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静息运动阈与阿尔茨海默病的严重程度相关吗?

Does Resting Motor Threshold correlate with severity of Alzheimer's disease?

出版信息

Annu Int Conf IEEE Eng Med Biol Soc. 2022 Jul;2022:4383-4386. doi: 10.1109/EMBC48229.2022.9871657.

Abstract

Conflicting results have emerged from studies examining the potential of resting motor threshold (RMT) as a neurophysiological marker for Alzheimer's disease (AD) diagnosis and progression. In this study, we estimated the strength of the association between RMT measurements and severity of cognitive impairment in a relatively large sample (N=128) of clinical trial participants with mild (Clinical Dementia Rating - CDR=1) to moderate (CDR=2) AD. RMT for each participant was determined by applying single-pulse transcranial magnetic stimulation repeated at varying intensities over left and right sides of the primary motor cortex. RMT is the minimum intensity that evoked a visible contralateral involuntary finger twitch and RMT asymmetry is the absolute difference between the left and right RMT measurements. Cognitive impairment was measured with the Montreal Cognitive Assessment (MoCA) and the Alzheimer Disease Assessment Scale - Cognitive (ADAS-Cog) scores. Although the left and right RMT was lower in CDR 2 than in CDR 1 participants, neither RMT nor RMT asymmetry correlated significantly with cognitive test scores. In conclusion, our study in a large sample size does not support the idea that RMT is a sensitive marker of cognitive decline/severity in AD. Clinical Relevance- This study provides evidence that RMT may not be useful for AD progression monitoring.

摘要

研究表明,静息运动阈值(RMT)作为阿尔茨海默病(AD)诊断和进展的神经生理学标志物存在相互矛盾的结果。在这项研究中,我们在一个相对较大的临床试验参与者样本(N=128)中,评估了 RMT 测量值与认知障碍严重程度之间的关联强度,这些参与者的 AD 为轻度(临床痴呆评定量表 - CDR=1)至中度(CDR=2)。每位参与者的 RMT 通过在初级运动皮层的左右两侧以不同强度重复施加单次脉冲经颅磁刺激来确定。RMT 是引起可见对侧无意识手指抽搐的最小强度,RMT 不对称性是左右 RMT 测量值之间的绝对差异。认知障碍通过蒙特利尔认知评估(MoCA)和阿尔茨海默病评估量表 - 认知(ADAS-Cog)评分来衡量。尽管 CDR 2 参与者的左右 RMT 低于 CDR 1 参与者,但 RMT 或 RMT 不对称性与认知测试评分均无显著相关性。总之,我们在大样本量中的研究不支持 RMT 是 AD 认知衰退/严重程度的敏感标志物的观点。临床意义 - 这项研究提供了证据表明 RMT 可能不适用于 AD 进展监测。

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