The Alzheimer's Disease Neuroimaging Initiative in the era of Alzheimer's disease treatment: A review of ADNI studies from 2021 to 2022
Open accessAbstract
The Alzheimer's Disease Neuroimaging Initiative (ADNI) aims to improve Alzheimer's disease (AD) clinical trials. Since 2006, ADNI has shared clinical, neuroimaging, and cognitive data, and biofluid samples. We used conventional search methods to identify 1459 publications from 2021 to 2022 using ADNI data/samples and reviewed 291 impactful studies. This review details how ADNI studies improved disease progression understanding and clinical trial efficiency. Advances in subject selection, detection of treatment effects, harmonization, and modeling improved clinical trials and plasma biomarkers like phosphorylated tau showed promise for clinical use. Biomarkers of amyloid beta, tau, neurodegeneration, inflammation, and others were prognostic with individualized prediction algorithms available online. Studies supported the amyloid cascade, emphasized the importance of neuroinflammation, and detailed widespread heterogeneity in disease, linked to genetic and vascular risk, co-pathologies, sex, and resilience. Biological subtypes were consistently observed. Generalizability of ADNI results is limited by lack of cohort diversity, an issue ADNI-4 aims to address by enrolling a diverse cohort.
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Predictive signatures derived from ADNI datasets often underperform in community-based cohorts that differ in ancestry, education level, and comorbid conditions.
“Predictive signatures derived from ADNI datasets often underperform in community-based cohorts that differ in ancestry, education level, and comorbid conditions259.”
From Artificial intelligence-driven multi-omics approaches in Alzheimer's disease: Progress, challenges, and future directions (2025) · cites this paper as [259]
In “Diagnosis and prediction approaches” (page unavailable), the review reports that ADNI-developed MRI classifiers performed less well in external memory-clinic cohorts, and that a score tested in the more diverse ARIC cohort performed differently across racial groups. “Generalizability of ADNI results” (page unavailable) also documents differences in ancestry and education between ADNI and a community-based cohort. The copy does not establish that predictive signatures often underperform specifically in community cohorts because of differences in ancestry, education, and comorbid conditions. (LLM, conf=0.86)
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Roberts, K. F., Landsness, E. C., Reese, J., Elbert, D., Strobel, G., Wu, E., Chen, Y., Lai, A., Abrams, Z. B., Zhu, M., et al. (2026) · The Journal of Prevention of Alzheimer's Disease · doi:10.1016/j.tjpad.2025.100398 · Cited by 1 · see citing works
- Authors
- Veitch, D. P., Weiner, M. W., Miller, M., Aisen, P. S., Ashford, M. A., Beckett, L. A., Green, R. C., Harvey, D., Jack, C. R., Jagust, W., Landau, S. M., Morris, J. C., Nho, K. T., Nosheny, R., Okonkwo, O., Perrin, R. J., Petersen, R. C., Rivera Mindt, M., Saykin, A., Shaw, L. M., Toga, A. W., Tosun, D., & Initiative, F. T. A. D. N.
- Affiliations
- San Francisco VA Medical Center (US)
- University of Southern California (US)
- Department of Veterans Affairs Medical Center Northern California Institute for Research and Education (NCIRE) San Francisco California USA
- University of California, Davis (US)
- Broad Institute (US)
- Mayo Clinic (US)
- University of California, Berkeley (US)
- Washington University in St. Louis (US)
- Indiana University Indianapolis (US)
- University of Wisconsin–Madison (US)
- Department of Psychology Latin American and Latino Studies Institute African and African American Studies Fordham University New York New York USA
- University of Pennsylvania (US)
- Corresponding author
- Weiner, Michael W.
- ORCID
- Venue
- Alzheimer's & Dementia
- Publisher
- Wiley
- Published
- 2023-09-12
- Volume
- 20
- Issue
- 1
- Pages
- 652-694
- ISSN
- 1552-5260 (ISSN-L)
- 1552-5279
- PMC
- PMC10841343
- OpenAlex
- W4386624665
- Cited by
- 113
- References
- 18
- Citations by year
- 2026: 48 · 2025: 39 · 2024: 22 · 2023: 4
- FWCI
- 5.16
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Alzheimer s & Dementia (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- IUScholarWorks (Indiana University) (submittedVersion, cc-by-nc)
- Funders
- National Institutes of Health (U19 ‐AG 024904)
- National Institute on Aging
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- Alzheimer's disease, Alzheimer's Disease Neuroimaging Initiative
- MeSH terms
- Alzheimer Disease, Humans, Biomarkers, Amyloid beta-Peptides, tau Proteins, Disease Progression, Neuroimaging, Cognitive Dysfunction
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
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