Social cognition deficits in amyotrophic lateral sclerosis: A pilot cross‐sectional population‐based study

Background and purpose Social cognition (SC) deficits are included in amyotrophic lateral sclerosis (ALS)–frontotemporal spectrum disorder revised diagnostic criteria. However, SC performance among ALS patients is heterogeneous due to the phenotypic variability of the disease and the wide range of n...

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Veröffentlicht in:European journal of neurology 2022-08, Vol.29 (8), p.2211-2219
Hauptverfasser: Palumbo, Francesca, Iazzolino, Barbara, Peotta, Laura, Canosa, Antonio, Manera, Umberto, Grassano, Maurizio, Casale, Federico, Pellegrino, Giorgio, Rizzone, Mario Giorgio, Vasta, Rosario, Moglia, Cristina, Chiò, Adriano, Calvo, Andrea
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Sprache:eng
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Zusammenfassung:Background and purpose Social cognition (SC) deficits are included in amyotrophic lateral sclerosis (ALS)–frontotemporal spectrum disorder revised diagnostic criteria. However, SC performance among ALS patients is heterogeneous due to the phenotypic variability of the disease and the wide range of neuropsychological tools employed. The aim of the present study was to assess facial emotion recognition and theory of mind in ALS patients compared to controls and to evaluate correlations with the other cognitive domains and degree of motor impairment. Methods Eighty‐three patients and 42 controls underwent a cognitive evaluation and SC assessment through the Ekman 60 Faces Test (EK‐60F), the Reading the Mind in the Eyes Test–36 Faces (RMET‐36), and the Story‐Based Empathy Task (SET). Results ALS patients showed significantly worse performance compared to controls in EK‐60F global score (p 
ISSN:1351-5101
1468-1331
DOI:10.1111/ene.15388