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Identification of an atypical variant of logopenic progressive aphasia

机译:确定非典型性渐进性失语症

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The purpose of this study was to examine the association between aphasia severity and neurocognitive function, disease duration and temporoparietal atrophy in 21 individuals with the logopenic variant of primary progressive aphasia (lvPPA). We found significant correlations between aphasia severity and degree of neurocognitive impairment as well as temporoparietal atrophy; but not disease duration. Cluster analysis identified three variants of lvPPA: (1) subjects with mild aphasia and short disease duration (mild typical lvPPA); (2) subjects with mild aphasia and long disease duration (mild atypical lvPPA); and, (3) subjects with severe aphasia and relatively long disease duration (severe typical lvPPA). All three variants showed temporoparietal atrophy, with the mild atypical group showing the least atrophy despite the longest disease duration. The mild atypical group also showed mild neuropsychological impairment. The subjects with mild aphasia and neuropsychological impairment despite long disease duration may represent a slowly progressive variant of lvPPA.
机译:这项研究的目的是检查失语症严重程度与神经认知功能,疾病持续时间和颞顶萎缩之间的关联,其中有21位患有原发性渐进性失语症(LVPPA)的人。我们发现失语症严重程度与神经认知障碍程度以及颞顶萎缩之间存在显着相关性。但疾病持续时间却没有。聚类分析确定了lvPPA的三种变体:(1)轻度失语症和病程短(轻度典型lvPPA)的受试者; (2)患有轻度失语症且病程长(轻度非典型lvPPA)的受试者; (3)患有严重失语症且病程较长的受试者(严重的典型lvPPA)。这三种变体均表现为颞顶萎缩,尽管病程最长,轻度非典型组的萎缩最少。轻度非典型组也显示轻度神经心理障碍。尽管疾病持续时间长,但患有轻度失语和神经心理障碍的受试者可能代表了lvPPA的缓慢进行性变异。

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