Louwersheimer Eva, Keulen M Antoinette, Steenwijk Martijn D, Wattjes Mike P, Jiskoot Lize C, Vrenken Hugo, Teunissen Charlotte E, van Berckel Bart N M, van der Flier Wiesje M, Scheltens Philip, van Swieten John C, Pijnenburg Yolande A L
Alzheimer Center and Department of Neurology, Neuroscience Campus Amsterdam, VU University Medical Center, Amsterdam, The Netherlands.
MS Center Amsterdam and Department of Radiology and Nuclear Medicine, Neuroscience campus Amsterdam, VU University Medical Center, Amsterdam, The Netherlands.
J Alzheimers Dis. 2016;51(2):581-90. doi: 10.3233/JAD-150812.
The logopenic variant of Primary Progressive Aphasia (lvPPA) is associated with underlying Alzheimer's disease (AD) pathology and characterized by impaired single word retrieval and repetition of phrases and sentences.
We set out to study whether logopenic aphasia is indeed the prototypic language profile in PPA patients with biomarker evidence of underlying AD pathology and to correlate language profiles with cortical atrophy patterns on MRI.
Inclusion criteria: (I) clinical diagnosis of PPA; (II) CSF profile and/or PiB-PET scan indicative for amyloid pathology; (III) availability of expert language evaluation. Based on language evaluation, patients were classified as lvPPA (fulfilling lvPPA core criteria), lvPPA extended (fulfilling core criteria plus other language disturbances), or PPA unclassifiable (not fulfilling lvPPA core criteria). Cortical atrophy patterns on MRI were visually rated and quantitative measurements of cortical thickness were performed using FreeSurfer.
We included 22 patients (age 67±7 years, 50% female, MMSE 21±6). 41% were classified as lvPPA, 36% as lvPPA extended with additional deficits in language comprehension and/or confrontation naming, and 23% as PPA unclassifiable. By both qualitative and quantitative measurements, patients with lvPPA showed mild global cortical atrophy on MRI, whereas patients with lvPPA extended showed more focal cortical atrophy, predominantly at the left tempo-parietal side. For PPA unclassifiable, qualitative measurements revealed a heterogeneous atrophy pattern.
Although most patients fulfilled the lvPPA criteria, we found that their language profiles were heterogeneous. The clinical and radiological spectrum of PPA due to underlying AD pathology is broader than pure lvPPA.
原发性进行性失语的语音迟缓变异型(lvPPA)与潜在的阿尔茨海默病(AD)病理相关,其特征为单个词检索受损以及短语和句子复述障碍。
我们旨在研究语音迟缓性失语是否确实是具有潜在AD病理生物标志物证据的PPA患者的典型语言特征,并将语言特征与MRI上的皮质萎缩模式相关联。
纳入标准:(I)PPA的临床诊断;(II)脑脊液检查结果和/或PiB-PET扫描提示淀粉样蛋白病理;(III)可获得专家语言评估。根据语言评估,患者被分类为lvPPA(符合lvPPA核心标准)、扩展型lvPPA(符合核心标准加其他语言障碍)或无法分类的PPA(不符合lvPPA核心标准)。对MRI上的皮质萎缩模式进行视觉评分,并使用FreeSurfer进行皮质厚度的定量测量。
我们纳入了22例患者(年龄67±7岁,50%为女性,简易精神状态检查表21±6)。41%被分类为lvPPA,36%为扩展型lvPPA,伴有语言理解和/或对答命名方面的额外缺陷,23%为无法分类的PPA。通过定性和定量测量,lvPPA患者在MRI上显示轻度全脑皮质萎缩,而扩展型lvPPA患者显示更局灶性的皮质萎缩,主要位于左侧颞顶叶。对于无法分类的PPA,定性测量显示萎缩模式异质性。
尽管大多数患者符合lvPPA标准,但我们发现他们的语言特征是异质性的。由潜在AD病理导致的PPA的临床和放射学谱比单纯的lvPPA更广泛。