Literature DB >> 33725515

Behavioural changes predict poorer survival in amyotrophic lateral sclerosis.

Chilan Nguyen1, Jashelle Caga2, Colin J Mahoney2, Matthew C Kiernan2, William Huynh3.   

Abstract

OBJECTIVE: The Motor Neuron Disease Behavioural Scale (MiND-B) is a clinically validated tool that was developed to detect behavioural dysfunction in patients with amyotrophic lateral sclerosis (ALS). The current study aimed to evaluate behavioural impairment using MiND-B, as well as cognitive dysfunction in ALS patients, and to determine their prognostic implications.
METHOD: Patients with a clinical diagnosis of ALS were prospectively recruited from a specialised multidisciplinary ALS clinic. Patients underwent behavioural assessment with the Motor Neuron Disease Behavioural Scale (MiND-B) and cognitive evaluation using the Addenbrooke's Cognitive Examination (ACE). Primary outcome measure was selected as survival time, defined by time from assessment to time of death or censor date. Univariate assessment of survival effect was carried out using Kaplan-Meier survival analysis followed by cox regression analysis to assess the effect of MiND-B and ACE scores on survival time.
RESULTS: A total of 134 patients were included in the study. MiND-B testing determined that 59% were classified as having behavioural dysfunction, with deficits associated with a significantly shorter survival time (HR 2.53, p = 0.003, 95% CI 1.3-4.6). Furthermore, regression analysis demonstrated that for every 1-point reduction in the MiND-B score, risk of death increased by 3%. ACE testing established that 33% of the cohort had evidence of cognitive dysfunction. Patients with cognitive dysfunction on ACE testing had a significantly shorter survival time than patients without cognitive impairment (HR 2.0, p = 0.042, 95% CI 1.04-3.3).
CONCLUSION: The presence of behavioural and cognitive impairments in ALS patients was associated with poor survival. The MiND-B and ACE inventories are simple and efficient clinical tools that can be administered in the multidisciplinary ALS clinic, that aid in the prognostication of this patient population.
Copyright © 2021 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Amyotrophic lateral sclerosis; Behaviour; Cognition; Motor neuron disease; Prognosis; Survival

Year:  2021        PMID: 33725515     DOI: 10.1016/j.bandc.2021.105710

Source DB:  PubMed          Journal:  Brain Cogn        ISSN: 0278-2626            Impact factor:   2.310


  5 in total

1.  A cross-sectional evaluation of acceptability of an online palliative rehabilitation program for family caregivers of people with amyotrophic lateral sclerosis and cognitive and behavioral impairments.

Authors:  Lene Klem Olesen; Karen la Cour; Heidi With; Annette Faber Mahoney; Charlotte Handberg
Journal:  BMC Health Serv Res       Date:  2022-05-24       Impact factor: 2.908

Review 2.  Pathophysiology and Treatment of Non-motor Dysfunction in Amyotrophic Lateral Sclerosis.

Authors:  Colin J Mahoney; Rebekah M Ahmed; William Huynh; Sicong Tu; Jonathan D Rohrer; Richard S Bedlack; Orla Hardiman; Matthew C Kiernan
Journal:  CNS Drugs       Date:  2021-05-15       Impact factor: 5.749

3.  Reflections of family caregivers and health professionals on the everyday challenges of caring for persons with amyotrophic lateral sclerosis and cognitive impairments: a qualitative study.

Authors:  Lene Klem Olesen; Karen la Cour; Heidi With; Charlotte Handberg
Journal:  Palliat Care Soc Pract       Date:  2022-02-15

4.  TMEM106B Acts as a Modifier of Cognitive and Motor Functions in Amyotrophic Lateral Sclerosis.

Authors:  Arianna Manini; Antonia Ratti; Alberto Brusati; Alessio Maranzano; Isabella Fogh; Silvia Peverelli; Stefano Messina; Davide Gentilini; Federico Verde; Barbara Poletti; Claudia Morelli; Vincenzo Silani; Nicola Ticozzi
Journal:  Int J Mol Sci       Date:  2022-08-17       Impact factor: 6.208

Review 5.  Emerging technologies for management of patients with amyotrophic lateral sclerosis: from telehealth to assistive robotics and neural interfaces.

Authors:  Raffaele Pugliese; Riccardo Sala; Stefano Regondi; Benedetta Beltrami; Christian Lunetta
Journal:  J Neurol       Date:  2022-01-21       Impact factor: 6.682

  5 in total

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