TY - JOUR
T1 - A public resource of baseline data from the Alzheimer's Prevention Initiative Autosomal-Dominant Alzheimer's Disease Trial
AU - and the API ADAD Colombia Trial Group
AU - Reiman, Eric M.
AU - Pruzin, Jeremy J.
AU - Rios-Romenets, Silvia
AU - Brown, Chris
AU - Giraldo, Margarita
AU - Acosta-Baena, Natalia
AU - Tobon, Carlos
AU - Hu, Nan
AU - Chen, Yinghua
AU - Ghisays, Valentina
AU - Enos, Jessica
AU - Goradia, Dhruman D.
AU - Lee, Wendy
AU - Luo, Ji
AU - Malek-Ahmadi, Michael
AU - Protas, Hillary
AU - Thomas, Ronald G.
AU - Chen, Kewei
AU - Su, Yi
AU - Boker, Connie
AU - Mastroeni, Diego
AU - Alvarez, Sergio
AU - Quiroz, Yakeel T.
AU - Langbaum, Jessica B.
AU - Sink, Kaycee M.
AU - Lopera, Francisco
AU - Tariot, Pierre N.
N1 - Funding Information:
The Alzheimer's Prevention Initiative (API) was established in 2008 to accelerate the evaluation of promising prevention therapies in persons at increased risk for Alzheimer's disease (AD) and provide a shared resource of prevention trial data and biological samples. The API Autosomal‐Dominant Alzheimer's Disease (ADAD) Prevention Trial (NCT01998841) received grant support from the National Institutes of Health (NIH) as part of the 2012 National Plan to Address Alzheimer's Disease, introducing novel pre‐clinical AD prevention strategies that have been embraced and extended by both academia and industry to evaluate AD‐modifying treatments in persons at genetic and/or biomarker risk for the disease. The API ADAD Trial is intended to be potentially license‐enabling, support the development of theragnostic biomarkers that could further accelerate the evaluation and approval of prevention therapies, and establish public–private partnerships to support this endeavor. The API ADAD Trial included a commitment to provide a public resource of data and biological samples after trial completion. 1–7 7
Funding Information:
This paper was made possible by Grants RF1AG041705, R01AG055444, and P30AG072980 from the National Institute on Aging (NIA). Its contents are solely the responsibility of the authors and do not necessarily represent the official views of the NIH/NIA. The API ADAD Trial is a public–private partnership led by researchers from Banner Alzheimer's Institute, the Grupo Neurociencias de Antioquia (GNA; part of the University of Antioquia and the main study site for the API ADAD Trial), Genentech/Roche, and the NIA. The API ADAD Trial is supported by the above mentioned NIA grants, Genentech and its parent organization Roche, and generous philanthropic contributions to the Banner Alzheimer's Foundation. The API ADAD Trial and its related programs have been supported by Banner Alzheimer's Foundation, NOMIS Foundation, FIL/Fidelity Bermuda Foundation, Flinn Foundation, and Colciencias. The authors would like to thank their valued research participants and families; current and former colleagues in the API ADAD Trial; and our collaborators from DIAN, the A4 Trials Program, and CAP for exchanging information about policies and procedures to share data and samples in ways that provide appropriate participant and trial protections.
Publisher Copyright:
© 2022 The Authors. Alzheimer's & Dementia published by Wiley Periodicals LLC on behalf of Alzheimer's Association.
PY - 2022
Y1 - 2022
N2 - Introduction: The Alzheimer's Prevention Initiative Autosomal-Dominant Alzheimer's Disease (API ADAD) Trial evaluated the anti-oligomeric amyloid beta (Aβ) antibody therapy crenezumab in cognitively unimpaired members of the Colombian presenilin 1 (PSEN1) E280A kindred. We report availability, methods employed to protect confidentiality and anonymity of participants, and process for requesting and accessing baseline data. Methods: We developed mechanisms to share baseline data from the API ADAD Trial in consultation with experts and other groups sharing data from Alzheimer's disease (AD) prevention trials, balancing the need to protect anonymity and trial integrity with making data broadly available to accelerate progress in the field. We pressure-tested deliberate and inadvertent potential threats under specific assumptions, employed a system to suppress or mask both direct and indirect identifying variables, limited and firewalled data managers, and put forth specific principles requisite to receive data. Results: Baseline demographic, PSEN1 E280A and apolipoprotein E genotypes, florbetapir and fluorodeoxyglucose positron emission tomography, magnetic resonance imaging, clinical, and cognitive data can now be requested by interested researchers. Discussion: Baseline data are publicly available; treatment data and biological samples, including baseline and treatment-related blood-based biomarker data will become available in accordance with our original trial agreement and subsequently developed Collaboration for Alzheimer's Prevention principles. Sharing of these data will allow exploration of important questions including the differential effects of initiating an investigational AD prevention therapy both before as well as after measurable Aβ plaque deposition.
AB - Introduction: The Alzheimer's Prevention Initiative Autosomal-Dominant Alzheimer's Disease (API ADAD) Trial evaluated the anti-oligomeric amyloid beta (Aβ) antibody therapy crenezumab in cognitively unimpaired members of the Colombian presenilin 1 (PSEN1) E280A kindred. We report availability, methods employed to protect confidentiality and anonymity of participants, and process for requesting and accessing baseline data. Methods: We developed mechanisms to share baseline data from the API ADAD Trial in consultation with experts and other groups sharing data from Alzheimer's disease (AD) prevention trials, balancing the need to protect anonymity and trial integrity with making data broadly available to accelerate progress in the field. We pressure-tested deliberate and inadvertent potential threats under specific assumptions, employed a system to suppress or mask both direct and indirect identifying variables, limited and firewalled data managers, and put forth specific principles requisite to receive data. Results: Baseline demographic, PSEN1 E280A and apolipoprotein E genotypes, florbetapir and fluorodeoxyglucose positron emission tomography, magnetic resonance imaging, clinical, and cognitive data can now be requested by interested researchers. Discussion: Baseline data are publicly available; treatment data and biological samples, including baseline and treatment-related blood-based biomarker data will become available in accordance with our original trial agreement and subsequently developed Collaboration for Alzheimer's Prevention principles. Sharing of these data will allow exploration of important questions including the differential effects of initiating an investigational AD prevention therapy both before as well as after measurable Aβ plaque deposition.
KW - Alzheimer's disease
KW - amyloid
KW - antibody
KW - data sharing
KW - magnetic resonance imaging
KW - positron emission tomography
KW - presenilin 1
KW - primary prevention
KW - secondary prevention
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U2 - 10.1002/alz.12843
DO - 10.1002/alz.12843
M3 - Article
C2 - 36373344
AN - SCOPUS:85143266115
JO - Alzheimer's and Dementia
JF - Alzheimer's and Dementia
SN - 1552-5260
ER -