TY - JOUR
T1 - Neuropathologic assessment of participants in two multi-center longitudinal observational studies
T2 - The Alzheimer Disease Neuroimaging Initiative (ADNI) and the Dominantly Inherited Alzheimer Network (DIAN)
AU - the Alzheimer Disease Neuroimaging Initiative and the Dominantly Inherited Alzheimer Network
AU - Cairns, Nigel J.
AU - Perrin, Richard J.
AU - Franklin, Erin E.
AU - Carter, Deborah
AU - Vincent, Benjamin
AU - Xie, Mingqiang
AU - Bateman, Randall J.
AU - Benzinger, Tammie
AU - Friedrichsen, Karl
AU - Brooks, William S.
AU - Halliday, Glenda M.
AU - Mclean, Catriona
AU - Ghetti, Bernardino
AU - Morris, John C.
N1 - Publisher Copyright:
© 2015 Japanese Society of Neuropathology.
PY - 2015/8/1
Y1 - 2015/8/1
N2 - 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.
AB - 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.
KW - Autosomal dominant Alzheimer disease
KW - Late-onset Alzheimer disease
KW - Neuropathologic diagnostic criteria
KW - Neuropathologic heat map
KW - PET-PiB amyloid imaging
UR - http://www.scopus.com/inward/record.url?scp=84934291197&partnerID=8YFLogxK
U2 - 10.1111/neup.12205
DO - 10.1111/neup.12205
M3 - Article
C2 - 25964057
AN - SCOPUS:84934291197
SN - 0919-6544
VL - 35
SP - 390
EP - 400
JO - Neuropathology
JF - Neuropathology
IS - 4
ER -