Cited by 190Dementia and Cognitive Impairment ResearchAlzheimer's disease research and treatmentsArtificial Intelligence in Healthcare

The DOI matches its Crossref record; 69 of the 74 references it cites were found in a registry or an index.

Boosting power for clinical trials using classifiers based on multiple biomarkers

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Abstract

Machine learning methods pool diverse information to perform computer-assisted diagnosis and predict future clinical decline. We introduce a machine learning method to boost power in clinical trials. We created a Support Vector Machine algorithm that combines brain imaging and other biomarkers to classify 737 Alzheimer's disease Neuroimaging initiative (ADNI) subjects as having Alzheimer's disease (AD), mild cognitive impairment (MCI), or normal controls. We trained our classifiers based on example data including: MRI measures of hippocampal, ventricular, and temporal lobe volumes, a PET-FDG numerical summary, CSF biomarkers (t-tau, p-tau, and Abeta(42)), ApoE genotype, age, sex, and body mass index. MRI measures contributed most to Alzheimer's disease (AD) classification; PET-FDG and CSF biomarkers, particularly Abeta(42), contributed more to MCI classification. Using all biomarkers jointly, we used our classifier to select the one-third of the subjects most likely to decline. In this subsample, fewer than 40 AD and MCI subjects would be needed to detect a 25% slowing in temporal lobe atrophy rates with 80% power--a substantial boosting of power relative to standard imaging measures.

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Crossref · 10.1016/j.neurobiolaging.2010.04.022

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Research works printed but not linked: 4

  1. 2009, Alzheimer's disease facts and figures, Alzheimers Dement, 5, 234, 10.1016/j.jalz.2009.03.001 · DOI
  2. Cummings, 2007, Disease-modifying therapies for Alzheimer disease: challenges to early intervention, Neurology, 69, 1622, 10.1212/01.wnl.0000295996.54210.69 · DOI
  3. Freund, 1999, Short introduction to boosting, J Jap Soc Artif Intell, 14, 771
  4. Zhang, 2008, Use of the Support Vector Machine and Sensitivity of an AD-Related Region-of-Interest Gray Matter Classifier in Identifying Amnestic MCI Subjects Who Convert t6o AD: Preliminary Findings From the AD Neuroimaging Initiative, Presented at the International Conference on Alzheimer's Disease, Chicago, July 26–, 31, 2008

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Metadata

Authors
Kohannim, O., Hua, X., Hibar, D. P., Lee, S., Chou, Y.-Y., Toga, A. W., Jack, C. R., Weiner, M. W., & Thompson, P. M.
Affiliations
  • University of California, Los Angeles (US)
  • Mayo Clinic (US)
  • University of California, San Francisco (US)
Corresponding author
Thompson, Paul M.
Venue
Neurobiology of Aging
Publisher
Elsevier BV
Published
2010-08
Volume
31
Issue
8
Pages
1429-1442
ISSN
0197-4580 (ISSN-L)
OpenAlex
W2167638846
Cited by
190
References
74
Citations by year
2026: 4 · 2025: 7 · 2024: 6 · 2023: 13 · 2022: 11 · 2021: 6 · 2020: 11 · 2019: 11 · 2018: 11 · 2017: 10 · 2016: 9 · 2015: 13 · 2014: 19 · 2013: 22 · 2012: 10
FWCI
12.31
Type
journal article
Language
en
Open access
Locations
  • Neurobiology of Aging (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • Alzheimer's Drug Discovery Foundation
  • Pfizer
  • Merck
  • University of Pennsylvania
  • F. Hoffmann-La Roche
  • Medpace
  • National Institutes of Health (5u01ag024904-10)
  • National Institute on Aging (U01-AG-024904, P30AG010129, K01AG030514, U19AG010483)
  • National Institute of Biomedical Imaging and Bioengineering
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
  • Health Sciences › Health Professions › Health Information Management › Artificial Intelligence in Healthcare
Keywords
Alzheimer's disease, mild cognitive impairment, support vector machine, combined biomarker detection, brain MRI, FDG-PET, cerebrospinal fluid biomarkers, amyloid-beta 42, APOE genotype, temporal lobe atrophy, computer-aided diagnosis, ADNI
MeSH terms
Age Factors, Aged, Aged, 80 and over, Alzheimer Disease, Artificial Intelligence, Cognition Disorders, Female, Genotype, Humans, Male, Sex Factors, Biomarkers, Randomized Controlled Trials as Topic, Apolipoprotein E4

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