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Predicting Progression to Clinical Alzheimer's Disease Dementia Using the Random Survival Forest
被引:3
|作者:
Song, Shangchen
[1
]
Asken, Breton
[2
,8
]
Armstrong, Melissa J.
[3
,4
,5
,7
]
Yang, Yang
[6
]
Li, Zhigang
[1
]
机构:
[1] Univ Florida, Coll Publ Hlth & Hlth Profess, Dept Biostat, Gainesville, FL USA
[2] Coll Med, Gainesville, FL USA
[3] Univ Florida, Dept Clin & Hlth Psychol, Coll Publ Hlth & Hlth Profess, Gainesville, FL USA
[4] Univ Florida, Coll Med, Dept Neurol, Gainesville, FL USA
[5] Univ Florida, Coll Med, Dept Hlth Outcomes & Biomed Informat, Gainesville, FL USA
[6] Univ Georgia, Franklin Coll Arts & Sci, Dept Stat, Athens, GA USA
[7] Univ Florida, Norman Fixel Inst Neurol Dis, Gainesville, FL USA
[8] Univ Florida, Ctr Cognit Aging & Memory, McKnight Brain Inst, Gainesville, FL USA
关键词:
Alzheimer's disease;
dementia;
machine learning;
survival analysis;
MODEL;
D O I:
10.3233/JAD-230208
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Background: Assessing the risk of developing clinical Alzheimer's disease (AD) dementia, by machine learning survival analysis approaches, among participants registered in Alzheimer's Disease Centers is important for AD dementia management. Objective: To construct a prediction model for the onset time of clinical AD dementia using the National Alzheimer Coordinating Center (NACC) and the Alzheimer's Disease Neuroimaging Initiative (ADNI) registered cohorts. Methods: A model was constructed using the Random Survival Forest (RSF) approach and internally and externally validated on the NACC cohort and the ADNI cohort. An R package and a Shiny app were provided for accessing the model. Results: We built a predictive model having the six predictors: delayed logical memory score (story recall), CDR (R) Dementia Staging Instrument - Sum of Boxes, general orientation in CDR (R), ability to remember dates and ability to pay bills in the Functional Activities Questionnaire, and patient age. The C indices of the model were 90.82% (SE = 0.71%) and 86.51% (SE = 0.75%) in NACC and ADNI respectively. The time-dependent AUC and accuracy at 48 months were 92.48% (SE = 1.12%) and 88.66% (SE = 1.00%) respectively in NACC, and 90.16% (SE = 1.12%) and 85.00% (SE = 1.14%) respectively in ADNI. Conclusion: The model showed good prediction performance and the six predictors were easy to obtain, cost-effective, and non-invasive. The model could be used to inform clinicians and patients on the probability of developing clinical AD dementia in 4 years with high accuracy.
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页码:535 / 548
页数:14
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