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Estimation of Human Cerebral Atrophy Based on Systemic Metabolic Status Using Machine Learning
BACKGROUND: Based on the assumption that systemic metabolic disorders affect cognitive function, we have developed a deep neural network (DNN) model that can estimate cognitive function based on basic blood test data that do not contain dementia-specific biomarkers. In this study, we used the same D...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9109818/ https://www.ncbi.nlm.nih.gov/pubmed/35585840 http://dx.doi.org/10.3389/fneur.2022.869915 |
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author | Sakatani, Kaoru Oyama, Katsunori Hu, Lizhen Warisawa, Shin'ichi |
author_facet | Sakatani, Kaoru Oyama, Katsunori Hu, Lizhen Warisawa, Shin'ichi |
author_sort | Sakatani, Kaoru |
collection | PubMed |
description | BACKGROUND: Based on the assumption that systemic metabolic disorders affect cognitive function, we have developed a deep neural network (DNN) model that can estimate cognitive function based on basic blood test data that do not contain dementia-specific biomarkers. In this study, we used the same DNN model to assess whether basic blood data can be used to estimate cerebral atrophy. METHODS: We used data from 1,310 subjects (58.32 ± 12.91years old) enrolled in the Brain Doc Bank. The average Mini Mental State Examination score was 28.6 ± 1.9. The degree of cerebral atrophy was determined using the MRI-based index (GM-BHQ). First, we evaluated the correlations between the subjects' age, blood data, and GM-BHQ. Next, we developed DNN models to assess the GM-BHQ: one used subjects' age and blood data, while the other used only blood data for input items. RESULTS: There was a negative correlation between age and GM-BHQ scores (r = -0.71). The subjects' age was positively correlated with blood urea nitrogen (BUN) (r = 0.40), alkaline phosphatase (ALP) (r = 0.22), glucose (GLU) (r = 0.22), and negative correlations with red blood cell counts (RBC) (r = −0.29) and platelet counts (PLT) (r = −0.26). GM-BHQ correlated with BUN (r = −0.30), GLU (r = −0.26), PLT (r = 0.26), and ALP (r = 0.22). The GM-BHQ estimated by the DNN model with subject age exhibited a positive correlation with the ground truth GM-BHQ (r = 0.70). Furthermore, even if the DNN model without subject age was used, the estimated GM-BHQ showed a significant positive correlation with ground truth GM-BHQ (r = 0.58). Age was the most important variable for estimating GM-BHQ. DISCUSSION: Aging had the greatest effect on cerebral atrophy. Aging also affects various organs, such as the kidney, and causes changes in systemic metabolic status, which may contribute to cerebral atrophy and cognitive impairment. The DNN model may serve as a new screening test for dementia using basic blood tests for health examinations. Finally, the blood data reflect systemic metabolic disorders in each subject—this method may thus contribute to personalized care. |
format | Online Article Text |
id | pubmed-9109818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91098182022-05-17 Estimation of Human Cerebral Atrophy Based on Systemic Metabolic Status Using Machine Learning Sakatani, Kaoru Oyama, Katsunori Hu, Lizhen Warisawa, Shin'ichi Front Neurol Neurology BACKGROUND: Based on the assumption that systemic metabolic disorders affect cognitive function, we have developed a deep neural network (DNN) model that can estimate cognitive function based on basic blood test data that do not contain dementia-specific biomarkers. In this study, we used the same DNN model to assess whether basic blood data can be used to estimate cerebral atrophy. METHODS: We used data from 1,310 subjects (58.32 ± 12.91years old) enrolled in the Brain Doc Bank. The average Mini Mental State Examination score was 28.6 ± 1.9. The degree of cerebral atrophy was determined using the MRI-based index (GM-BHQ). First, we evaluated the correlations between the subjects' age, blood data, and GM-BHQ. Next, we developed DNN models to assess the GM-BHQ: one used subjects' age and blood data, while the other used only blood data for input items. RESULTS: There was a negative correlation between age and GM-BHQ scores (r = -0.71). The subjects' age was positively correlated with blood urea nitrogen (BUN) (r = 0.40), alkaline phosphatase (ALP) (r = 0.22), glucose (GLU) (r = 0.22), and negative correlations with red blood cell counts (RBC) (r = −0.29) and platelet counts (PLT) (r = −0.26). GM-BHQ correlated with BUN (r = −0.30), GLU (r = −0.26), PLT (r = 0.26), and ALP (r = 0.22). The GM-BHQ estimated by the DNN model with subject age exhibited a positive correlation with the ground truth GM-BHQ (r = 0.70). Furthermore, even if the DNN model without subject age was used, the estimated GM-BHQ showed a significant positive correlation with ground truth GM-BHQ (r = 0.58). Age was the most important variable for estimating GM-BHQ. DISCUSSION: Aging had the greatest effect on cerebral atrophy. Aging also affects various organs, such as the kidney, and causes changes in systemic metabolic status, which may contribute to cerebral atrophy and cognitive impairment. The DNN model may serve as a new screening test for dementia using basic blood tests for health examinations. Finally, the blood data reflect systemic metabolic disorders in each subject—this method may thus contribute to personalized care. Frontiers Media S.A. 2022-05-02 /pmc/articles/PMC9109818/ /pubmed/35585840 http://dx.doi.org/10.3389/fneur.2022.869915 Text en Copyright © 2022 Sakatani, Oyama, Hu and Warisawa. https://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 Sakatani, Kaoru Oyama, Katsunori Hu, Lizhen Warisawa, Shin'ichi Estimation of Human Cerebral Atrophy Based on Systemic Metabolic Status Using Machine Learning |
title | Estimation of Human Cerebral Atrophy Based on Systemic Metabolic Status Using Machine Learning |
title_full | Estimation of Human Cerebral Atrophy Based on Systemic Metabolic Status Using Machine Learning |
title_fullStr | Estimation of Human Cerebral Atrophy Based on Systemic Metabolic Status Using Machine Learning |
title_full_unstemmed | Estimation of Human Cerebral Atrophy Based on Systemic Metabolic Status Using Machine Learning |
title_short | Estimation of Human Cerebral Atrophy Based on Systemic Metabolic Status Using Machine Learning |
title_sort | estimation of human cerebral atrophy based on systemic metabolic status using machine learning |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9109818/ https://www.ncbi.nlm.nih.gov/pubmed/35585840 http://dx.doi.org/10.3389/fneur.2022.869915 |
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