Kim Nam-Gyoon, Effken Judith A, Lee Ho-Won
Department of Psychology, Keimyung University, Daegu 42601, Korea.
College of Nursing, University of Arizona, Tucson, AZ 85724, USA.
Healthcare (Basel). 2022 May 2;10(5):839. doi: 10.3390/healthcare10050839.
The present study investigated whether defective affordance perception capacity underpins tool use deficits in patients with Alzheimer's disease (AD). An affordance, a concept James Gibson introduced, scales environmental objects to an animal's action capabilities, thus offering opportunities for action. Each man-made artifact carries both a primary affordance (its designed function) and secondary affordances. In Experiment 1, participants identified secondary affordances of objects as a measure of their ability to identify alternative uses of familiar tools. A single response Go/No-Go task was administered to 4 groups: AD, mild cognitive impairment (MCI), Parkinson's disease (PD), and elderly controls (EC). Groups were matched for age and years of education. The AD group performed poorest, followed by MCI, and PD and EC. EC and PD groups' results failed to reach statistical significance, and the AD group performed at chance. In Experiment 2, participants judged the physical properties of the same objects used in Experiment 1. Even AD patients performed reliably, ruling out a visual processing deficit as the basis for their poor performance in Experiment 1. Results suggest that degraded affordance detection capacity can differentiate AD from normal aging and other neurodegenerative disorders and could be an affordable marker for AD, even in the early stages of AD.
本研究调查了阿尔茨海默病(AD)患者工具使用缺陷是否由有缺陷的可供性感知能力所致。可供性是詹姆斯·吉布森提出的一个概念,它将环境物体与动物的行动能力相匹配,从而提供行动机会。每一件人造物品都具有主要可供性(其设计功能)和次要可供性。在实验1中,参与者识别物体的次要可供性,以此作为衡量他们识别熟悉工具其他用途能力的指标。对四组人员进行了单一反应的Go/No-Go任务测试:AD组、轻度认知障碍(MCI)组、帕金森病(PD)组和老年对照组(EC)。各组在年龄和受教育年限方面进行了匹配。AD组表现最差,其次是MCI组,然后是PD组和EC组。EC组和PD组的结果未达到统计学显著差异,AD组的表现处于随机水平。在实验2中,参与者判断实验1中使用的相同物体的物理属性。即使是AD患者也能可靠地完成任务,排除了视觉加工缺陷是他们在实验1中表现不佳的原因。结果表明,可供性检测能力下降可以将AD与正常衰老及其他神经退行性疾病区分开来,并且即使在AD的早期阶段,可供性检测能力下降也可能是AD的一个可行标志物。