4.4 Article

Behavioural changes predict poorer survival in amyotrophic lateral sclerosis

期刊

BRAIN AND COGNITION
卷 150, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bandc.2021.105710

关键词

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

资金

  1. Beryl-Bayley Post-doctorate Fellowship, Motor Neuron Disease Research Institute of Australia
  2. National Health and Medical Research Council of Australia Program [1132524, 1153439, 1156093]
  3. National Health and Medical Research Council of Australia [1153439] Funding Source: NHMRC

向作者/读者索取更多资源

The presence of behavioral and cognitive impairments in ALS patients is associated with poor survival outcomes. The MiND-B and ACE inventories are simple and efficient clinical tools that can aid in the prognostication of this patient population in multidisciplinary ALS clinics.
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.

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