神经病理学
萎缩
心理学
原发性进行性失语
失语症
阿尔茨海默病
正电子发射断层摄影术
疾病
生物标志物
认知
听力学
认知功能衰退
痴呆
神经科学
医学
病理
失智症
化学
生物化学
作者
Adam Martersteck,Jaiashre Sridhar,Christina Coventry,Sandra Weıntraub,Marsel Mesulam,Emily Rogalskı
摘要
Abstract Introduction Examination of pathologic, anatomic, and cognitive relationships has been limited in primary progressive aphasia (PPA) with underlying Alzheimer's disease (AD) neuropathology. Methods Spatial relationships between tau positron emission tomography (PET), cortical thickness, age, and naming on the Boston Naming Test (BNT) in PPA with biomarker evidence of AD (PPA‐AD) were examined. Results Higher tau PET burden was associated with atrophy and younger age. There was a significant left‐lateralized relationship between lower BNT and more atrophy, and between lower BNT and increased tau burden. Variance in naming was primarily shared between tau and atrophy (51%), but naming was uniquely explained more by atrophy (32%) than tau (16%). Higher left anterior temporal tau burden was associated with greater 1‐year rate of decline in naming. Discussion PPA‐AD has a similar relationship between abnormal biomarkers as first described in amnestic AD, with differing spatial extent, reflecting the left‐lateralized nature of the language network.
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