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Research on nonstroke dementia screening and cognitive function prediction model for older people based on brain atrophy characteristics
BACKGROUND: Brain atrophy is an important feature in dementia and is meaningful to explore a brain atrophy model to predict dementia. Using machine learning algorithm to establish a dementia model and cognitive function model based on brain atrophy characteristics is unstoppable. METHOD: We acquired...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9660432/ https://www.ncbi.nlm.nih.gov/pubmed/36278400 http://dx.doi.org/10.1002/brb3.2726 |
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author | Zhang, Wei Zheng, Xiaoran Li, Renren Liu, Meng Xiao, Weixin Huang, Lihe Xu, Feiyang Dong, Ningxin Li, Yunxia |
author_facet | Zhang, Wei Zheng, Xiaoran Li, Renren Liu, Meng Xiao, Weixin Huang, Lihe Xu, Feiyang Dong, Ningxin Li, Yunxia |
author_sort | Zhang, Wei |
collection | PubMed |
description | BACKGROUND: Brain atrophy is an important feature in dementia and is meaningful to explore a brain atrophy model to predict dementia. Using machine learning algorithm to establish a dementia model and cognitive function model based on brain atrophy characteristics is unstoppable. METHOD: We acquired 157 dementia and 156 normal old people.s clinical information and MRI data, which contains 44 brain atrophy features, including visual scale assessment of brain atrophy and multiple linear measurement indexes and brain atrophy index. Five machine learning models were used to establish prediction models for dementia, general cognition, and subcognitive domains. RESULTS: The extreme Gradient Boosting (XGBoost) model had the best effect in predicting dementia, with a sensitivity of 0.645, a specificity of 0.839, and the area under curve (AUC) of 0.784. In this model, the important brain atrophy features for predicting dementia were temporal horn ratio, cella media index, suprasellar cistern ratio, and the thickness of the corpus callosum genu. CONCLUSION: For nonstroke elderly people, the machine learning model based on clinical head MRI brain atrophy features had good predictive value for dementia, general cognitive impairment, immediate memory impairment, word fluency disorder, executive dysfunction, and visualspatial disorder. |
format | Online Article Text |
id | pubmed-9660432 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96604322022-11-14 Research on nonstroke dementia screening and cognitive function prediction model for older people based on brain atrophy characteristics Zhang, Wei Zheng, Xiaoran Li, Renren Liu, Meng Xiao, Weixin Huang, Lihe Xu, Feiyang Dong, Ningxin Li, Yunxia Brain Behav Original Articles BACKGROUND: Brain atrophy is an important feature in dementia and is meaningful to explore a brain atrophy model to predict dementia. Using machine learning algorithm to establish a dementia model and cognitive function model based on brain atrophy characteristics is unstoppable. METHOD: We acquired 157 dementia and 156 normal old people.s clinical information and MRI data, which contains 44 brain atrophy features, including visual scale assessment of brain atrophy and multiple linear measurement indexes and brain atrophy index. Five machine learning models were used to establish prediction models for dementia, general cognition, and subcognitive domains. RESULTS: The extreme Gradient Boosting (XGBoost) model had the best effect in predicting dementia, with a sensitivity of 0.645, a specificity of 0.839, and the area under curve (AUC) of 0.784. In this model, the important brain atrophy features for predicting dementia were temporal horn ratio, cella media index, suprasellar cistern ratio, and the thickness of the corpus callosum genu. CONCLUSION: For nonstroke elderly people, the machine learning model based on clinical head MRI brain atrophy features had good predictive value for dementia, general cognitive impairment, immediate memory impairment, word fluency disorder, executive dysfunction, and visualspatial disorder. John Wiley and Sons Inc. 2022-10-24 /pmc/articles/PMC9660432/ /pubmed/36278400 http://dx.doi.org/10.1002/brb3.2726 Text en © 2022 The Authors. Brain and Behavior published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://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 Zhang, Wei Zheng, Xiaoran Li, Renren Liu, Meng Xiao, Weixin Huang, Lihe Xu, Feiyang Dong, Ningxin Li, Yunxia Research on nonstroke dementia screening and cognitive function prediction model for older people based on brain atrophy characteristics |
title | Research on nonstroke dementia screening and cognitive function prediction model for older people based on brain atrophy characteristics |
title_full | Research on nonstroke dementia screening and cognitive function prediction model for older people based on brain atrophy characteristics |
title_fullStr | Research on nonstroke dementia screening and cognitive function prediction model for older people based on brain atrophy characteristics |
title_full_unstemmed | Research on nonstroke dementia screening and cognitive function prediction model for older people based on brain atrophy characteristics |
title_short | Research on nonstroke dementia screening and cognitive function prediction model for older people based on brain atrophy characteristics |
title_sort | research on nonstroke dementia screening and cognitive function prediction model for older people based on brain atrophy characteristics |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9660432/ https://www.ncbi.nlm.nih.gov/pubmed/36278400 http://dx.doi.org/10.1002/brb3.2726 |
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