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特发性快速眼动睡眠行为障碍的皮质变薄模式。

Patterns of cortical thinning in idiopathic rapid eye movement sleep behavior disorder.

作者信息

Rahayel Shady, Montplaisir Jacques, Monchi Oury, Bedetti Christophe, Postuma Ronald B, Brambati Simona, Carrier Julie, Joubert Sven, Latreille Véronique, Jubault Thomas, Gagnon Jean-François

机构信息

Centre for Advanced Research in Sleep Medicine, Hôpital du Sacré-Coeur de Montréal, Montreal, Quebec, Canada; Department of Psychology, Université du Québec à Montréal, Montreal, Quebec, Canada.

出版信息

Mov Disord. 2015 Apr 15;30(5):680-7. doi: 10.1002/mds.25820. Epub 2014 Feb 22.

Abstract

Idiopathic rapid eye movement sleep behavior disorder is a parasomnia that is a risk factor for dementia with Lewy bodies and Parkinson's disease. Brain function impairments have been identified in this disorder, mainly in the frontal and posterior cortical regions. However, the anatomical support for these dysfunctions remains poorly understood. We investigated gray matter thickness, gray matter volume, and white matter integrity in patients with idiopathic rapid eye movement sleep behavior disorder. Twenty-four patients with polysomnography-confirmed idiopathic rapid eye movement sleep behavior disorder and 42 healthy individuals underwent a 3-tesla structural and diffusion magnetic resonance imaging examination using corticometry, voxel-based morphometry, and diffusion tensor imaging. In the patients with idiopathic rapid eye movement sleep behavior disorder, decreased cortical thickness was observed in the frontal cortex, the lingual gyrus, and the fusiform gyrus. Gray matter volume was reduced in the superior frontal sulcus only. Patients showed no increased gray matter thickness or volume. Diffusion tensor imaging analyses revealed no significant white matter differences between groups. Using corticometry in patients with idiopathic rapid eye movement sleep behavior disorder, several new cortical regions with gray matter alterations were identified, similar to those reported in dementia with Lewy bodies and Parkinson's disease. These findings provide some anatomical support for previously identified brain function impairments in this disorder.

摘要

特发性快速眼动睡眠行为障碍是一种异态睡眠,是路易体痴呆和帕金森病的危险因素。已在该疾病中发现脑功能损害,主要位于额叶和后皮质区域。然而,对这些功能障碍的解剖学支持仍知之甚少。我们研究了特发性快速眼动睡眠行为障碍患者的灰质厚度、灰质体积和白质完整性。24例经多导睡眠图确诊的特发性快速眼动睡眠行为障碍患者和42名健康个体接受了3特斯拉结构和扩散磁共振成像检查,采用皮质测量法、基于体素的形态测量法和扩散张量成像。在特发性快速眼动睡眠行为障碍患者中,观察到额叶皮质、舌回和梭状回的皮质厚度降低。仅额上沟的灰质体积减少。患者未出现灰质厚度或体积增加。扩散张量成像分析显示两组之间白质无显著差异。使用皮质测量法对特发性快速眼动睡眠行为障碍患者进行研究,发现了几个新的灰质改变的皮质区域,类似于路易体痴呆和帕金森病中报道的区域。这些发现为该疾病中先前确定的脑功能损害提供了一些解剖学支持。

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