Grossman Murray, McMillan Corey, Moore Peachie, Ding Lijun, Glosser Guila, Work Melissa, Gee James
Department of Neurology, University of Pennsylvania, 3400 Spruce Street, Philadelphia, PA 19104-4283, USA.
Brain. 2004 Mar;127(Pt 3):628-49. doi: 10.1093/brain/awh075. Epub 2004 Feb 4.
Confrontation naming is impaired in neurodegenerative conditions like Alzheimer's disease (AD), frontotemporal dementia (FTD) and corticobasal degeneration (CBD). Some behavioural observations suggest a common source of impaired naming across these patient groups, while others find partially unique patterns of naming difficulty. We hypothesized that a large-scale neural network underlies naming, and that patterns of impaired naming in AD, FTD and CBD reflect cortical atrophy that interrupts this network in a manner that is partially shared and partially unique across these patient groups. We tested this hypothesis by correlating naming impairments with voxel-based morphometric (VBM) analyses of cortical atrophy in structural MRIs of 50 patients. We found significant naming deficits in all patient groups. Naming also correlated with lexical retrieval in all patient groups, including subgroups of patients with FTD. VBM analyses showed significant cortical atrophy, which was shared across AD, FTD and CBD patients in the left lateral temporal cortex; this area correlated with naming accuracy in all groups. Left lateral temporal atrophy thus appears to interfere with a lexical retrieval component of naming in AD, FTD and CBD. Impaired naming also correlated with semantic memory and visual perceptual-spatial functioning in specific groups of patients and, correspondingly, naming correlated with cortical atrophy in partially distinct neuroanatomical distributions in AD, FTD, CBD and subgroups of patients with FTD. These partially unique correlation profiles appear to reflect selective interruption of other components of the naming process, including semantic and visual perceptual-spatial functioning. These findings are consistent with the hypothesis that a large-scale neural network supports naming, and that this network is interrupted in several distinct ways in patients with neurodegenerative diseases.
在诸如阿尔茨海默病(AD)、额颞叶痴呆(FTD)和皮质基底节变性(CBD)等神经退行性疾病中,对物体命名的能力会受损。一些行为观察表明,这些患者群体中命名受损存在共同根源,而另一些研究则发现了部分独特的命名困难模式。我们假设存在一个大规模神经网络支撑着命名功能,并且AD、FTD和CBD患者中命名受损的模式反映了皮质萎缩,这种萎缩以部分共享且部分独特的方式中断了该网络,在这些患者群体中表现各异。我们通过将50名患者的结构磁共振成像(MRI)中基于体素的形态测量(VBM)分析与命名损伤进行关联,来检验这一假设。我们发现所有患者组均存在显著的命名缺陷。在所有患者组中,包括FTD患者亚组,命名也与词汇检索相关。VBM分析显示存在显著的皮质萎缩,AD、FTD和CBD患者在左侧颞叶外侧皮质存在共同的萎缩区域;该区域与所有组的命名准确性相关。因此,左侧颞叶外侧萎缩似乎会干扰AD、FTD和CBD患者命名中的词汇检索成分。在特定患者组中,命名受损还与语义记忆和视觉感知空间功能相关,相应地,在AD、FTD、CBD以及FTD患者亚组中,命名与部分不同神经解剖分布区域的皮质萎缩相关。这些部分独特的相关性特征似乎反映了命名过程中其他成分的选择性中断,包括语义和视觉感知空间功能。这些发现与以下假设一致:一个大规模神经网络支撑着命名功能,并且在神经退行性疾病患者中,这个网络以几种不同的方式被中断。