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Corpus Callosum Radiomics-Based Classification Model in Alzheimer's Disease: A Case-Control Study
Background: Alzheimer's disease (AD) is a progressive neurodegenerative disease that causes the decline of some cognitive impairments. The present study aimed to identify the corpus callosum (CC) radiomic features related to the diagnosis of AD and build and evaluate a classification model. Met...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6070743/ https://www.ncbi.nlm.nih.gov/pubmed/30093881 http://dx.doi.org/10.3389/fneur.2018.00618 |
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author | Feng, Qi Chen, Yuanjun Liao, Zhengluan Jiang, Hongyang Mao, Dewang Wang, Mei Yu, Enyan Ding, Zhongxiang |
author_facet | Feng, Qi Chen, Yuanjun Liao, Zhengluan Jiang, Hongyang Mao, Dewang Wang, Mei Yu, Enyan Ding, Zhongxiang |
author_sort | Feng, Qi |
collection | PubMed |
description | Background: Alzheimer's disease (AD) is a progressive neurodegenerative disease that causes the decline of some cognitive impairments. The present study aimed to identify the corpus callosum (CC) radiomic features related to the diagnosis of AD and build and evaluate a classification model. Methods: Radiomics analysis was applied to the three-dimensional T1-weighted magnetization-prepared rapid gradient echo (MPRAGE) images of 78 patients with AD and 44 healthy controls (HC). The CC, in each subject, was segmented manually and 385 features were obtained after calculation. Then, the feature selection were carried out. The logistic regression model was constructed and evaluated according to identified features. Thus, the model can be used for distinguishing the AD from HC subjects. Results: Eleven features were selected from the three-dimensional T1-weighted MPRAGE images using the LASSO model, following which, the logistic regression model was constructed. The area under the receiver operating characteristic curve values (AUC), sensitivity, specificity, accuracy, precision, and positive and negative predictive values were 0.720, 0.792, 0.500, 0.684, 0.731, 0.731, and 0.583, respectively. Conclusion: The results demonstrated the potential of CC texture features as a biomarker for the diagnosis of AD. This is the first study showing that the radiomics model based on machine learning was a valuable method for the diagnosis of AD. |
format | Online Article Text |
id | pubmed-6070743 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60707432018-08-09 Corpus Callosum Radiomics-Based Classification Model in Alzheimer's Disease: A Case-Control Study Feng, Qi Chen, Yuanjun Liao, Zhengluan Jiang, Hongyang Mao, Dewang Wang, Mei Yu, Enyan Ding, Zhongxiang Front Neurol Neurology Background: Alzheimer's disease (AD) is a progressive neurodegenerative disease that causes the decline of some cognitive impairments. The present study aimed to identify the corpus callosum (CC) radiomic features related to the diagnosis of AD and build and evaluate a classification model. Methods: Radiomics analysis was applied to the three-dimensional T1-weighted magnetization-prepared rapid gradient echo (MPRAGE) images of 78 patients with AD and 44 healthy controls (HC). The CC, in each subject, was segmented manually and 385 features were obtained after calculation. Then, the feature selection were carried out. The logistic regression model was constructed and evaluated according to identified features. Thus, the model can be used for distinguishing the AD from HC subjects. Results: Eleven features were selected from the three-dimensional T1-weighted MPRAGE images using the LASSO model, following which, the logistic regression model was constructed. The area under the receiver operating characteristic curve values (AUC), sensitivity, specificity, accuracy, precision, and positive and negative predictive values were 0.720, 0.792, 0.500, 0.684, 0.731, 0.731, and 0.583, respectively. Conclusion: The results demonstrated the potential of CC texture features as a biomarker for the diagnosis of AD. This is the first study showing that the radiomics model based on machine learning was a valuable method for the diagnosis of AD. Frontiers Media S.A. 2018-07-26 /pmc/articles/PMC6070743/ /pubmed/30093881 http://dx.doi.org/10.3389/fneur.2018.00618 Text en Copyright © 2018 Feng, Chen, Liao, Jiang, Mao, Wang, Yu and Ding. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neurology Feng, Qi Chen, Yuanjun Liao, Zhengluan Jiang, Hongyang Mao, Dewang Wang, Mei Yu, Enyan Ding, Zhongxiang Corpus Callosum Radiomics-Based Classification Model in Alzheimer's Disease: A Case-Control Study |
title | Corpus Callosum Radiomics-Based Classification Model in Alzheimer's Disease: A Case-Control Study |
title_full | Corpus Callosum Radiomics-Based Classification Model in Alzheimer's Disease: A Case-Control Study |
title_fullStr | Corpus Callosum Radiomics-Based Classification Model in Alzheimer's Disease: A Case-Control Study |
title_full_unstemmed | Corpus Callosum Radiomics-Based Classification Model in Alzheimer's Disease: A Case-Control Study |
title_short | Corpus Callosum Radiomics-Based Classification Model in Alzheimer's Disease: A Case-Control Study |
title_sort | corpus callosum radiomics-based classification model in alzheimer's disease: a case-control study |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6070743/ https://www.ncbi.nlm.nih.gov/pubmed/30093881 http://dx.doi.org/10.3389/fneur.2018.00618 |
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