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Screening and predicting progression from high-risk mild cognitive impairment to Alzheimer’s disease

Individuals with mild cognitive impairment (MCI) are clinically heterogeneous, with different risks of progression to Alzheimer’s disease. Regular follow-up and examination may be time-consuming and costly, especially for MRI and PET. Therefore, it is necessary to identify a more precise MRI populat...

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Autores principales: Ge, Xiao-Yan, Cui, Kai, Liu, Long, Qin, Yao, Cui, Jing, Han, Hong-Juan, Luo, Yan-Hong, Yu, Hong-Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8413294/
https://www.ncbi.nlm.nih.gov/pubmed/34475445
http://dx.doi.org/10.1038/s41598-021-96914-3
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author Ge, Xiao-Yan
Cui, Kai
Liu, Long
Qin, Yao
Cui, Jing
Han, Hong-Juan
Luo, Yan-Hong
Yu, Hong-Mei
author_facet Ge, Xiao-Yan
Cui, Kai
Liu, Long
Qin, Yao
Cui, Jing
Han, Hong-Juan
Luo, Yan-Hong
Yu, Hong-Mei
author_sort Ge, Xiao-Yan
collection PubMed
description Individuals with mild cognitive impairment (MCI) are clinically heterogeneous, with different risks of progression to Alzheimer’s disease. Regular follow-up and examination may be time-consuming and costly, especially for MRI and PET. Therefore, it is necessary to identify a more precise MRI population. In this study, a two-stage screening frame was proposed for evaluating the predictive utility of additional MRI measurements among high-risk MCI subjects. In the first stage, the K-means cluster was performed for trajectory-template based on two clinical assessments. In the second stage, high-risk individuals were filtered out and imputed into prognosis models with varying strategies. As a result, the ADAS-13 was more sensitive for filtering out high-risk individuals among patients with MCI. The optimal model included a change rate of clinical assessments and three neuroimaging measurements and was significantly associated with a net reclassification improvement (NRI) of 0.246 (95% CI 0.021, 0.848) and integrated discrimination improvement (IDI) of 0.090 (95% CI − 0.062, 0.170). The ADAS-13 longitudinal models had the best discrimination performance (Optimism-corrected concordance index = 0.830), as validated by the bootstrap method. Considering the limited medical and financial resources, our findings recommend follow-up MRI examination 1 year after identification for high-risk individuals, while regular clinical assessments for low-risk individuals.
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spelling pubmed-84132942021-09-03 Screening and predicting progression from high-risk mild cognitive impairment to Alzheimer’s disease Ge, Xiao-Yan Cui, Kai Liu, Long Qin, Yao Cui, Jing Han, Hong-Juan Luo, Yan-Hong Yu, Hong-Mei Sci Rep Article Individuals with mild cognitive impairment (MCI) are clinically heterogeneous, with different risks of progression to Alzheimer’s disease. Regular follow-up and examination may be time-consuming and costly, especially for MRI and PET. Therefore, it is necessary to identify a more precise MRI population. In this study, a two-stage screening frame was proposed for evaluating the predictive utility of additional MRI measurements among high-risk MCI subjects. In the first stage, the K-means cluster was performed for trajectory-template based on two clinical assessments. In the second stage, high-risk individuals were filtered out and imputed into prognosis models with varying strategies. As a result, the ADAS-13 was more sensitive for filtering out high-risk individuals among patients with MCI. The optimal model included a change rate of clinical assessments and three neuroimaging measurements and was significantly associated with a net reclassification improvement (NRI) of 0.246 (95% CI 0.021, 0.848) and integrated discrimination improvement (IDI) of 0.090 (95% CI − 0.062, 0.170). The ADAS-13 longitudinal models had the best discrimination performance (Optimism-corrected concordance index = 0.830), as validated by the bootstrap method. Considering the limited medical and financial resources, our findings recommend follow-up MRI examination 1 year after identification for high-risk individuals, while regular clinical assessments for low-risk individuals. Nature Publishing Group UK 2021-09-02 /pmc/articles/PMC8413294/ /pubmed/34475445 http://dx.doi.org/10.1038/s41598-021-96914-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ge, Xiao-Yan
Cui, Kai
Liu, Long
Qin, Yao
Cui, Jing
Han, Hong-Juan
Luo, Yan-Hong
Yu, Hong-Mei
Screening and predicting progression from high-risk mild cognitive impairment to Alzheimer’s disease
title Screening and predicting progression from high-risk mild cognitive impairment to Alzheimer’s disease
title_full Screening and predicting progression from high-risk mild cognitive impairment to Alzheimer’s disease
title_fullStr Screening and predicting progression from high-risk mild cognitive impairment to Alzheimer’s disease
title_full_unstemmed Screening and predicting progression from high-risk mild cognitive impairment to Alzheimer’s disease
title_short Screening and predicting progression from high-risk mild cognitive impairment to Alzheimer’s disease
title_sort screening and predicting progression from high-risk mild cognitive impairment to alzheimer’s disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8413294/
https://www.ncbi.nlm.nih.gov/pubmed/34475445
http://dx.doi.org/10.1038/s41598-021-96914-3
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