Abstract
We aimed to evaluate the value of ATN biomarker classification system (amyloid beta [A], pathologic tau [T], and neurodegeneration [N]) for predicting conversion from mild cognitive impairment (MCI) to dementia. In a sample of people with MCI (n = 415) we assessed predictive performance of ATN classification using empirical knowledge-based cut-offs for each component of ATN and compared it to two data-driven approaches, logistic regression and RUSBoost machine learning classifiers, which used continuous clinical or biomarker scores. In data-driven approaches, we identified ATN features that distinguish normals from individuals with dementia and used them to classify persons with MCI into dementia-like and normal groups. Both data-driven classification methods performed better than the empirical cut-offs for ATN biomarkers in predicting conversion to dementia. Classifiers that used clinical features performed as well as classifiers that used ATN biomarkers for prediction of progression to dementia. We discuss that data-driven modeling approaches can improve our ability to predict disease progression and might have implications in future clinical trials.
Original language | English (US) |
---|---|
Pages (from-to) | 1855-1867 |
Number of pages | 13 |
Journal | Alzheimer's and Dementia |
Volume | 17 |
Issue number | 11 |
DOIs | |
State | Published - Nov 2021 |
Keywords
- Alzheimer's disease
- amyloid
- biomarker profile
- machine learning
- mild cognitive impairment
- neurodegeneration
- predictive analytics
- tau
ASJC Scopus subject areas
- Epidemiology
- Health Policy
- Developmental Neuroscience
- Clinical Neurology
- Geriatrics and Gerontology
- Cellular and Molecular Neuroscience
- Psychiatry and Mental health
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In: Alzheimer's and Dementia, Vol. 17, No. 11, 11.2021, p. 1855-1867.
Research output: Contribution to journal › Article › peer-review
}
TY - JOUR
T1 - Predictive value of ATN biomarker profiles in estimating disease progression in Alzheimer's disease dementia
AU - The Alzheimer's Disease Neuroimaging Initiative
AU - Ezzati, Ali
AU - Abdulkadir, Ahmed
AU - Jack, Clifford R.
AU - Thompson, Paul M.
AU - Harvey, Danielle J.
AU - Truelove-Hill, Monica
AU - Sreepada, Lasya P.
AU - Davatzikos, Christos
AU - Lipton, Richard B.
N1 - Funding Information: Data collection and sharing for the ADNI project was funded by the Alzheimer's Disease Neuroimaging Initiative (ADNI; National Institutes of Health Grant U01 AG024904) and DOD ADNI (Department of Defense award number W81XWH-12-2-0012). ADNI is funded by the National Institute on Aging, the National Institute of Biomedical Imaging and Bioengineering, and through generous contributions from the following: AbbVie; Alzheimer's Association; Alzheimer's Drug Discovery Foundation; Araclon Biotech; BioClinica, Inc.; Biogen; Bristol-Myers Squibb Company; CereSpir, Inc.; Cogstate; Eisai Inc.; Elan Pharmaceuticals, Inc.; Eli Lilly and Company; EuroImmun; F. Hoffmann-La Roche Ltd and its affiliated company Genentech, Inc.; Fujirebio; GE Healthcare; IXICO Ltd.; Janssen Alzheimer Immunotherapy Research & Development, LL.; Johnson & Johnson Pharmaceutical Research & Development LLC; Lumosity; Lundbeck; Merck & Co., Inc.; Meso Scale Diagnostics, LLC; NeuroRx Research; Neurotrack Technologies; Novartis Pharmaceuticals Corporation; Pfizer Inc.; Piramal Imaging; Servier; Takeda Pharmaceutical Company; and Transition Therapeutics. The Canadian Institutes of Health Research is providing funds to support ADNI clinical sites in Canada. Private sector contributions are facilitated by the Foundation for the National Institutes of Health (www.fnih.org). The grantee organization is the Northern California Institute for Research and Education, and the study is coordinated by the Alzheimer's Therapeutic Research Institute at the University of Southern California. ADNI data are disseminated by the Laboratory for Neuro Imaging at the University of Southern California. Authors of this study were supported by grants from