Henley Susie M D, Wild Edward J, Hobbs Nicola Z, Warren Jason D, Frost Chris, Scahill Rachael I, Ridgway Gerard R, MacManus David G, Barker Roger A, Fox Nick C, Tabrizi Sarah J
Dementia Research Centre, Institute of Neurology, University College London, UK.
Neuropsychologia. 2008;46(8):2152-60. doi: 10.1016/j.neuropsychologia.2008.02.025. Epub 2008 Mar 6.
Huntington's disease (HD) is an inherited neurodegenerative disorder that classically presents with motor, cognitive and psychiatric symptoms. However, other abnormalities also occur in this condition, notably deficient recognition of facial emotional expressions. Deficits in emotion recognition impact significantly on the lives of HD patients and their families and thus it is important to clarify the onset and pattern of impairment. This study investigated facial emotion recognition in a large cohort of early HD patients, and premanifest gene-carriers. We used voxel-based morphometry (VBM) to examine the neuroanatomical correlates of emotion recognition performance. Forty patients with early HD, 21 premanifest gene carriers and 20 controls were assessed using 24 faces from the Ekman Pictures of Facial Affect, and volumetric brain MRI. The HD group was significantly worse than controls at recognising, surprise, disgust, anger and fear, and worse than the premanifest group at recognising disgust and anger. When patient data were expressed as z-scores, recognition of anger was significantly worse than disgust in the early HD group. In the VBM analysis, these deficits were associated with common regional atrophy: impaired recognition of surprise, disgust, anger and fear were all associated with striatal volume loss. Fear was associated with additional atrophy of the right insula and left and right lateral orbitofrontal cortex. Even in early HD there is a wide-ranging impairment in recognition of negative emotions denoting 'threat'. Our findings implicate a generic fronto-subcortical network in the pathogenesis of these emotion recognition deficits.
亨廷顿舞蹈症(HD)是一种遗传性神经退行性疾病,典型症状包括运动、认知和精神症状。然而,这种疾病还会出现其他异常情况,尤其是面部情绪表情识别能力不足。情绪识别缺陷对HD患者及其家人的生活产生重大影响,因此明确损伤的发作和模式很重要。本研究调查了一大群早期HD患者和症状前基因携带者的面部情绪识别情况。我们使用基于体素的形态测量法(VBM)来检查情绪识别表现的神经解剖学相关性。使用来自艾克曼面部表情图片的24张面孔和脑部容积MRI对40名早期HD患者、21名症状前基因携带者和20名对照者进行了评估。HD组在识别惊讶、厌恶、愤怒和恐惧方面明显比对照组差,在识别厌恶和愤怒方面比症状前组差。当将患者数据表示为z分数时,早期HD组中愤怒的识别明显比厌恶差。在VBM分析中,这些缺陷与常见的区域萎缩有关:惊讶、厌恶、愤怒和恐惧识别受损均与纹状体体积减小有关。恐惧还与右侧岛叶以及左侧和右侧眶额外侧皮质的额外萎缩有关。即使在早期HD中,对表示“威胁”的负面情绪的识别也存在广泛损伤。我们的研究结果表明,一个通用的额颞叶皮质下网络在这些情绪识别缺陷的发病机制中起作用。