Published in

Wiley, European Journal of Neurology, 3(30), p. 606-611, 2022

DOI: 10.1111/ene.15652

Links

Tools

Export citation

Search in Google Scholar

Prevalence and determinants of language impairment in non‐demented amyotrophic lateral sclerosis patients

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

Full text: Unavailable

Green circle
Preprint: archiving allowed
Orange circle
Postprint: archiving restricted
Red circle
Published version: archiving forbidden
Data provided by SHERPA/RoMEO

Abstract

AbstractBackground and purposeThis study aimed at estimating the prevalence of language impairment (LI) in a large, clinic‐based cohort of non‐demented amyotrophic lateral sclerosis (ALS) patients and assessing its underpinnings at motor and non‐motor levels.MethodsNon‐demented ALS patients (N = 348) underwent the Edinburgh Cognitive and Behavioural ALS Screen (ECAS), as well as an assessment of behavioural/psychiatric and motor‐functional features. The prevalence of LI was estimated based on the proportion of patients showing a performance below the age‐ and education‐adjusted cut‐off on the ECAS‐Language. Multiple regression models were run to assess the determinants of language functioning and impairment.ResultsThe prevalence of LI was 22.7%. 46.6% of the variance of ECAS‐Language scores remained unexplained, with only the ECAS‐Executive positively predicting them (p < 0.001; η2 = 0.07). Similarly, only a lower score on the ECAS‐Executive predicted a higher probability of a below cut‐off ECAS‐Language performance (p < 0.001). Spelling and Naming tasks were the major drivers of ECAS‐Language performance.ConclusionsThis study suggests that, in non‐demented ALS patients, LI occurs in ≈23% of cases, is significantly driven by executive dysfunction but, at the same time, partially independent of it and is not associated with other motor or non‐motor features.