| Literature DB >> 28054827 |
Michael J Strong1, Sharon Abrahams2, Laura H Goldstein3, Susan Woolley4, Paula Mclaughlin5, Julie Snowden6, Eneida Mioshi7, Angie Roberts-South8, Michael Benatar9, Tibor HortobáGyi10, Jeffrey Rosenfeld11, Vincenzo Silani12, Paul G Ince13, Martin R Turner14.
Abstract
This article presents the revised consensus criteria for the diagnosis of frontotemporal dysfunction in amyotrophic lateral sclerosis (ALS) based on an international research workshop on frontotemporal dementia (FTD) and ALS held in London, Canada in June 2015. Since the publication of the Strong criteria, there have been considerable advances in the understanding of the neuropsychological profile of patients with ALS. Not only is the breadth and depth of neuropsychological findings broader than previously recognised - - including deficits in social cognition and language - but mixed deficits may also occur. Evidence now shows that the neuropsychological deficits in ALS are extremely heterogeneous, affecting over 50% of persons with ALS. When present, these deficits significantly and adversely impact patient survival. It is the recognition of this clinical heterogeneity in association with neuroimaging, genetic and neuropathological advances that has led to the current re-conceptualisation that neuropsychological deficits in ALS fall along a spectrum. These revised consensus criteria expand upon those of 2009 and embrace the concept of the frontotemporal spectrum disorder of ALS (ALS-FTSD).Entities:
Keywords: Amyotrophic lateral sclerosis; behaviour; cognition; frontotemporal dementia; genetics; neuropsychology
Mesh:
Year: 2017 PMID: 28054827 PMCID: PMC7409990 DOI: 10.1080/21678421.2016.1267768
Source DB: PubMed Journal: Amyotroph Lateral Scler Frontotemporal Degener ISSN: 2167-8421 Impact factor: 4.092