路易体痴呆(DLB)与帕金森病痴呆(PDD)患者定量脑电图(q-EEG)测量的比较

Mehrnaz Rezvanfard, Ali Khaleghi, Amirhossein Ghaderi, Maryam Noroozian, Vajiheh Aghamollaii, Mehdi Tehranidust
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引用次数: 0

摘要

路易体痴呆(DLB)和帕金森病痴呆(PDD)是具有相似症状特征的突触核蛋白病综合征,临床根据症状发作时间的任意规则进行区分。确定可靠的脑电图(EEG)生物标志物将为更好地诊断、治疗和监测这两种痴呆症的治疗反应提供一种精确的方法。回顾性分析2015年4月至2021年3月间某神经内科门诊的新转诊记录,选取28例DLB(70.3%男性)和20例PDD(80.8%男性)符合EEG的患者作为研究对象。采用EEGLAB对60 s无伪影的21通道闭眼静息脑电信号进行分析,提取区域谱功率比。与PDD患者相比,DLB患者在所有区域都有明显的弥漫性减慢,α波段减少,θ波段增加。虽然在调整MMSE评分后,这些发现在两组之间有所降低,但在平均相对alpha功率方面仍然存在显著差异,特别是在前部和中央区域。QEEG测量可能有可能区分这两种综合征。然而,需要进一步的前瞻性和纵向研究来改善这些痴呆综合征的早期鉴别,并阐明其潜在的病因和发病机制以及具体的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of Quantitative-Electroencephalogram (q-EEG) Measurements Between Patients of Dementia with Lewy Bodies (DLB) and Parkinson Disease Dementia (PDD).

Dementia with Lewy bodies (DLB) and Parkinson's disease dementia (PDD) are synucleinopathy syndromes with similar symptom profiles that are distinguished clinically based on the arbitrary rule of the time of symptom onset. Identifying reliable electroencephalographic (EEG) biomarkers would provide a precise method for better diagnosis, treatment, and monitoring of treatment response in these two types of dementia. From April 2015 to March 2021, the records of new referrals to a neurology clinic were retrospectively reviewed and 28 DLB(70.3% male) and 20 PDD (80.8% male) patients with appropriate EEG were selected for this study. Artifact-free 60-s EEG signals (21 channels) at rest with eyes closed were analyzed using EEGLAB, and regional spectral power ratios were extracted. Marked diffuse slowing was found in DLB patients compared to PDD patients in all regions in terms of decrease in alpha and increase in theta band. Although, these findings demean between groups after adjusting for MMSE scores, the significant difference still remained in terms of the mean relative alpha powers, particularly in the anterior and central regions. QEEG measures may have the potential to discriminate between these two syndromes. However, further prospective and longitudinal studies are required to improve the early differentiation of these dementia syndromes and to elucidate the underlying causes and pathogenesis and specific treatment.

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