Department of Psychology, Human Cognitive Neuroscience and Centre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, United Kingdom.
J Int Neuropsychol Soc. 2012 Mar;18(2):234-41. doi: 10.1017/S1355617711001561. Epub 2011 Dec 2.
Previous dual task studies have demonstrated that patients with sporadic Alzheimer's disease (AD) are impaired in their ability to perform two tasks simultaneously compared with healthy controls, despite being able to successfully perform the tasks alone relatively well. Yet, it remains unclear what the earliest clinical manifestation of this dual task coordination deficit is. This study examined dual task abilities in individuals who are at risk of early-onset familial AD due to an E280A presenilin-1 mutation. Thirty-nine carriers of the gene mutation who did not meet the criteria for AD and 29 non-carrier healthy controls were asked to perform digit recall accompanied by a secondary tracking task. Individuals who were carriers of the genetic mutation demonstrated significantly higher dual task costs than healthy non-carriers. Dual task performance was found to be more sensitive to this very early stage of FAD than episodic memory measures. The findings support the notion that a deficit in the coordination mechanism of the central executive may be a pre-clinical marker for the early detection of AD due to the E280A presenilin-1 gene mutation.
先前的双重任务研究表明,与健康对照组相比,散发性阿尔茨海默病(AD)患者在同时执行两项任务的能力上存在障碍,尽管他们能够相对较好地单独成功完成这些任务。然而,目前尚不清楚这种双重任务协调缺陷的最早临床表现是什么。本研究检查了由于 E280A 早发型家族性 AD 早发性 AD 风险的个体的双重任务能力。由于 E280A 早发型家族性 AD 基因突变,有 39 名基因突变携带者未达到 AD 标准,29 名非携带者健康对照组被要求进行数字回忆并伴有次要跟踪任务。携带基因突变的个体的双重任务成本明显高于健康非携带者。与情景记忆测量相比,双重任务表现对 FAD 的这个非常早期阶段更为敏感。研究结果支持这样一种观点,即中央执行协调机制的缺陷可能是由于 E280A 早发型家族性 AD 基因突变导致 AD 早期检测的临床前标志物。