Suppr超能文献

Dual memory task impairment in E280A presenilin-1 mutation carriers.

作者信息

MacPherson Sarah E, Parra Mario A, Moreno Sonia, Lopera Francisco, Della Sala Sergio

机构信息

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

Human Cognitive Neuroscience, Department of Psychology, University of Edinburgh, UK Centre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, UK Neuroscience Group, University of Antioquia, SIU (Sede de Investigaciones Universitaria), Antioquia, Medellin, Colombia Scottish Dementia Clinical Research Network, NHS Scotland, UK Alzheimer Scotland Dementia Research Centre, University of Edinburgh, UK UDP-INECO Foundation Core on Neuroscience (UIFCoN), Diego Portales University, Santiago, Chile.

出版信息

J Alzheimers Dis. 2015;44(2):481-92. doi: 10.3233/JAD-140990.

Abstract

Patients with sporadic Alzheimer's disease (AD) are impaired in their ability to perform two tasks concurrently compared to healthy younger and older adults, despite being able to successfully perform the tasks on their own reasonably well. Dual task impairments have also been found in those individuals with an E280A presenilin-1 genetic mutation but who do not yet meet the criteria for AD. The aim of the current study is to determine whether this dual task deficit is specific to the given combination of tasks performed simultaneously or whether it reflects a general deficit in the ability to coordinate two tasks. Thirty-one carriers of the gene mutation who did not meet the criteria for AD and 38 non-carriers were asked to perform two memory tasks simultaneously. The familial AD carriers showed significant dual task decrements compared to those family members without the gene mutation. The findings support the notion that a deficit in the mechanism responsible for coordinating the performance of two tasks may be a clinical marker for the early detection of AD due to the E280A presenilin-1 gene mutation.

摘要

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验