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Predicting conversion to Alzheimer's disease among individual high‐risk patients using the Characterizing AD Risk Events index model

AIMS: Both amnestic mild cognitive impairment (aMCI) and remitted late‐onset depression (rLOD) confer a high risk of developing Alzheimer's disease (AD). This study aims to determine whether the Characterizing AD Risk Events (CARE) index model can effectively predict conversion in individuals a...

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Autores principales: Lu, Xiang, Chen, Jiu, Shu, Hao, Wang, Zan, Shi, Yong‐mei, Yuan, Yong‐gui, Xie, Chun‐ming, Liao, Wen‐xiang, Su, Fan, Shi, Ya‐chen, Zhang, Zhi‐jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7298996/
https://www.ncbi.nlm.nih.gov/pubmed/32243064
http://dx.doi.org/10.1111/cns.13371
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author Lu, Xiang
Chen, Jiu
Shu, Hao
Wang, Zan
Shi, Yong‐mei
Yuan, Yong‐gui
Xie, Chun‐ming
Liao, Wen‐xiang
Su, Fan
Shi, Ya‐chen
Zhang, Zhi‐jun
author_facet Lu, Xiang
Chen, Jiu
Shu, Hao
Wang, Zan
Shi, Yong‐mei
Yuan, Yong‐gui
Xie, Chun‐ming
Liao, Wen‐xiang
Su, Fan
Shi, Ya‐chen
Zhang, Zhi‐jun
author_sort Lu, Xiang
collection PubMed
description AIMS: Both amnestic mild cognitive impairment (aMCI) and remitted late‐onset depression (rLOD) confer a high risk of developing Alzheimer's disease (AD). This study aims to determine whether the Characterizing AD Risk Events (CARE) index model can effectively predict conversion in individuals at high risk for AD development either in an independent aMCI population or in an rLOD population. METHODS: The CARE index model was constructed based on the event‐based probabilistic framework fusion of AD biomarkers to differentiate individuals progressing to AD from cognitively stable individuals in the aMCI population (27 stable subjects, 6 progressive subjects) and rLOD population (29 stable subjects, 10 progressive subjects) during the follow‐up period. RESULTS: AD diagnoses were predicted in the aMCI population with a balanced accuracy of 80.6%, a sensitivity of 83.3%, and a specificity of 77.8%. They were also predicted in the rLOD population with a balanced accuracy of 74.5%, a sensitivity of 80.0%, and a specificity of 69.0%. In addition, the CARE index scores were observed to be negatively correlated with the composite Z scores for episodic memory (R (2) = .17, P < .001) at baseline in the combined high‐risk population (N = 72). CONCLUSIONS: The CARE index model can be used for the prediction of conversion to AD in both aMCI and rLOD populations effectively. Additionally, it can be used to monitor the disease severity of patients.
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spelling pubmed-72989962020-06-18 Predicting conversion to Alzheimer's disease among individual high‐risk patients using the Characterizing AD Risk Events index model Lu, Xiang Chen, Jiu Shu, Hao Wang, Zan Shi, Yong‐mei Yuan, Yong‐gui Xie, Chun‐ming Liao, Wen‐xiang Su, Fan Shi, Ya‐chen Zhang, Zhi‐jun CNS Neurosci Ther Original Articles AIMS: Both amnestic mild cognitive impairment (aMCI) and remitted late‐onset depression (rLOD) confer a high risk of developing Alzheimer's disease (AD). This study aims to determine whether the Characterizing AD Risk Events (CARE) index model can effectively predict conversion in individuals at high risk for AD development either in an independent aMCI population or in an rLOD population. METHODS: The CARE index model was constructed based on the event‐based probabilistic framework fusion of AD biomarkers to differentiate individuals progressing to AD from cognitively stable individuals in the aMCI population (27 stable subjects, 6 progressive subjects) and rLOD population (29 stable subjects, 10 progressive subjects) during the follow‐up period. RESULTS: AD diagnoses were predicted in the aMCI population with a balanced accuracy of 80.6%, a sensitivity of 83.3%, and a specificity of 77.8%. They were also predicted in the rLOD population with a balanced accuracy of 74.5%, a sensitivity of 80.0%, and a specificity of 69.0%. In addition, the CARE index scores were observed to be negatively correlated with the composite Z scores for episodic memory (R (2) = .17, P < .001) at baseline in the combined high‐risk population (N = 72). CONCLUSIONS: The CARE index model can be used for the prediction of conversion to AD in both aMCI and rLOD populations effectively. Additionally, it can be used to monitor the disease severity of patients. John Wiley and Sons Inc. 2020-04-03 /pmc/articles/PMC7298996/ /pubmed/32243064 http://dx.doi.org/10.1111/cns.13371 Text en © 2020 The Authors. CNS Neuroscience & Therapeutics Published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Lu, Xiang
Chen, Jiu
Shu, Hao
Wang, Zan
Shi, Yong‐mei
Yuan, Yong‐gui
Xie, Chun‐ming
Liao, Wen‐xiang
Su, Fan
Shi, Ya‐chen
Zhang, Zhi‐jun
Predicting conversion to Alzheimer's disease among individual high‐risk patients using the Characterizing AD Risk Events index model
title Predicting conversion to Alzheimer's disease among individual high‐risk patients using the Characterizing AD Risk Events index model
title_full Predicting conversion to Alzheimer's disease among individual high‐risk patients using the Characterizing AD Risk Events index model
title_fullStr Predicting conversion to Alzheimer's disease among individual high‐risk patients using the Characterizing AD Risk Events index model
title_full_unstemmed Predicting conversion to Alzheimer's disease among individual high‐risk patients using the Characterizing AD Risk Events index model
title_short Predicting conversion to Alzheimer's disease among individual high‐risk patients using the Characterizing AD Risk Events index model
title_sort predicting conversion to alzheimer's disease among individual high‐risk patients using the characterizing ad risk events index model
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7298996/
https://www.ncbi.nlm.nih.gov/pubmed/32243064
http://dx.doi.org/10.1111/cns.13371
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