the National Institute of Health (NIA K23 AG063993 [A.E]; P01-AG003949 [R.B.]); P41 EB015922, U01 AG024904, P01 AG026572, P01 AG055367, R56 AG058854, RF1 AG051710 (P.M.T); U01 AG024904 [P.M.T and C.D.]); the Alzheimer's Association (2019-AACSF-641329; A.E.); Cure Alzheimer Fund (A.E. & R.B.L.), the Leonard and Sylvia Marx Foundation (R.B.L.). Sponsors played no role. Funding Information: Data collection and sharing for the ADNI project was funded by the Alzheimer's Disease Neuroimaging Initiative (ADNI; National Institutes of Health Grant U01 AG024904) and DOD ADNI (Department of Defense award number W81XWH‐12‐2‐0012). ADNI is funded by the National Institute on Aging, the National Institute of Biomedical Imaging and Bioengineering, and through generous contributions from the following: AbbVie; Alzheimer's Association; Alzheimer's Drug Discovery Foundation; Araclon Biotech; BioClinica, Inc.; Biogen; Bristol‐Myers Squibb Company; CereSpir, Inc.; Cogstate; Eisai Inc.; Elan Pharmaceuticals, Inc.; Eli Lilly and Company; EuroImmun; F. Hoffmann‐La Roche Ltd and its affiliated company Genentech, Inc.; Fujirebio; GE Healthcare; IXICO Ltd.; Janssen Alzheimer Immunotherapy Research & Development, LL.; Johnson & Johnson Pharmaceutical Research & Development LLC; Lumosity; Lundbeck; Merck & Co., Inc.; Meso Scale Diagnostics, LLC; NeuroRx Research; Neurotrack Technologies; Novartis Pharmaceuticals Corporation; Pfizer Inc.; Piramal Imaging; Servier; Takeda Pharmaceutical Company; and Transition Therapeutics. The Canadian Institutes of Health Research is providing funds to support ADNI clinical sites in Canada. Private sector contributions are facilitated by the Foundation for the National Institutes of Health ( www.fnih.org ). The grantee organization is the Northern California Institute for Research and Education, and the study is coordinated by the Alzheimer's Therapeutic Research Institute at the University of Southern California. ADNI data are disseminated by the Laboratory for Neuro Imaging at the University of Southern California. Authors of this study were supported by grants from the National Institute of Health (NIA K23 AG063993 [A.E]; P01‐AG003949 [R.B.]); P41 EB015922, U01 AG024904, P01 AG026572, P01 AG055367, R56 AG058854, RF1 AG051710 (P.M.T); U01 AG024904 [P.M.T and C.D.]); the Alzheimer's Association (2019‐AACSF‐641329; A.E.); Cure Alzheimer Fund (A.E. & R.B.L.), the Leonard and Sylvia Marx Foundation (R.B.L.). Sponsors played no role. Funding Information: Ali Ezzati has served on the advisory board of Eisai. Ahmed Abdulkadir has received research support from Swiss National Science Foundation and served as an external expert for the European Research Commission. Clifford R. Jack Jr. has research support from NIH unrelated to this manuscript and serves on advisory boards for Biogen, Eisai, and Roche. Paul M. Thompson is supported in part by a research grant from Biogen, Inc. (Boston, USA) for research unrelated to this manuscript. He receives consulting fees from Kairos Venture Capital, Inc. Danielle J. Harvey receives research support as a biostatistician from the following sources unrelated to this manuscript: NIH: P30 AG010129, U54 NS079202, R01 AG048252, R01 AG029672, R01 AG051618, R01 HD093654, UH2/UH3 NS100608, R01 AG062240, R01 AG062689, R01 AG064688, 2U54 HD079125; DoD: W81XWH‐13‐1‐0259, W81XWH‐12‐2‐0012, W81XWH‐14‐1‐0462; California Department of Public Health: 1910611‐0. Monica Truelove‐Hill has nothing to disclose. Lasya P. Sreepada has nothing to disclose. Christos Davatzikos receives research support from the following sources unrelated to this manuscript: NIH: R01NS042645, R01MH112070, R01NS042645, U24CA189523; and medical legal consulting work unrelated to this paper. Richard B. Lipton receives research support from the following sources unrelated to this manuscript: NIH: 2PO1 AG003949 (mPI), 5U10 NS077308 (PI), R21 AG056920 (Investigator), 1RF1 AG057531 (Site PI), RF1 AG054548 (Investigator), 1RO1 AG048642 (Investigator), R56 AG057548 (Investigator), U01062370 (Investigator), RO1 