krudop
Flora Gossink
RS: MHeNs - R1 - Cognitive Neuropsychiatry and Clinical Neuroscience
Psychiatrie & Neuropsychologie
Neurology
Amsterdam Neuroscience - Neurodegeneration
Radiology and nuclear medicine
NCA - Neurobiology of mental health
Clinical chemistry
Epidemiology and Data Science
APH - Mental Health
Psychiatry
Divisions
APH - Personalized Medicine
APH - Methodology
Source :
Reus, L M, Vijverberg, E G, Tijms, B M, Kate, M T, Gossink, F, Krudop, W A, Campo, M D, Teunissen, C E, Barkhof, F, van der Flier, W M, Visser, P J, Dols, A & Pijnenburg, Y A 2018, ' Disease trajectories in behavioural variant frontotemporal dementia, primary psychiatric and other neurodegenerative disorders presenting with behavioural change ', Journal of Psychiatric Research, vol. 104, pp. 183-191 . https://doi.org/10.1016/j.jpsychires.2018.07.014, Journal of Psychiatric Research, 104, 183-191. Elsevier Science, Journal of Psychiatric Research, 104, 183-191. Elsevier Limited
Publication Year :
2018

Abstract

Behavioural variant frontotemporal dementia (bvFTD) is characterized by behavioural and social cognitive disturbances, while various psychiatric and neurodegenerative disorders may have similar clinical symptoms. Since neurodegenerative disorders are eventually progressive, whereas primary psychiatric disorders are not, this study aimed to investigate whether the change in clinical symptoms over time differed between groups and which biomarkers predicted rate of decline. Disease trajectories (median follow-up = 3 years) of frontal and stereotyped behaviour, general and frontal cognitive functioning, and social cognition were examined in bvFTD (n = 34), other neurodegenerative (n = 28) and primary psychiatric disorders (n = 43), all presenting with late-onset frontal lobe syndrome (45-75 years), using linear mixed models. To gain more insight in underlying pathological processes driving disease progression, we studied the association of baseline cerebrospinal fluid (CSF) (neurofilament light (NfL) and YKL-40 levels, phosphotau181 to total tau ratio) and neuroimaging markers with disease trajectories. Frontal behavioural symptoms (e.g., disinhibition, apathy) worsened over time in bvFTD, whereas they improved in psychiatric disorders and remained stable in other neurodegenerative disorders. General and frontal cognitive decline was observed in bvFTD and other neurodegenerative disorders, but not in psychiatric disorders. None of the groups showed change in stereotypy and social cognition. For all diagnostic groups, higher CSF NfL levels were associated with faster frontal cognitive decline. A modest association was observed between caudate volume and stereotyped behaviour. Tracking frontal behavioural symptoms and cognition has potential to distinguish bvFTD from other disorders. CSF NfL levels seem to be associated with decline in frontal cognitive functioning.

Details

Language :
English
ISSN :
00223956
Database :
OpenAIRE
Journal :
Reus, L M, Vijverberg, E G, Tijms, B M, Kate, M T, Gossink, F, Krudop, W A, Campo, M D, Teunissen, C E, Barkhof, F, van der Flier, W M, Visser, P J, Dols, A & Pijnenburg, Y A 2018, ' Disease trajectories in behavioural variant frontotemporal dementia, primary psychiatric and other neurodegenerative disorders presenting with behavioural change ', Journal of Psychiatric Research, vol. 104, pp. 183-191 . https://doi.org/10.1016/j.jpsychires.2018.07.014, Journal of Psychiatric Research, 104, 183-191. Elsevier Science, Journal of Psychiatric Research, 104, 183-191. Elsevier Limited
Accession number :
edsair.doi.dedup.....de5daed03d344cd0d596e3cae7f58639
Full Text :
https://doi.org/10.1016/j.jpsychires.2018.07.014