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不同类型肌萎缩侧索硬化症和进行性延髓麻痹的额区参与:Stroop 事件相关电位和反应时研究

Different Frontal Involvement in ALS and PLS Revealed by Stroop Event-Related Potentials and Reaction Times.

机构信息

Neurological Department, Institute of Experimental Neurology (INSPE), Scientific Institute Hospital San Raffaele, University Vita-Salute San Raffaele , Milan , Italy.

出版信息

Front Aging Neurosci. 2013 Dec 12;5:82. doi: 10.3389/fnagi.2013.00082. eCollection 2013.

Abstract

BACKGROUND

A growing body of evidence suggests a link between cognitive and pathological changes in amyotrophic lateral sclerosis (ALS) and in frontotemporal lobar degeneration (FTLD). Cognitive deficits have been investigated much less extensively in primary lateral sclerosis (PLS) than in ALS.

OBJECTIVE

To investigate bioelectrical activity to Stroop test, assessing frontal function, in ALS, PLS, and control groups.

METHODS

Thirty-two non-demented ALS patients, 10 non-demented PLS patients, and 27 healthy subjects were included. Twenty-nine electroencephalography channels with binaural reference were recorded during covert Stroop task performance, involving mental discrimination of the stimuli and not vocal or motor response. Group effects on event-related potentials (ERPs) latency were analyzed using statistical multivariate analysis. Topographic analysis was performed using low-resolution brain electromagnetic tomography (LORETA).

RESULTS

Amyotrophic lateral sclerosis patients committed more errors in the execution of the task but they were not slower, whereas PLS patients did not show reduced accuracy, despite a slowing of reaction times (RTs). The main ERP components were delayed in ALS, but not in PLS, compared with controls. Moreover, RTs speed but not ERP latency correlated with clinical scores. ALS had decreased frontotemporal activity in the P2, P3, and N4 time windows compared to controls.

CONCLUSION

These findings suggest a different pattern of psychophysiological involvement in ALS compared with PLS. The former is increasingly recognized to be a multisystems disorder, with a spectrum of executive and behavioral impairments reflecting frontotemporal dysfunction. The latter seems to mainly involve the motor system, with largely spared cognitive functions. Moreover, our results suggest that the covert version of the Stroop task used in the present study, may be useful to assess cognitive state in the very advanced stage of the disease, when other cognitive tasks are not applicable.

摘要

背景

越来越多的证据表明,肌萎缩侧索硬化症(ALS)和额颞叶变性(FTLD)的认知和病理变化之间存在联系。与 ALS 相比,原发性侧索硬化症(PLS)的认知缺陷研究得要少得多。

目的

研究 ALS、PLS 和对照组在 Stroop 测试中的生物电活动,评估额叶功能。

方法

纳入 32 名非痴呆 ALS 患者、10 名非痴呆 PLS 患者和 27 名健康对照者。在执行隐蔽 Stroop 任务期间,记录了 29 个带有双耳参考的脑电图通道,该任务涉及对刺激的心理辨别,而不是发声或运动反应。使用统计多变量分析对组间事件相关电位(ERP)潜伏期的影响进行分析。使用低分辨率脑电磁层析成像(LORETA)进行地形图分析。

结果

与对照组相比,ALS 患者在执行任务时犯了更多的错误,但他们的反应速度并不慢,而 PLS 患者的反应速度虽然较慢,但准确性并没有降低。与对照组相比,ALS 的主要 ERP 成分延迟,但 PLS 则没有。此外,反应时间(RT)速度而非 ERP 潜伏期与临床评分相关。与对照组相比,ALS 在 P2、P3 和 N4 时间窗口的额颞叶活动减少。

结论

这些发现表明,与 PLS 相比,ALS 的心理生理受累模式不同。前者越来越被认为是一种多系统疾病,具有一系列执行和行为障碍,反映了额颞叶功能障碍。后者似乎主要涉及运动系统,而认知功能则基本不受影响。此外,我们的研究结果表明,本研究中使用的隐蔽 Stroop 任务可能有助于在疾病的晚期评估认知状态,因为其他认知任务不适用于该阶段。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c329/3860257/d7d75277e247/fnagi-05-00082-g001.jpg

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