AD risk score for the early phases of disease based on unsupervised machine learning

Introduction Identifying cognitively normal individuals at high risk for progression to symptomatic Alzheimer's disease (AD) is critical for early intervention. Methods An AD risk score was derived using unsupervised machine learning. The score was developed using data from 226 cognitively norm...

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Published inAlzheimer's & dementia Vol. 16; no. 11; pp. 1524 - 1533
Main Authors Wang, Zheyu, Tang, Zhuojun, Zhu, Yuxin, Pettigrew, Corinne, Soldan, Anja, Gross, Alden, Albert, Marilyn
Format Journal Article
LanguageEnglish
Published United States 01.11.2020
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Summary:Introduction Identifying cognitively normal individuals at high risk for progression to symptomatic Alzheimer's disease (AD) is critical for early intervention. Methods An AD risk score was derived using unsupervised machine learning. The score was developed using data from 226 cognitively normal individuals and included cerebrospinal fluid, magnetic resonance imaging, and cognitive measures, and validated in an independent cohort. Results Higher baseline AD progression risk scores (hazard ratio = 2.70, P < 0.001) were associated with greater risks of progression to clinical symptoms of mild cognitive impairment (MCI). Baseline scores had an area under the curve of 0.83 (95% confidence interval: 0.75 to 0.91) for identifying subjects who progressed to MCI/dementia within 5 years. The validation procedure, using data from the Alzheimer's Disease Neuroimaging Initiative, demonstrated accuracy of prediction across the AD spectrum. Discussion The derived risk score provides high predictive accuracy for identifying which individuals with normal cognition are likely to show clinical decline due to AD within 5 years.
Bibliography:Data used in preparation of this article were obtained from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database (adni.loni.usc.edu). As such, the investigators within the ADNI contributed to the design and implementation of ADNI and/or provided data but did not participate in analysis or writing of this report. A complete listing of ADNI investigators can be found at
http://adni.loni.usc.edu/wp-content/uploads/how_to_apply/ADNI_Acknowledgement_List.pdf
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ISSN:1552-5260
1552-5279
1552-5279
DOI:10.1002/alz.12140