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脊髓小脑性共济失调 2 型患者社会认知障碍的神经生物学基础。

The neurobiological underpinning of the social cognition impairments in patients with spinocerebellar ataxia type 2.

机构信息

Department of Psychology, Sapienza University, Rome, Italy; Ataxia Laboratory, Fondazione Santa Lucia IRCCS, Rome, Italy.

Department of Psychology, Sapienza University, Rome, Italy; Ataxia Laboratory, Fondazione Santa Lucia IRCCS, Rome, Italy.

出版信息

Cortex. 2021 May;138:101-112. doi: 10.1016/j.cortex.2020.12.027. Epub 2021 Feb 13.

Abstract

Clinical studies described emotional and social behaviour alterations in patients with cerebellar diseases, proposing a role of specific cerebello-cerebral circuits in social cognition. However, for a long time these difficulties were underestimated, and no studies have addressed the correlation between social cognition deficits and topography of the cerebellar damage. The present study aims to investigate the social cognition impairment and the neuroanatomical alterations in patients with spinocerebellar ataxia type 2 (SCA2) and to analyze their relationship. To this purpose a social cognition battery composed by three tests, and a MRI protocol were administered to 13 SCA2 patients and 26 healthy subjects. The pattern of gray matter (GM) atrophy was analyzed by voxel-based morphometry, and the GM volumes of each altered area were correlated with the behavioral scores to investigate anatomo-functional relationships. In addition, we investigated the relationship between social deficits and damage to the cerebellar peduncles using DTI diffusivity indices. Our patients showed impairment of the immediate perceptual component of the mental state recognition (i.e., to recognize feelings and thoughts from the eyes expression), and difficulties in anger attribution, and in the understanding of false or mistaken beliefs. They showed a pattern of GM reduction in cerebellar regions, including lobules IX and VIIIb and Crus II, all of which are involved in specific components of the mentalizing process. Interestingly, the behavioral performance, in which SCA2 patients showed impairments compared to controls, correlated with the degree of cerebellar GM reduction and with the presence of microstructural abnormalities in the cerebellar peduncles. The present study provides the first characterization of the social cognition deficits in a homogenous cohort SCA2 patients and demonstrates that alterations in specific cerebellar regions should represent the neurobiological underpinning of their social behavior difficulties. Our results offer a new point of view in considering these aspects in the clinical practice.

摘要

临床研究描述了小脑疾病患者的情绪和社交行为改变,提出了特定的小脑-大脑回路在社交认知中的作用。然而,很长一段时间以来,这些困难都被低估了,没有研究探讨社交认知缺陷与小脑损伤的拓扑结构之间的相关性。本研究旨在调查脊髓小脑性共济失调 2 型(SCA2)患者的社交认知障碍和神经解剖改变,并分析它们之间的关系。为此,我们对 13 名 SCA2 患者和 26 名健康受试者进行了社交认知测试组合和 MRI 方案。通过基于体素的形态计量学分析灰质(GM)萎缩模式,并将每个改变区域的 GM 体积与行为评分相关联,以研究解剖-功能关系。此外,我们还使用弥散张量成像(DTI)扩散指数研究了社交缺陷与小脑脚损伤之间的关系。我们的患者表现出即时感知心理状态识别的能力受损(即,从眼睛表情识别感觉和想法),并且在愤怒归因、理解虚假或错误信念方面存在困难。他们表现出小脑区域的 GM 减少模式,包括小叶 IX 和 VIIIb 和 Crus II,所有这些区域都参与了心理化过程的特定成分。有趣的是,与对照组相比,SCA2 患者表现出行为障碍的程度与小脑 GM 减少的程度以及小脑脚存在微观结构异常相关。本研究首次对同质 SCA2 患者队列的社交认知缺陷进行了特征描述,并证明了特定小脑区域的改变应该代表其社交行为困难的神经生物学基础。我们的研究结果为在临床实践中考虑这些方面提供了一个新的视角。

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