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特发性全面性癫痫中听觉注意力处理的选择性损伤:对其认知病理生理学的影响。

Selective impairment of auditory attention processing in idiopathic generalized epilepsies: Implications for their cognitive pathophysiology.

机构信息

Department of Neurosurgery, Epilepsy Surgery Unit, School of Medicine, Evangelismos Hospital, National and Kapodistrian University of Athens, Athens, Greece.

Department of Technologies, Communication and Society, University of Rome G. Marconi, Rome, Italy.

出版信息

Appl Neuropsychol Adult. 2022 Sep-Oct;29(5):1131-1140. doi: 10.1080/23279095.2020.1852566. Epub 2020 Dec 7.

Abstract

The neuropsychological characteristics of Idiopathic Generalized Epilepsies (IGEs) as a wide syndrome encompassing different clinical entities have been as yet not well understood. We have studied neuropsychological performance in patients suffering Juvenile Myoclonic Epilepsy (JME) and Generalized Tonic Clonic Seizures (IGE-GTCS-only) to provide indirect-cognitive evidence on the pathophysiology of IGE-related neuropsychological dysfunction. Greater arousal-related impairments were expected for the auditory modality, by drawing on previous anatomo-clinical and neuro-evolutionary accounts. We have studied neurocognitive functioning in 26 IGE patients, suffering either JME ( = 16) or IGE-GTCS-only ( = 10), and their healthy counterparts consisted of 26 (18 females) demographically matched participants. IGE patients (JME and IGE-GTCS-only) did worse with respect to HC (healthy controls) in visual- and auditory- speed of information processing (reaction time), auditory-vigilance and -response inhibition, visuo-motor coordination, visual working memory and motor speed, delayed visual recall, immediate- and delayed verbal episodic recall, lexical access and retrieval, semantic associative processing, auditory-verbal memory span and verbal learning. Although both IGE-GTCS-only and JME patients delayed episodic recall was defective, the former did significantly worse. We believe that IGE patients' neuropsychological derailments represent indirect-secondary manifestations of a primary cortical tone deregulation inherent to IGEs' pathophysiology. In particular, IGE patients' worse-dissociated performance in auditory TOVA-also seen previously in TBI and schizophrenia-may implicate a grater vulnerability of the auditory information processing system, as well as a possibly shared cognitive pathophysiological component between IGE and the above nosologies.

摘要

特发性全面性癫痫(IGE)作为一个广泛的综合征,包含不同的临床实体,其神经心理学特征迄今尚未得到很好的理解。我们研究了患有青少年肌阵挛性癫痫(JME)和全面强直阵挛发作(IGE-GTCS 仅)的患者的神经心理学表现,以提供与 IGE 相关神经心理功能障碍的病理生理学的间接认知证据。以前的解剖临床和神经进化研究表明,人们预计听觉模式的唤醒相关损伤会更大。我们研究了 26 名 IGE 患者的神经认知功能,其中 16 名患有 JME,10 名患有 IGE-GTCS 仅,他们的健康对照组由 26 名(18 名女性)在人口统计学上匹配的参与者组成。与 HC(健康对照组)相比,IGE 患者(JME 和 IGE-GTCS 仅)在视觉和听觉信息处理速度(反应时间)、听觉警觉性和反应抑制、视动协调、视觉工作记忆和运动速度、延迟视觉回忆、即时和延迟词语情节回忆、词汇访问和检索、语义联想加工、听觉词语记忆广度和词语学习方面表现更差。尽管 IGE-GTCS 仅和 JME 患者的情节回忆均有缺陷,但前者的表现明显更差。我们认为,IGE 患者的神经心理障碍代表了 IGE 病理生理学中固有皮质紧张调节原发性障碍的间接继发性表现。特别是,IGE 患者在听觉 TOVA 中的表现更差,这在 TBI 和精神分裂症中也有发现,这可能意味着听觉信息处理系统的脆弱性更大,以及 IGE 和上述分类学之间可能存在共同的认知病理生理成分。

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