Trajectories of behavior and social cognition in behavioral variant frontotemporal dementia and primary psychiatric disorders: A call for better operationalization of socioemotional changes

Author:

Fieldhouse Jay L. P.12ORCID,van Engelen Marie‐Paule E.12ORCID,Handgraaf Dédé12,de Boer Sterre C. M.12,van ’t Hooft Jochum J.12ORCID,Schouws Sigfried N. T. M.34,van Grootheest Daniël345,Kerssens Cora345,Duits Flora H.12,van Harten Argonde C.12,Oudega Mardien L.12345,Vijverberg Everard G. B.12,Pijnenburg Yolande A. L.12

Affiliation:

1. Department of Neurology, Alzheimer Center Amsterdam Amsterdam University Medical Center, location Vrije Universiteit Medical Center Amsterdam the Netherlands

2. Amsterdam Neuroscience, Neurodegeneration Amsterdam the Netherlands

3. Department of Psychiatry Amsterdam University Medical Center, location Vrije Universiteit Medical Center Amsterdam the Netherlands

4. GGZ inGeest Mental Health Care Amsterdam the Netherlands

5. Amsterdam Neuroscience, Mood, Anxiety, Psychosis, Sleep, and Stress Amsterdam the Netherlands

Abstract

AbstractBackground and purposeBehavioral variant frontotemporal dementia (bvFTD) and primary psychiatric disorders (PPD), such as mood, psychotic, and autism spectrum disorders, share similar clinical characteristics of behavior and social cognition. Better understanding of clinical progression in bvFTD and PPD is essential for adequate disease monitoring and trial design.MethodsIn this longitudinal study (N = 89), patients with bvFTD and PPD with at least one follow‐up assessment were included from the Social Brain Project of the Alzheimer Center Amsterdam. Behavioral change and social cognitive decline were assessed via informant‐rated questionnaires (Cambridge Behavioral Inventory–Revised, Frontal Behavioral Inventory [FBI], Stereotypy Rating Inventory, Frontotemporal Dementia Rating Scale, Revised Self‐Monitoring Scale [RSMS]‐caregiver) and patient assessment (Ekman 60‐Faces Test, RSMS‐patient, Emotional Contagion Scale). Clinical trajectories (median = 1.4 years, interquartile range = 1.0–2.2) were examined using linear mixed models. In a subsample, associations with baseline serum neurofilament light (sNfL) were examined.ResultsAt baseline, behavioral and social cognitive symptoms were similar between diagnosis groups, except for poorer emotion recognition in bvFTD. Over time, behavioral symptoms worsened in bvFTD, whereas most measures remained stable and the FBI improved in PPD. Regarding social cognition, emotion recognition and caregiver‐reported socioemotional sensitivity worsened in bvFTD and remained stable in PPD. Patient‐reported social cognitive measures did not change over time. Higher sNfL was associated with faster behavioral change.ConclusionsTrajectories of behavior and social cognition differentiate bvFTD from PPD, provided that social cognition is not patient‐reported. Therefore, we stress the need to optimize longitudinal social cognitive assessment in bvFTD. sNfL may be a useful prognostic marker of behavioral progression in neuropsychiatric populations.

Publisher

Wiley

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