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Article type: Research Article
Authors: Consonni, Monica; | Iannaccone, Sandro | Cerami, Chiara | Frasson, Paola | Lacerenza, Marco | Lunetta, Christian | Corbo, Massimo | Cappa, Stefano F.;
Affiliations: Department of Clinical Neurosciences and Division of Neuroscience, San Raffaele Scientific Institute, Milan, Italy | Vita-Salute University, Via Olgettina, Milan, Italy | NEuroMuscular Omnicentre – Fondazione Serena Onlus, Niguarda Ca' Granda Hospital, Milan, Italy
Note: [] Corresponding author: Monica Consonni, PhD, Department of Clinical Neurosciences, San Raffaele Turro Hospital, Via Stamira d'Ancona 20, Milan 20127, Italy. Tel.: +39 02 2643 3305; Fax: +39 02 2643 3394 (5798); E-mail: [email protected]
Abstract: OBJECTIVE: The study aims to assess the spectrum of cognitive and behavioural disorders in patients affected by Amyotrophic Lateral Sclerosis (ALS) according to the recent consensus criteria [9]. The study also intends to assess the impact of physical disability on cognitive and behavioural abnormalities. METHODS: Detailed neurological, neuropsychological and neurobehavioral evaluations were administered to 23 ALS patients, 11 Lower Motor Neuron Disease (LMND) patients and 39 healthy controls. Strong et al.'s criteria [9] were applied to diagnose the presence of cognitive/behavioural impairment. Clinical and neuropsychological scores were used for group comparisons and correlation analyses. RESULTS: In comparison with LMND and controls, a subgroup of ALS patients (∼30%) manifested executive dysfunction, which was severe enough to classify them as cognitively impaired. Action naming difficulties and short-term memory deficits were also observed. Aspontaneity, disorganization and mental rigidity reached clinical relevance in 20% of ALS patients. A small percentage of ALS patients (13%) also had comorbid dementia. The cognitive or behavioural status was not related to the clinical features of ALS. CONCLUSION: The use of consensus criteria for cognitive and behavioural impairment and the comparison with the LMND group proved useful in defining the spectrum of non-motor manifestations of ALS.
Keywords: Amyotrophic Lateral Sclerosis, Lower Motor Neuron Disease, cognitive impairment, behavioural impairment, dysexecutive syndrome, motor disability
DOI: 10.3233/BEN-2012-110202
Journal: Behavioural Neurology, vol. 27, no. 2, pp. 143-153, 2013
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