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散发性和家族性阿尔茨海默病中颜色-颜色短期记忆结合的特定缺陷。

Specific deficit of colour-colour short-term memory binding in sporadic and familial Alzheimer's disease.

机构信息

Human Cognitive Neuroscience and Centre for Cognitive Ageing and Cognitive Epidemiology, Psychology, University of Edinburgh, Edinburgh, UK.

出版信息

Neuropsychologia. 2011 Jun;49(7):1943-52. doi: 10.1016/j.neuropsychologia.2011.03.022. Epub 2011 Mar 22.

Abstract

Short-term memory binding of visual features which are processed across different dimensions (shape-colour) is impaired in sporadic Alzheimer's disease, familial Alzheimer's disease, and in asymptomatic carriers of familial Alzheimer's disease. This study investigated whether Alzheimer's disease also impacts on within-dimension binding processes. The study specifically explored whether visual short-term memory binding of features of the same type (colour-colour) is sensitive to Alzheimer's disease. We used a neuropsychological battery and a short-term memory binding task to assess patients with sporadic Alzheimer's disease (Experiment 1), familial Alzheimer's disease (Experiment 2) due to the mutation E280A of the Presenilin-1 gene and asymptomatic carriers of the mutation. The binding task assessed change detection within arrays of unicoloured objects (Colour Only) or bicoloured objects the colours of which had to be remembered separately (Unbound Colours) or together (Bound Colours). Performance on the Bound Colours condition (1) explained the largest proportion of variance between patients (sporadic and familial Alzheimer's disease), (2) combined more sensitivity and specificity for the disease than other more traditional neuropsychological tasks, (3) identified asymptomatic carriers of the mutation even when traditional neuropsychological measures and other measures of short-term memory did not and, (4) contrary to shape-colour binding, correlated with measures of hippocampal functions. Colour-colour binding and shape-colour binding both appear to be sensitive to AD even though they seem to rely on different brain mechanisms.

摘要

跨不同维度(形状-颜色)处理的视觉特征的短期记忆绑定在散发性阿尔茨海默病、家族性阿尔茨海默病和家族性阿尔茨海默病无症状携带者中受损。本研究调查了阿尔茨海默病是否也会影响维度内绑定过程。该研究特别探讨了相同类型的特征(颜色-颜色)的视觉短期记忆绑定是否对阿尔茨海默病敏感。我们使用神经心理学测试和短期记忆绑定任务来评估散发性阿尔茨海默病患者(实验 1)、家族性阿尔茨海默病患者(实验 2),这些患者是由于早老素-1 基因的 E280A 突变和无症状的突变携带者。绑定任务评估了在单一颜色物体的数组(仅颜色)或颜色必须分别(未绑定颜色)或一起(绑定颜色)记住的双色物体的数组内的变化检测。在绑定颜色条件下的表现(1)解释了患者(散发性和家族性阿尔茨海默病)之间最大比例的方差,(2)与其他更传统的神经心理学任务相比,结合了更高的敏感性和特异性用于该疾病,(3)即使传统的神经心理学测量和其他短期记忆测量都没有,也能识别出突变的无症状携带者,(4)与形状-颜色绑定相反,与海马功能的测量相关。即使它们似乎依赖于不同的大脑机制,颜色-颜色绑定和形状-颜色绑定似乎都对 AD 敏感。

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