AG060933 (Investigator), RO1 AG062622 (Investigator), 1UG3FD006795 (mPI), 1U24NS113847 (Investigator), K23 NS09610 (Mentor), K23AG049466 (Mentor), K23 NS107643 (Mentor). He also receives support from the Migraine Research Foundation and the National Headache Foundation. He serves on the editorial board of , is senior advisor to , and associate editor to . He has reviewed for the NIA and NINDS; holds stock options in eNeura Therapeutics and Biohaven Holdings; serves as consultant, advisory board member, or has received honoraria from: Abbvie (Allergan), American Academy of Neurology, American Headache Society, Amgen, Avanir, Biohaven, Biovision, Boston Scientific, Dr. Reddy's (Promius), Electrocore, Eli Lilly, eNeura Therapeutics, Equinox, GlaxoSmithKline, Grifols, Lundbeck (Alder), Merck, Pernix, Pfizer, Supernus, Teva, Trigemina, Vector, Vedanta. He receives royalties from Wolff's 7th and 8th editions, Oxford Press University, 2009, Wiley, and Informa. He receives consulting fees from Impel NeuroPharma and Novartis and has stock or options in Control M. Neurology Headache Cephalalgia Headache Publisher Copyright: © 2021 the Alzheimer's Association
PY - 2021/11
Y1 - 2021/11
N2 - We aimed to evaluate the value of ATN biomarker classification system (amyloid beta [A], pathologic tau [T], and neurodegeneration [N]) for predicting conversion from mild cognitive impairment (MCI) to dementia. In a sample of people with MCI (n = 415) we assessed predictive performance of ATN classification using empirical knowledge-based cut-offs for each component of ATN and compared it to two data-driven approaches, logistic regression and RUSBoost machine learning classifiers, which used continuous clinical or biomarker scores. In data-driven approaches, we identified ATN features that distinguish normals from individuals with dementia and used them to classify persons with MCI into dementia-like and normal groups. Both data-driven classification methods performed better than the empirical cut-offs for ATN biomarkers in predicting conversion to dementia. Classifiers that used clinical features performed as well as classifiers that used ATN biomarkers for prediction of progression to dementia. We discuss that data-driven modeling approaches can improve our ability to predict disease progression and might have implications in future clinical trials.
AB - We aimed to evaluate the value of ATN biomarker classification system (amyloid beta [A], pathologic tau [T], and neurodegeneration [N]) for predicting conversion from mild cognitive impairment (MCI) to dementia. In a sample of people with MCI (n = 415) we assessed predictive performance of ATN classification using empirical knowledge-based cut-offs for each component of ATN and compared it to two data-driven approaches, logistic regression and RUSBoost machine learning classifiers, which used continuous clinical or biomarker scores. In data-driven approaches, we identified ATN features that distinguish normals from individuals with dementia and used them to classify persons with MCI into dementia-like and normal groups. Both data-driven classification methods performed better than the empirical cut-offs for ATN biomarkers in predicting conversion to dementia. Classifiers that used clinical features performed as well as classifiers that used ATN biomarkers for prediction of progression to dementia. We discuss that data-driven modeling approaches can improve our ability to predict disease progression and might have implications in future clinical trials.
KW - Alzheimer's disease
KW - amyloid
KW - biomarker profile
KW - machine learning
KW - mild cognitive impairment
KW - neurodegeneration
KW - predictive analytics
KW - tau
UR - http://www.scopus.com/inward/record.url?scp=85120854274&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85120854274&partnerID=8YFLogxK
U2 - 10.1002/alz.12491
DO - 10.1002/alz.12491
M3 - Article
C2 - 34870371
AN - SCOPUS:85120854274
SN - 1552-5260
VL - 17
SP - 1855
EP - 1867
JO - Alzheimer's and Dementia
JF - Alzheimer's and Dementia
IS - 11
ER -