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A Cross‐sectional population‐based investigation into behavioral change in amyotrophic lateral sclerosis: subphenotypes, staging, cognitive predictors, and survival

OBJECTIVE: Amyotrophic Lateral Sclerosis (ALS) is a clinically heterogeneous neurodegenerative disorder associated with cognitive and behavioral impairment. The primary aim of this study was to identify behavioral subphenotypes in ALS using a custom designed behavioral assessment tool (Beaumont Beha...

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Autores principales: Burke, Tom, Pinto‐Grau, Marta, Lonergan, Katie, Bede, Peter, O'Sullivan, Meabhdh, Heverin, Mark, Vajda, Alice, McLaughlin, Russell L., Pender, Niall, Hardiman, Orla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5420811/
https://www.ncbi.nlm.nih.gov/pubmed/28491898
http://dx.doi.org/10.1002/acn3.407
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author Burke, Tom
Pinto‐Grau, Marta
Lonergan, Katie
Bede, Peter
O'Sullivan, Meabhdh
Heverin, Mark
Vajda, Alice
McLaughlin, Russell L.
Pender, Niall
Hardiman, Orla
author_facet Burke, Tom
Pinto‐Grau, Marta
Lonergan, Katie
Bede, Peter
O'Sullivan, Meabhdh
Heverin, Mark
Vajda, Alice
McLaughlin, Russell L.
Pender, Niall
Hardiman, Orla
author_sort Burke, Tom
collection PubMed
description OBJECTIVE: Amyotrophic Lateral Sclerosis (ALS) is a clinically heterogeneous neurodegenerative disorder associated with cognitive and behavioral impairment. The primary aim of this study was to identify behavioral subphenotypes in ALS using a custom designed behavioral assessment tool (Beaumont Behavioural Inventory, BBI). Secondary aims were to (1) investigate the predictive nature of cognitive assessment on behavioral change, (2) report the behavioral profile associated with the C9orf72 expansion, (3) categorize behavioral change through disease staging, and (4) to investigate the relationship between cross‐sectional behavioral classification and survival. METHODS: A cross‐sectional population‐based research design was applied to examine behavioral data from ALS patients (n = 317) and healthy controls (n = 66). Patients were screened for the C9orf72 repeat expansion. A subcohort of ALS patients completed an extensive cognitive assessment battery (n = 65), to investigate predictors of behavior change. Principal component analysis (PCA) determined factors associated with altered behavior. Survival data were extracted from the Irish ALS register. RESULTS: No behavioral changes were reported in 180 patients (57%); 95 patients had mild‐moderate behavioral change (30%); 42 patients met the cut‐off for Clinically Severe Behavioral Change (13%), suggestive of a bvFTD diagnosis. The most frequently endorsed behaviors in ALS were reduced concern for hygiene (36.8%), irritability (36.2%), new unusual habits (33.4%), and increased apathy (31.1%). Five independent factors were identified through factor analysis. Social cognitive performance was predictive of behavior change (P = 0.031), yielding an R (2) = 0.188. Behavioral categorization (mild/moderate/severe) at the time of assessment was not associated with survival (P = 0.198). INTERPRETATION: These data imply the presence of distinct subphenotypes of behavioral change in ALS, which most likely reflect subcategories of extramotor network disruption.
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spelling pubmed-54208112017-05-10 A Cross‐sectional population‐based investigation into behavioral change in amyotrophic lateral sclerosis: subphenotypes, staging, cognitive predictors, and survival Burke, Tom Pinto‐Grau, Marta Lonergan, Katie Bede, Peter O'Sullivan, Meabhdh Heverin, Mark Vajda, Alice McLaughlin, Russell L. Pender, Niall Hardiman, Orla Ann Clin Transl Neurol Research Articles OBJECTIVE: Amyotrophic Lateral Sclerosis (ALS) is a clinically heterogeneous neurodegenerative disorder associated with cognitive and behavioral impairment. The primary aim of this study was to identify behavioral subphenotypes in ALS using a custom designed behavioral assessment tool (Beaumont Behavioural Inventory, BBI). Secondary aims were to (1) investigate the predictive nature of cognitive assessment on behavioral change, (2) report the behavioral profile associated with the C9orf72 expansion, (3) categorize behavioral change through disease staging, and (4) to investigate the relationship between cross‐sectional behavioral classification and survival. METHODS: A cross‐sectional population‐based research design was applied to examine behavioral data from ALS patients (n = 317) and healthy controls (n = 66). Patients were screened for the C9orf72 repeat expansion. A subcohort of ALS patients completed an extensive cognitive assessment battery (n = 65), to investigate predictors of behavior change. Principal component analysis (PCA) determined factors associated with altered behavior. Survival data were extracted from the Irish ALS register. RESULTS: No behavioral changes were reported in 180 patients (57%); 95 patients had mild‐moderate behavioral change (30%); 42 patients met the cut‐off for Clinically Severe Behavioral Change (13%), suggestive of a bvFTD diagnosis. The most frequently endorsed behaviors in ALS were reduced concern for hygiene (36.8%), irritability (36.2%), new unusual habits (33.4%), and increased apathy (31.1%). Five independent factors were identified through factor analysis. Social cognitive performance was predictive of behavior change (P = 0.031), yielding an R (2) = 0.188. Behavioral categorization (mild/moderate/severe) at the time of assessment was not associated with survival (P = 0.198). INTERPRETATION: These data imply the presence of distinct subphenotypes of behavioral change in ALS, which most likely reflect subcategories of extramotor network disruption. John Wiley and Sons Inc. 2017-04-11 /pmc/articles/PMC5420811/ /pubmed/28491898 http://dx.doi.org/10.1002/acn3.407 Text en © 2017 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Burke, Tom
Pinto‐Grau, Marta
Lonergan, Katie
Bede, Peter
O'Sullivan, Meabhdh
Heverin, Mark
Vajda, Alice
McLaughlin, Russell L.
Pender, Niall
Hardiman, Orla
A Cross‐sectional population‐based investigation into behavioral change in amyotrophic lateral sclerosis: subphenotypes, staging, cognitive predictors, and survival
title A Cross‐sectional population‐based investigation into behavioral change in amyotrophic lateral sclerosis: subphenotypes, staging, cognitive predictors, and survival
title_full A Cross‐sectional population‐based investigation into behavioral change in amyotrophic lateral sclerosis: subphenotypes, staging, cognitive predictors, and survival
title_fullStr A Cross‐sectional population‐based investigation into behavioral change in amyotrophic lateral sclerosis: subphenotypes, staging, cognitive predictors, and survival
title_full_unstemmed A Cross‐sectional population‐based investigation into behavioral change in amyotrophic lateral sclerosis: subphenotypes, staging, cognitive predictors, and survival
title_short A Cross‐sectional population‐based investigation into behavioral change in amyotrophic lateral sclerosis: subphenotypes, staging, cognitive predictors, and survival
title_sort cross‐sectional population‐based investigation into behavioral change in amyotrophic lateral sclerosis: subphenotypes, staging, cognitive predictors, and survival
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5420811/
https://www.ncbi.nlm.nih.gov/pubmed/28491898
http://dx.doi.org/10.1002/acn3.407
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