Can MRI Visual Assessment Differentiate the Variants of Primary-Progressive Aphasia?

被引:22
作者
Sajjadi, S. A. [1 ]
Sheikh-Bahaei, N. [2 ,3 ]
Cross, J. [3 ]
Gillard, J. H. [2 ,3 ]
Scoffings, D. [3 ]
Nestor, P. J. [4 ]
机构
[1] Univ Calif Irvine, Dept Neurol, Irvine, CA 92717 USA
[2] Univ Cambridge, Dept Radiol, Cambridge, England
[3] Cambridge Univ Hosp, Dept Radiol, Cambridge, England
[4] German Ctr Neurodegenerat Dis, Magdeburg, Germany
关键词
FRONTOTEMPORAL LOBAR DEGENERATION; VOXEL-BASED MORPHOMETRY; SEMANTIC DEMENTIA; ALZHEIMERS-DISEASE; CONNECTED SPEECH; VOLUMETRIC MRI; ATROPHY; PATTERNS; CLASSIFICATION; SEGMENTATION;
D O I
10.3174/ajnr.A5126
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND AND PURPOSE: Primary-progressive aphasia is a clinically and pathologically heterogeneous condition. Nonfluent, semantic, and logopenic are the currently recognized clinical variants. The recommendations for the classification of primary-progressive aphasia have advocated variant-specific patterns of atrophy. The aims of the present study were to evaluate the sensitivity and specificity of the proposed imaging criteria and to assess the intra- and interrater reporting agreements. MATERIALS AND METHODS: The cohort comprised 51 patients with a root diagnosis of primary-progressive aphasia, 25 patients with typical Alzheimer disease, and 26 matched control participants. Group-level analysis (voxel-based morphometry) confirmed the proposed atrophy patterns for the 3 syndromes. The individual Tl-weighted anatomic images were reported by 3 senior neuroradiologists. RESULTS: We observed a dichotomized pattern of high sensitivity (92%) and specificity (93%) for the proposed atrophy pattern of semantic-variant primary-progressive aphasia and low sensitivity (21% for nonfluent-variant primary-progressive aphasia and 43% for' logopenic-variant primary-progressive aphasia) but high specificity (91% for nonfluent-variant primary-progressive aphasia and 95% for logopenic-variant primary-progressive aphasia) in other primary-progressive aphasia variants and Alzheimer disease (sensitivity 43%, specificity 92%). MR imaging was least sensitive for the diagnosis of nonfluent-variant primary-progressive aphasia. intrarater agreement analysis showed mean K values above the widely accepted threshold of 0.6 (mean, 0.63 +/- 0.16). Pair-wise interobserver agreement outcomes, however, were well below this threshold in 5 of the 6 possible interrater contrasts (mean, 0.41 +/- 0.09). CONCLUSIONS: While the group-level results were in precise agreement with the recommendations, semantic-variant primary-progressive aphasia was the only subtype for which the proposed recommendations were both sensitive and specific at an individual level.
引用
收藏
页码:954 / 960
页数:7
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