Sajjadi S A, Sheikh-Bahaei N, Cross J, Gillard J H, Scoffings D, Nestor P J
From the Department of Neurology (S.A.S.), University of California, Irvine, Irvine, California
Department of Radiology (N.S.-B., J.H.G.), University of Cambridge, Cambridge, UK.
AJNR Am J Neuroradiol. 2017 May;38(5):954-960. doi: 10.3174/ajnr.A5126. Epub 2017 Mar 24.
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.
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 T1-weighted anatomic images were reported by 3 senior neuroradiologists.
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 κ 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).
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.
原发性进行性失语是一种临床和病理表现均异质性的疾病。非流利型、语义型和音韵型是目前公认的临床变异型。原发性进行性失语的分类建议主张采用变异型特异性萎缩模式。本研究的目的是评估所提出的影像学标准的敏感性和特异性,并评估阅片者内部和阅片者之间的报告一致性。
该队列包括51例原发性进行性失语确诊患者、25例典型阿尔茨海默病患者和26例匹配的对照参与者。组水平分析(基于体素的形态测量)证实了3种综合征所提出的萎缩模式。3位资深神经放射科医生报告了个体的T1加权解剖图像。
我们观察到,对于语义变异型原发性进行性失语所提出的萎缩模式,呈现出高敏感性(92%)和特异性(93%)的二分模式;而在其他原发性进行性失语变异型和阿尔茨海默病中(敏感性43%,特异性92%),非流利变异型原发性进行性失语的敏感性较低(21%),音韵变异型原发性进行性失语的敏感性为43%,但特异性较高(非流利变异型原发性进行性失语为91%,音韵变异型原发性进行性失语为95%)。磁共振成像对非流利变异型原发性进行性失语的诊断敏感性最低。阅片者内部一致性分析显示,平均κ值高于广泛接受的0.6阈值(平均值,0.63±0.16)。然而,在6种可能的阅片者间对比中,有5种的两两阅片者间一致性结果远低于该阈值(平均值,0.41±0.09)。
虽然组水平结果与建议完全一致,但语义变异型原发性进行性失语是所提出的建议在个体水平上既敏感又特异的唯一亚型。