The Edinburgh Cognitive and Behavioural Amyotrophic Lateral Sclerosis Screen: A cross-sectional comparison of established screening tools in a German-Swiss population

Abstract The Edinburgh Cognitive and Behavioural ALS Screen (ECAS) has recently been developed as a fast and easy cognitive screening tool specifically designed for patients with motor impairments in routine clinical use. The German/Swiss-German version of the ECAS was validated in a German-Swiss consortium. One hundred and thirty-six non-demented ALS patients and 160 healthy controls were included in the study. In addition, the Frontal Assessment Battery (FAB), Montreal Cognitive Assessment (MoCA) and Consortium to Establish a Registry for Alzheimer's Disease plus Scale (CERAD plus) were administered to subgroups of patients. Results showed that administration of ECAS was fast (mean 24 min). Similar to the population in the UK version, ALS patients performed significantly worse in the ALS-specific functions (p < 0.001), specifically in the domain of language (p < 0.001), verbal fluency (p = 0.005) and executive functions (p = 0.02), but not for the non-ALS-specific functions. Carers reported behavioural abnormalities in about 30% and psychotic symptoms in 6% of the patients. Compared to ECAS, FAB, MoCA and CERAD were more generic and performance was not adjusted to motor speed. We conclude that the German/Swiss-German version of the ECAS is a fast and easy to administer cognitive screening instrument sensitive for ALS-specific dysfunctions and behaviour change.

[1]  Elaine Niven,et al.  Screening for cognition and behaviour changes in ALS , 2014, Amyotrophic lateral sclerosis & frontotemporal degeneration.

[2]  S. Kalra,et al.  Screening for frontal lobe and general cognitive impairment in patients with amyotrophic lateral sclerosis , 2014, Journal of the Neurological Sciences.

[3]  John L. Robinson,et al.  Sequential distribution of pTDP-43 pathology in behavioral variant frontotemporal dementia (bvFTD) , 2014, Acta Neuropathologica.

[4]  O. Hardiman,et al.  Aggregation of neurologic and neuropsychiatric disease in amyotrophic lateral sclerosis kindreds: A population‐based case–control cohort study of familial and sporadic amyotrophic lateral sclerosis , 2013, Annals of neurology.

[5]  Niels Birbaumer,et al.  Quality of life in fatal disease: the flawed judgement of the social environment , 2013, Journal of Neurology.

[6]  L. Goldstein,et al.  Changes in cognition and behaviour in amyotrophic lateral sclerosis: nature of impairment and implications for assessment , 2013, The Lancet Neurology.

[7]  L. H. van den Berg,et al.  Response to ‘Exploring limits of neuropsychological screening in ALS: The FAB problem’ , 2013, Amyotrophic lateral sclerosis & frontotemporal degeneration.

[8]  I. Appollonio,et al.  Exploring limits of neuropsychological screening in ALS: The FAB problem , 2013, Amyotrophic lateral sclerosis & frontotemporal degeneration.

[9]  L. H. van den Berg,et al.  Is the Frontal Assessment Battery reliable in ALS patients? , 2013, Amyotrophic lateral sclerosis & frontotemporal degeneration.

[10]  Kevin A Hallgren,et al.  Computing Inter-Rater Reliability for Observational Data: An Overview and Tutorial. , 2012, Tutorials in quantitative methods for psychology.

[11]  A. Chiò,et al.  Cognitive screening in patients with amyotrophic lateral sclerosis in early stages , 2012, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

[12]  David Heckerman,et al.  A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD , 2011, Neuron.

[13]  O. Hardiman,et al.  The syndrome of cognitive impairment in amyotrophic lateral sclerosis: a population-based study , 2011, Journal of Neurology, Neurosurgery & Psychiatry.

[14]  Thomas H. Bak シンポジウム19―1 認知症研究の新しい視点 Learning from History-FTD,ALS and Behaviour , 2010 .

[15]  M. York,et al.  Detecting frontotemporal dysfunction in ALS: Utility of the ALS Cognitive Behavioral Screen (ALS-CBS™) , 2010, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

[16]  R. D. de Haan,et al.  The cognitive profile of amyotrophic lateral sclerosis: A meta-analysis , 2010, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

[17]  M. Freedman,et al.  Consensus criteria for the diagnosis of frontotemporal cognitive and behavioural syndromes in amyotrophic lateral sclerosis , 2009, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

[18]  E. Beghi,et al.  Prognostic factors in ALS: A critical review , 2009, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

[19]  D. Neary,et al.  Behaviour in amyotrophic lateral sclerosis , 2008, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

[20]  L. Goldstein,et al.  A rapid screening battery to identify frontal dysfunction in patients with ALS , 2006, Neurology.

[21]  K. Marder,et al.  A screening assessment of cognitive impairment in patients with ALS , 2007, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

[22]  P. Eslinger,et al.  A rapid screening battery to identify frontal dysfunction in patients with ALS , 2006, Neurology.

[23]  Bruce L. Miller,et al.  Ubiquitinated TDP-43 in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis , 2006, Science.

[24]  S H Appel,et al.  Prevalence and patterns of cognitive impairment in sporadic ALS , 2005, Neurology.

[25]  J. Cummings,et al.  The Montreal Cognitive Assessment, MoCA: A Brief Screening Tool For Mild Cognitive Impairment , 2005, Journal of the American Geriatrics Society.

[26]  R. Mohs,et al.  Consortium to establish a registry for Alzheimer's disease (CERAD) clinical and neuropsychological assessment of Alzheimer's disease. , 2002, Psychopharmacology bulletin.

[27]  D. Royall,et al.  The FAB: A frontal assessment battery at bedside , 2001, Neurology.

[28]  J. Hodges,et al.  Motor neurone disease, dementia and aphasia: coincidence, co-occurrence or continuum? , 2001, Journal of Neurology.

[29]  I Litvan,et al.  The FAB: A frontal assessment battery at bedside , 2000, Neurology.

[30]  L. Goldstein,et al.  Verbal fluency and executive dysfunction in amyotrophic lateral sclerosis (ALS) , 2000, Neuropsychologia.

[31]  M. Swash,et al.  El Escorial revisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis , 2000, Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases.

[32]  H. Herzog,et al.  Frontal lobe function in amyotrophic lateral sclerosis: a neuropsychologic and positron emission tomography study , 1992, Acta neurologica Scandinavica.

[33]  Y. Mitsuyama Presenile dementia with motor neuron disease in Japan: clinico-pathological review of 26 cases. , 1984, Journal of neurology, neurosurgery, and psychiatry.

[34]  A. Paetau,et al.  Classic amyotrophic lateral sclerosis with dementia. , 1982, Archives of neurology.

[35]  Jacob Cohen A Coefficient of Agreement for Nominal Scales , 1960 .

[36]  L. H. Ziegler PSYCHOTIC AND EMOTIONAL PHENOMENA ASSOCIATED WITH AMYOTROPHIC LATERAL SCLEROSIS , 1930 .

[37]  T. Bak [Learning from history: FTD, ALS and behaviour]. , 2010, Rinsho shinkeigaku = Clinical neurology.