4.7 Article

Predictive value of ATN biomarker profiles in estimating disease progression in Alzheimer's disease dementia

期刊

ALZHEIMERS & DEMENTIA
卷 17, 期 11, 页码 1855-1867

出版社

WILEY
DOI: 10.1002/alz.12491

关键词

Alzheimer's disease; amyloid; biomarker profile; machine learning; mild cognitive impairment; neurodegeneration; predictive analytics; tau

资金

  1. National Institute of Health [NIAK23AG063993, P01-AG003949, P41 EB015922, U01 AG024904, P01AG026572, P01AG055367, R56AG058854, RF1AG051710]
  2. Alzheimer's Association [2019-AACSF-641329]
  3. CureAlzheimer's Fund
  4. Leonard and Sylvia Marx Foundation

向作者/读者索取更多资源

The study evaluated the value of the ATN biomarker classification system in predicting conversion from MCI to dementia, with data-driven approaches showing better performance in this prediction. Both classifiers using clinical features and classifiers using ATN biomarkers performed equally well in predicting progression to dementia.
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.

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