Neuroscience Research Australia, Barker St., PO Box 1165, Randwick, New South Wales 2031, Australia.
J Clin Neurosci. 2012 Apr;19(4):552-6. doi: 10.1016/j.jocn.2011.07.042. Epub 2012 Jan 16.
Impairment in the activities of daily living (ADL) in motor neuron disease (MND) has been little investigated. The contributions of both behavioural and motor changes on functional performance have not been explored. A postal survey in New South Wales, Australia, included assessments of ADL, behavioural change (carer-based) and MND severity. Eighty-two patients were subdivided into groups according to onset presentation: bulbar (n=23) and limb (n=59). There were significant differences in ADL performance between limb and bulbar onset groups depending on ADL task. Disability was also dependent on disease severity as measured by the Amyotrophic Lateral Sclerosis Functional Rating Scale - Revised (ALSFRS - R) score. Importantly, variance in ADL scores was dependent on both motor and behavioural factors. This study confirms the progressive disabling nature of MND, which is dependent on disease severity and shows qualitative differences depending on onset presentation. A model combining motor and behavioural changes explained 57% of variance on ADL performance, with important implications for clinical intervention.
运动神经元病(MND)患者的日常生活活动(ADL)能力受损问题鲜有研究。行为和运动变化对功能表现的影响也尚未得到探索。澳大利亚新南威尔士州进行了一项邮政调查,其中包括对 ADL、行为改变(基于照顾者的)和 MND 严重程度的评估。82 名患者根据发病表现分为两组:延髓组(n=23)和肢体组(n=59)。根据 ADL 任务,肢体和延髓发病组的 ADL 表现存在显著差异。残疾程度还取决于肌萎缩侧索硬化功能评定量表修订版(ALSFRS-R)评分所衡量的疾病严重程度。重要的是,ADL 评分的差异取决于运动和行为因素。本研究证实了 MND 的进行性致残性质,这取决于疾病严重程度,并根据发病表现显示出定性差异。一个结合运动和行为变化的模型解释了 ADL 表现 57%的方差,这对临床干预具有重要意义。