| Literature DB >> 27768047 |
Jürgen Keller1, Martin Gorges1, Helena E A Aho-Özhan1, Ingo Uttner1, Erich Schneider2, Jan Kassubek1, Elmar H Pinkhardt1, Albert C Ludolph1, Dorothée Lulé3.
Abstract
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder with pathological involvement of upper and lower motoneurons, subsequently leading to progressive loss of motor and speech abilities. In addition, cognitive functions are impaired in a subset of patients. To evaluate these potential deficits in severely physically impaired ALS patients, eye-tracking is a promising means to conduct cognitive tests. The present article focuses on how eye movements, an indirect means of communication for physically disabled patients, can be utilized to allow for detailed neuropsychological assessment. The requirements, in terms of oculomotor parameters that have to be met for sufficient eye-tracking in ALS patients are presented. The properties of stimuli, including type of neuropsychological tests and style of presentation, best suited to successfully assess cognitive functioning, are also described. Furthermore, recommendations regarding procedural requirements are provided. Overall, this methodology provides a reliable, easy to administer and fast approach for assessing cognitive deficits in patients who are unable to speak or write such as patients with severe ALS. The only confounding factor might be deficits in voluntary eye movement control in a subset of ALS patients.Entities:
Mesh:
Year: 2016 PMID: 27768047 PMCID: PMC5092192 DOI: 10.3791/54634
Source DB: PubMed Journal: J Vis Exp ISSN: 1940-087X Impact factor: 1.355