Chenery Helen J, Copland David A, Murdoch Bruce E
Department of Speech Pathology and Audiology, University of Queensland, Australia.
Int J Lang Commun Disord. 2002 Oct-Dec;37(4):459-74. doi: 10.1080/1368282021000007730.
The neuropathological changes associated with Huntington's disease (HD) are most marked in the head of the caudate nucleus and, to a lesser extent, in the putamen and globus pallidus, suggesting that at least part of the language impairments found in patients with HD may result from non-thalamic subcortical (NTS) pathology. The present study aimed to test the hypothesis that a signature profile of impaired language functions is found in patients who have sustained damage to the non-thalamic subcortex, either focally induced or resulting from neurodegenerative pathology. The language abilities of a group of patients with Huntington's disease (n=13) were compared with those of an age- and education-matched group of patients with chronic NTS lesions following stroke (n=13) and a non-neurologically impaired control group (n=13). The three groups were compared on language tasks that assessed both primary and more complex language abilities. The primary language battery consisted of The Western Aphasia Battery and The Boston Naming Test, whilst the more complex cognitive-linguistic battery employed selected subtests from The Test of Language Competence - Expanded, The Test of Word Knowledge and The Word Test - Revised. On many of the tests of primary language function from the Western Aphasia Battery, both the HD and NTS participants performed in a similar manner to the control participants. The language performances of the HD participants were significantly more impaired (p<0.05 using modified Bonferroni adjustments) than the control group, however, on various lexico-semantic tasks (e.g. the Boston Naming Test and providing definitions), on both single-word and sentence-level generative tasks (e.g. category fluency and formulating sentences), and on tasks which required interpretation of ambiguous, figurative and inferential meaning. The difficulties that patients with HD experienced with tasks assessing complex language abilities were strikingly similar, both qualitatively and quantitatively, to the language profile produced by NTS participants. The results provide evidence to suggest that a signature language profile is associated with damage to the non-thalamic subcortex resulting from either focal neurological insult or a degenerative disease.
与亨廷顿舞蹈症(HD)相关的神经病理学变化在尾状核头部最为显著,在壳核和苍白球的变化程度稍轻,这表明HD患者出现的至少部分语言障碍可能是由非丘脑皮质下(NTS)病变引起的。本研究旨在验证以下假设:在因局灶性损伤或神经退行性病变而导致非丘脑皮质下受损的患者中,可发现语言功能受损的特征性表现。将一组亨廷顿舞蹈症患者(n = 13)的语言能力与年龄和教育程度相匹配的中风后慢性NTS病变患者组(n = 13)以及无神经功能障碍的对照组(n = 13)进行比较。在评估主要和更复杂语言能力的语言任务上对这三组进行比较。主要语言测试组合包括西方失语症测试组合和波士顿命名测试,而更复杂的认知语言测试组合则采用了语言能力测试 - 扩展版、词汇知识测试和单词测试 - 修订版中的选定子测试。在西方失语症测试组合的许多主要语言功能测试中,HD组和NTS组参与者的表现与对照组参与者相似。然而,在各种词汇语义任务(如波士顿命名测试和给出定义)、单字和句子层面的生成任务(如类别流畅性和造句)以及需要解释模糊、比喻和推理意义的任务上,HD组参与者的语言表现明显比对照组受损更严重(使用修正的邦费罗尼校正,p < 0.05)。HD组患者在评估复杂语言能力任务上遇到的困难在质量和数量上都与NTS组参与者产生的语言特征惊人地相似。结果提供了证据表明,由局灶性神经损伤或退行性疾病导致的非丘脑皮质下损伤与特征性语言表现相关。