Boluda Susana, Toledo Jon B, Irwin David J, Raible Kevin M, Byrne Matt D, Lee Edward B, Lee Virginia M-Y, Trojanowski John Q
Department of Pathology and Laboratory Medicine, Center for Neurodegenerative Disease Research, Institute on Aging, University of Pennsylvania School of Medicine, Philadelphia, PA, 19104, USA.
Acta Neuropathol. 2014 Oct;128(4):543-50. doi: 10.1007/s00401-014-1308-9. Epub 2014 Jun 12.
Current neuropathological Alzheimer's disease (AD) criteria from the National Institute on Aging-Alzheimer's Association (NIA-AA) incorporate two staging systems for Aβ pathology, namely the Thal Aβ phase (TAP) and the Consortium to Establish a Registry for Alzheimer's Disease (CERAD) methods. The goal of this study was to compare and contrast results obtained with these two different staging systems for Aβ pathology since this is critical for future correlations of Aβ amyloid imaging data with Aβ neuropathology data based on immunohistochemical detection of Aβ deposits. A total of 123 cases, divided into 82 training and 41 validation cases, with a diagnosis of either unremarkable adult brain (normal) or AD and CERAD scores ranging from none to frequent were included. There was no clear and consistent relationship between CERAD and the TAP Aβ scores with the exception of scores for the highest plaque burdens (i.e., CERAD C3 and TAP A3) in the cases studied here. However, we developed an algorithm that relates CERAD scores to TAP scores with high agreement (94 % in training and 98 % in the validation set). In addition, TAP scores were a better predictor of dementia (sensitivity of 94 % specificity 87.7 %) than CERAD scores (sensitivity of 57 % specificity 100 %). Yet, further research is needed to define strategies to relate CERAD and TAP Aβ plaque scores to compare their utility and for determining the clinical associations of these different amyloid staging systems with aging and AD.
美国国立衰老研究所-阿尔茨海默病协会(NIA-AA)现行的阿尔茨海默病(AD)神经病理学标准纳入了两种Aβ病理学分期系统,即Thal Aβ分期(TAP)和阿尔茨海默病注册协会(CERAD)方法。本研究的目的是比较和对比这两种不同Aβ病理学分期系统所获得的结果,因为这对于未来基于Aβ沉积物免疫组化检测的Aβ淀粉样蛋白成像数据与Aβ神经病理学数据的相关性至关重要。总共纳入了123例病例,分为82例训练病例和41例验证病例,诊断为成人脑无异常(正常)或AD,CERAD评分从无到频繁。除了此处研究病例中最高斑块负荷的评分(即CERAD C3和TAP A3)外,CERAD和TAP Aβ评分之间没有明确且一致的关系。然而,我们开发了一种算法,该算法能将CERAD评分与TAP评分高度一致地关联起来(训练集为94%,验证集为98%)。此外,与CERAD评分(敏感性为57%,特异性为100%)相比,TAP评分是痴呆症更好的预测指标(敏感性为94%,特异性为87.7%)。然而,仍需要进一步研究来确定将CERAD和TAP Aβ斑块评分相关联的策略,以比较它们的效用,并确定这些不同淀粉样蛋白分期系统与衰老和AD的临床关联。