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Updated: Apr 4, 2026

Eye-Tracking Control to Assess Cognitive Functions in Patients with Amyotrophic Lateral Sclerosis
Published on: October 13, 2016
Syntactic processing as a marker for cognitive impairment in amyotrophic lateral sclerosis
Stella Tsermentseli1, P Nigel Leigh2, Lorna J Taylor3
1a Faculty of Education and Health, Department of Psychology , Social Work and Counselling, University of Greenwich , London , UK.
Amyotrophic lateral sclerosis (ALS) patients show significant language impairments, particularly in syntactic processing. These deficits in comprehension and speech production are detectable with simple language tests.
Area of Science:
- Neurology
- Linguistics
- Cognitive Science
Background:
- Growing interest in cognitive changes in amyotrophic lateral sclerosis (ALS).
- Limited research on language processing (word, sentence, discourse) in ALS patients.
- Need to understand the extent and nature of language deficits in ALS.
Purpose of the Study:
- To investigate language function at word, sentence, and discourse levels in ALS patients.
- To compare language performance between ALS patients and healthy controls.
- To identify specific language deficits and their potential diagnostic value in ALS.
Main Methods:
- Recruited 26 sporadic ALS patients and 26 matched healthy controls.
- Administered standardized language tasks: confrontation naming, semantic access, syntactic comprehension.
- Utilized Quantitative Production Analysis (QPA) for connected speech (Cookie Theft picture description).
Main Results:
- ALS patients demonstrated impairments in grammatical comprehension and verb semantics.
- Discourse analysis revealed deficits in syntactic complexity and fluency in ALS patients.
- Discriminant analysis confirmed syntactic measures effectively differentiate ALS patients from controls.
Conclusions:
- Patients with ALS exhibit receptive and expressive language deficits.
- Syntactic processing appears to be the primary language impairment in ALS.
- Simple language tests can detect these syntactic deficits in ALS.
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