F33 Task-switching abilities in pre-manifest huntington’s disease subjects

S. Migliore, Giulia D'Aurizio, Sabrina Maffi, G. Curcio, F. Squitieri
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Abstract

Background Huntington’s Disease (HD) cognitive dysfunction may start before unequivocal motor signs become apparent. Main early cognitive abnormal domains may include deficits in psychomotor speed, negative emotion recognition and executive functioning. Previous studies have demonstrated an impaired performance in several frontal tasks in HD patients. Aim The present study aimed to investigate the executive control of cognition in pre-manifest (pre) HD subjects, by means of a task-switching protocol. Methods We enrolled 30 preHD subjects (DCL<4) that were subsequently assigned to two experimental groups: 15 to the preHD1 group (with a Total Motor Score-TMS ≤ 4) and 15 to the preHD2 group (with a 5 ≤TMS≤ 9). Their performance was compared with a group of 18 healthy controls (HC). Two different tasks were performed in rapid and random succession, so that the task was either changed from one trial to the next one (switch trials) or repeated (repetition trials). Switch trials are usually slower than repetitions, causing a so-called switch cost (SC). Results preHD subjects showed slower reaction times than HC in both switch (pre-HD2: 1201.133±19.99; pre-HD 1: 1099.7±15.76; HC: 755.61±12.63; p<0.0001) and repetition trials (pre-HD2: 920.8±14.90; pre-HD1: 895.5±14.13; HC: 683.97±10.74; p=0.001), as also confirmed by a significantly increased SC (pre-HD2: 360.98±7.98; pre-HD1: 192.84±10.32; HC: 76.56±7.98; p=0.01). More specifically, preHD2 subjects showed a significantly impaired switching ability characterized by slower reaction times compared with both preHD1 and HC. Conclusions The executive control is impaired before HD becomes manifest. Such abnormalities worsen in preHD subjects with first subtle motor features that are still insufficient and unspecific to document the onset. Considering that such abilities have obvious implication with behavior and independence, the beneficial effect of early rehabilitation programs focused on executive function should be tested.
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F33显前亨廷顿病受试者的任务转换能力
背景:亨廷顿氏病(HD)的认知功能障碍可能在明确的运动体征变得明显之前就开始了。早期认知异常主要包括精神运动速度缺陷、负性情绪识别缺陷和执行功能缺陷。先前的研究表明,HD患者在几个额叶任务中的表现受损。目的通过任务切换协议,探讨HD前显(前)被试的认知执行控制。方法将30例DCL<4的preHD受试者分为两个实验组:15例preHD1组(总运动评分-TMS≤4)和15例preHD2组(5≤TMS≤9),并与18例健康对照组(HC)进行比较。两个不同的任务以快速和随机的顺序进行,因此任务要么从一个试验切换到下一个试验(切换试验),要么重复(重复试验)。切换试验通常比重复慢,导致所谓的切换成本(SC)。结果pre- hd组在两个开关上的反应时间均低于HC组(pre-HD2: 1201.133±19.99;预高清1:10 99.7±15.76;HC: 755.61±12.63;p<0.0001)和重复试验(pre-HD2: 920.8±14.90;pre-HD1: 895.5±14.13;HC: 683.97±10.74;p=0.001), SC也显著升高(hd2前:360.98±7.98;pre-HD1: 192.84±10.32;HC: 76.56±7.98;p = 0.01)。更具体地说,与preHD1和HC相比,preHD2受试者表现出明显的转换能力受损,其特征是反应时间较慢。结论HD发病前执行控制功能受损。这种异常在hd前患者中恶化,伴有最初的细微运动特征,这些特征仍然不足以证明发病。考虑到这些能力对行为和独立性有明显的影响,应该测试早期执行功能康复计划的有益效果。
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WED 253 An atypical presentation of sneddon syndrome H29 Practical tools and transfer aids in daily care for clients with advanced hd F06 When and how does manifest hd begin? a comparison of age at onset of motor and non-motor symptoms F33 Task-switching abilities in pre-manifest huntington’s disease subjects F56 Psychiatric symptoms in huntington’s disease: relationship to disease stage in the CAPIT-HD2 beta-testing study
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