Profiling social cognition in premanifest Huntington's disease
Authors
Kate Turner, Edith Cowan UniversityFollow
Danielle Bartlett, Edith Cowan UniversityFollow
Sarah A. Grainger
Clare Eddy
Alvaro Reyes
Catarina Kordsachia
Mitchell Turner, Edith Cowan UinversityFollow
Julie C. Stout
Nellie Georgiou-Karistianis
Julie D. Henry
Mel Ziman, Edith Cowan UniversityFollow
Travis Cruickshank, Edith Cowan UniversityFollow
Document Type
Journal Article
Publication Title
Journal of the International Neuropsychological Society
Volume
28
Issue
3
First Page
pp. 217
Last Page
pp. 229
Publisher
Cambridge University Press
School
School of Medical and Health Sciences / Exercise Medicine Research Institute
RAS ID
36026
Funders
Lotterywest
Abstract
Objective: Discrepancies exist in reports of social cognition deficits in individuals with premanifest Huntington's disease (HD); however, the reason for this variability has not been investigated. The aims of this study were to (1) evaluate group- and individual-level social cognitive performance and (2) examine intra-individual variability (dispersion) across social cognitive domains in individuals with premanifest HD. Method: Theory of mind (ToM), social perception, empathy, and social connectedness were evaluated in 35 individuals with premanifest HD and 29 healthy controls. Cut-off values beneath the median and 1.5 × the interquartile range below the 25th percentile (P25 - 1.5 × IQR) of healthy controls for each variable were established for a profiling method. Dispersion between social cognitive domains was also calculated. Results: Compared to healthy controls, individuals with premanifest HD performed worse on all social cognitive domains except empathy. Application of the profiling method revealed a large proportion of people with premanifest HD fell below healthy control median values across ToM ( > 80%), social perception ( > 57%), empathy ( > 54%), and social behaviour ( > 40%), with a percentage of these individuals displaying more pronounced impairments in empathy (20%) and ToM (22%). Social cognition dispersion did not differ between groups. No significant correlations were found between social cognitive domains and mood, sleep, and neurocognitive outcomes. Conclusions: Significant group-level social cognition deficits were observed in the premanifest HD cohort. However, our profiling method showed that only a small percentage of these individuals experienced marked difficulties in social cognition, indicating the importance of individual-level assessments, particularly regarding future personalised treatments.
DOI
10.1017/S1355617721000357
Related Publications
Turner, K. E. (2021). Characterising social cognition and its predictors in individuals with premanifest Huntington’s disease.
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Comments
Turner, K., Bartlett, D., Grainger, S. A., Eddy, C., Reyes, A., Kordsachia, C., ... Cruickshank, T. (2022). Profiling social cognition in premanifest Huntington's disease. Journal of the International Neuropsychological Society, vol. 28, no. 3, pp.217-229.
https://doi.org/10.1017/S1355617721000357