Cargando…
Dependency criterion based brain pathological age estimation of Alzheimer’s disease patients with MR scans
OBJECTIVES: Traditional brain age estimation methods are based on the idea that uses the real age as the training label. However, these methods ignore that there is a deviation between the real age and the brain age due to the accelerated brain aging. METHODS: This paper considers this deviation and...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5404315/ https://www.ncbi.nlm.nih.gov/pubmed/28438167 http://dx.doi.org/10.1186/s12938-017-0342-y |
_version_ | 1783231575319642112 |
---|---|
author | Li, Yongming Liu, Yuchuan Wang, Pin Wang, Jie Xu, Sha Qiu, Mingguo |
author_facet | Li, Yongming Liu, Yuchuan Wang, Pin Wang, Jie Xu, Sha Qiu, Mingguo |
author_sort | Li, Yongming |
collection | PubMed |
description | OBJECTIVES: Traditional brain age estimation methods are based on the idea that uses the real age as the training label. However, these methods ignore that there is a deviation between the real age and the brain age due to the accelerated brain aging. METHODS: This paper considers this deviation and obtains it by maximizing the correlation between the estimated brain age and the class label rather than by minimizing the difference between the estimated brain age and the real age. Firstly, set the search range of the deviation as the deviation candidates according to the prior knowledge. Secondly, use the support vector regression as the age estimation model to minimize the difference between the estimated age and the real age plus deviation rather than the real age itself. Thirdly, design the fitness function based on the correlation criterion. Fourthly, conduct age estimation on the validation dataset using the trained age estimation model, put the estimated age into the fitness function, and obtain the fitness value of the deviation candidate. Fifthly, repeat the iteration until all the deviation candidates are involved and get the optimal deviation with maximum fitness values. The real age plus the optimal deviation is taken as the brain pathological age. RESULTS: The experimental results showed that the separability of the samples was apparently improved. For normal control- Alzheimer’s disease (NC-AD), normal control- mild cognition impairment (NC-MCI), and mild cognition impairment—Alzheimer’s disease (MCI-AD), the average improvements were 0.164 (31.66%), 0.1284 (34.29%), and 0.0206 (7.1%), respectively. For NC-MCI-AD, the average improvement was 0.2002 (50.39%). The estimated brain pathological age could be not only more helpful for the classification of AD but also more precisely reflect the accelerated brain aging. CONCLUSION: In conclusion, this paper proposes a new kind of brain age—brain pathological age and offers an estimation method for it that can distinguish different states of AD, thereby better reflecting accelerated brain aging. Besides, the brain pathological age is most helpful for feature reduction, thereby simplifying the relevant classification algorithm. |
format | Online Article Text |
id | pubmed-5404315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-54043152017-04-27 Dependency criterion based brain pathological age estimation of Alzheimer’s disease patients with MR scans Li, Yongming Liu, Yuchuan Wang, Pin Wang, Jie Xu, Sha Qiu, Mingguo Biomed Eng Online Research OBJECTIVES: Traditional brain age estimation methods are based on the idea that uses the real age as the training label. However, these methods ignore that there is a deviation between the real age and the brain age due to the accelerated brain aging. METHODS: This paper considers this deviation and obtains it by maximizing the correlation between the estimated brain age and the class label rather than by minimizing the difference between the estimated brain age and the real age. Firstly, set the search range of the deviation as the deviation candidates according to the prior knowledge. Secondly, use the support vector regression as the age estimation model to minimize the difference between the estimated age and the real age plus deviation rather than the real age itself. Thirdly, design the fitness function based on the correlation criterion. Fourthly, conduct age estimation on the validation dataset using the trained age estimation model, put the estimated age into the fitness function, and obtain the fitness value of the deviation candidate. Fifthly, repeat the iteration until all the deviation candidates are involved and get the optimal deviation with maximum fitness values. The real age plus the optimal deviation is taken as the brain pathological age. RESULTS: The experimental results showed that the separability of the samples was apparently improved. For normal control- Alzheimer’s disease (NC-AD), normal control- mild cognition impairment (NC-MCI), and mild cognition impairment—Alzheimer’s disease (MCI-AD), the average improvements were 0.164 (31.66%), 0.1284 (34.29%), and 0.0206 (7.1%), respectively. For NC-MCI-AD, the average improvement was 0.2002 (50.39%). The estimated brain pathological age could be not only more helpful for the classification of AD but also more precisely reflect the accelerated brain aging. CONCLUSION: In conclusion, this paper proposes a new kind of brain age—brain pathological age and offers an estimation method for it that can distinguish different states of AD, thereby better reflecting accelerated brain aging. Besides, the brain pathological age is most helpful for feature reduction, thereby simplifying the relevant classification algorithm. BioMed Central 2017-04-24 /pmc/articles/PMC5404315/ /pubmed/28438167 http://dx.doi.org/10.1186/s12938-017-0342-y Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Li, Yongming Liu, Yuchuan Wang, Pin Wang, Jie Xu, Sha Qiu, Mingguo Dependency criterion based brain pathological age estimation of Alzheimer’s disease patients with MR scans |
title | Dependency criterion based brain pathological age estimation of Alzheimer’s disease patients with MR scans |
title_full | Dependency criterion based brain pathological age estimation of Alzheimer’s disease patients with MR scans |
title_fullStr | Dependency criterion based brain pathological age estimation of Alzheimer’s disease patients with MR scans |
title_full_unstemmed | Dependency criterion based brain pathological age estimation of Alzheimer’s disease patients with MR scans |
title_short | Dependency criterion based brain pathological age estimation of Alzheimer’s disease patients with MR scans |
title_sort | dependency criterion based brain pathological age estimation of alzheimer’s disease patients with mr scans |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5404315/ https://www.ncbi.nlm.nih.gov/pubmed/28438167 http://dx.doi.org/10.1186/s12938-017-0342-y |
work_keys_str_mv | AT liyongming dependencycriterionbasedbrainpathologicalageestimationofalzheimersdiseasepatientswithmrscans AT liuyuchuan dependencycriterionbasedbrainpathologicalageestimationofalzheimersdiseasepatientswithmrscans AT wangpin dependencycriterionbasedbrainpathologicalageestimationofalzheimersdiseasepatientswithmrscans AT wangjie dependencycriterionbasedbrainpathologicalageestimationofalzheimersdiseasepatientswithmrscans AT xusha dependencycriterionbasedbrainpathologicalageestimationofalzheimersdiseasepatientswithmrscans AT qiumingguo dependencycriterionbasedbrainpathologicalageestimationofalzheimersdiseasepatientswithmrscans AT dependencycriterionbasedbrainpathologicalageestimationofalzheimersdiseasepatientswithmrscans |