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淀粉样蛋白阴性的进行性非流畅性原发性进行性失语的临床和神经影像学生物标志物

Clinical and neuroimaging biomarkers of amyloid-negative logopenic primary progressive aphasia.

作者信息

Whitwell Jennifer L, Duffy Joseph R, Strand Edythe A, Machulda Mary M, Senjem Matthew L, Schwarz Christopher G, Reid Robert, Baker Matthew C, Perkerson Ralph B, Lowe Val J, Rademakers Rosa, Jack Clifford R, Josephs Keith A

机构信息

Department of Radiology, Mayo Clinic, Rochester, MN, United States.

Department of Neurology (Division of Speech Pathology), Mayo Clinic, Rochester, MN, United States.

出版信息

Brain Lang. 2015 Mar;142:45-53. doi: 10.1016/j.bandl.2015.01.009. Epub 2015 Feb 3.

Abstract

Logopenic primary progressive aphasia (lvPPA) is a progressive language disorder characterized by anomia, difficulty repeating complex sentences, and phonological errors. The majority, although not all, lvPPA patients have underlying Alzheimer's disease. We aimed to determine whether clinical or neuroimaging features differ according to the deposition of Aβ on Pittsburgh-compound B PET in lvPPA. Clinical features, patterns of atrophy on MRI, hypometabolism on FDG-PET, and white matter tract degeneration were compared between six PiB-negative and 20 PiB-positive lvPPA patients. PiB-negative patients showed more asymmetric left-sided patterns of atrophy, hypometabolism and white matter tract degeneration, with greater left anteromedial temporal and medial prefrontal involvement, than PiB-positive patients. PiB-positive patients showed greater involvement of right temporoparietal and frontal lobes. There was very little evidence for clinical differences between the groups. Strikingly asymmetric neuroimaging findings with relatively preserved right hemisphere may provide clues that AD pathology is absent in lvPPA.

摘要

语义性原发性进行性失语(lvPPA)是一种进行性语言障碍,其特征为命名障碍、重复复杂句子困难以及语音错误。大多数(并非全部)lvPPA患者患有潜在的阿尔茨海默病。我们旨在确定根据匹兹堡化合物B正电子发射断层扫描(PET)上β淀粉样蛋白(Aβ)的沉积情况,lvPPA患者的临床或神经影像学特征是否存在差异。对6例匹兹堡化合物B阴性和20例匹兹堡化合物B阳性的lvPPA患者的临床特征、磁共振成像(MRI)上的萎缩模式、氟代脱氧葡萄糖正电子发射断层扫描(FDG-PET)上的代谢减低以及白质束变性进行了比较。与匹兹堡化合物B阳性患者相比,匹兹堡化合物B阴性患者表现出更不对称的左侧萎缩、代谢减低和白质束变性模式,左侧前内侧颞叶和内侧前额叶受累更明显。匹兹堡化合物B阳性患者右侧颞顶叶和额叶受累更明显。两组之间几乎没有临床差异的证据。具有相对保留的右半球的明显不对称神经影像学表现可能提供线索,表明lvPPA中不存在阿尔茨海默病病理。

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