Cairns Nigel J, Perrin Richard J, Franklin Erin E, Carter Deborah, Vincent Benjamin, Xie Mingqiang, Bateman Randall J, Benzinger Tammie, Friedrichsen Karl, Brooks William S, Halliday Glenda M, McLean Catriona, Ghetti Bernardino, Morris John C
Knight Alzheimer's Disease Research Center, Washington University School of Medicine, St. Louis, Missouri, USA.
Department of Neurology, Washington University School of Medicine, St. Louis, Missouri, USA.
Neuropathology. 2015 Aug;35(4):390-400. doi: 10.1111/neup.12205. Epub 2015 May 12.
It has been hypothesized that the relatively rare autosomal dominant Alzheimer disease (ADAD) may be a useful model of the more frequent, sporadic, late-onset AD (LOAD). Individuals with ADAD have a predictable age at onset and the biomarker profile of ADAD participants in the preclinical stage may be used to predict disease progression and clinical onset. However, the extent to which the pathogenesis and neuropathology of ADAD overlaps with that of LOAD is equivocal. To address this uncertainty, two multicenter longitudinal observational studies, the Alzheimer Disease Neuroimaging Initiative (ADNI) and the Dominantly Inherited Alzheimer Network (DIAN), leveraged the expertise and resources of the existing Knight Alzheimer Disease Research Center (ADRC) at Washington University School of Medicine, St. Louis, Missouri, USA, to establish a Neuropathology Core (NPC). The ADNI/DIAN-NPC is systematically examining the brains of all participants who come to autopsy at the 59 ADNI sites in the USA and Canada and the 14 DIAN sites in the USA (eight), Australia (three), UK (one) and Germany (two). By 2014, 41 ADNI and 24 DIAN autopsies (involving nine participants and 15 family members) had been performed. The autopsy rate in the ADNI cohort in the most recent year was 93% (total since NPC inception: 70%). In summary, the ADNI/DIAN NPC has implemented a standard protocol for all sites to solicit permission for brain autopsy and to send brain tissue to the NPC for a standardized, uniform and state-of-the-art neuropathologic assessment. The benefit to ADNI and DIAN of the implementation of the NPC is very clear. The NPC provides final "gold standard" neuropathological diagnoses and data against which the antecedent observations and measurements of ADNI and DIAN can be compared.
据推测,相对罕见的常染色体显性阿尔茨海默病(ADAD)可能是更常见的散发性晚发性阿尔茨海默病(LOAD)的有用模型。ADAD患者有可预测的发病年龄,临床前期ADAD参与者的生物标志物特征可用于预测疾病进展和临床发病。然而,ADAD的发病机制和神经病理学与LOAD的重叠程度尚不清楚。为了解决这一不确定性,两项多中心纵向观察研究,即阿尔茨海默病神经影像学倡议(ADNI)和显性遗传阿尔茨海默病网络(DIAN),利用了美国密苏里州圣路易斯华盛顿大学医学院现有奈特阿尔茨海默病研究中心(ADRC)的专业知识和资源,建立了一个神经病理学核心(NPC)。ADNI/DIAN-NPC正在系统地检查在美国和加拿大的59个ADNI站点以及美国(8个)、澳大利亚(3个)、英国(1个)和德国(2个)的14个DIAN站点进行尸检的所有参与者的大脑。到2014年,已进行了41例ADNI和24例DIAN尸检(涉及9名参与者和15名家庭成员)。ADNI队列中最近一年的尸检率为93%(自NPC成立以来的总尸检率:70%)。总之,ADNI/DIAN NPC已为所有站点实施了一项标准方案,以征求脑尸检许可,并将脑组织送往NPC进行标准化、统一和先进的神经病理学评估。NPC的实施对ADNI和DIAN的益处非常明显。NPC提供最终的“金标准”神经病理学诊断和数据,可与ADNI和DIAN先前的观察和测量结果进行比较。