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Gray matter alterations and correlation of nutritional intake with the gray matter volume in prediabetes
The neurophysiology of prediabetes plays an important role in preventive medicine. The dysregulation of glucose metabolism is likely linked to changes in neuron-related gray matter. Therefore, we designed this study to investigate gray matter alterations in medication-naive prediabetic patients. We...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4998331/ https://www.ncbi.nlm.nih.gov/pubmed/27336893 http://dx.doi.org/10.1097/MD.0000000000003956 |
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author | Hou, Yi-Cheng Lai, Chien-Han Wu, Yu-Te Yang, Shwu-Huey |
author_facet | Hou, Yi-Cheng Lai, Chien-Han Wu, Yu-Te Yang, Shwu-Huey |
author_sort | Hou, Yi-Cheng |
collection | PubMed |
description | The neurophysiology of prediabetes plays an important role in preventive medicine. The dysregulation of glucose metabolism is likely linked to changes in neuron-related gray matter. Therefore, we designed this study to investigate gray matter alterations in medication-naive prediabetic patients. We expected to find alterations in the gray matter of prediabetic patients. A total of 64 prediabetic patients and 54 controls were enrolled. All subjects received T1 scans using a 3-T magnetic resonance imaging machine. Subjects also completed nutritional intake records at the 24-hour and 3-day time points to determine their carbohydrate, protein, fat, and total calorie intake. We utilized optimized voxel-based morphometry to estimate the gray matter differences between the patients and controls. In addition, the preprandial serum glucose level and the carbohydrate, protein, fat, and total calorie intake levels were tested to determine whether these parameters were correlated with the gray matter volume. Prediabetic patients had lower gray matter volumes than controls in the right anterior cingulate gyrus, right posterior cingulate gyrus, left insula, left super temporal gyrus, and left middle temporal gyrus (corrected P < 0.05; voxel threshold: 33). Gray matter volume in the right anterior cingulate was also negatively correlated with the preprandial serum glucose level gyrus in a voxel-dependent manner (r = –0.501; 2-tailed P = 0.001). The cingulo-temporal and insula gray matter alterations may be associated with the glucose dysregulation in prediabetic patients. |
format | Online Article Text |
id | pubmed-4998331 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-49983312016-09-02 Gray matter alterations and correlation of nutritional intake with the gray matter volume in prediabetes Hou, Yi-Cheng Lai, Chien-Han Wu, Yu-Te Yang, Shwu-Huey Medicine (Baltimore) 6800 The neurophysiology of prediabetes plays an important role in preventive medicine. The dysregulation of glucose metabolism is likely linked to changes in neuron-related gray matter. Therefore, we designed this study to investigate gray matter alterations in medication-naive prediabetic patients. We expected to find alterations in the gray matter of prediabetic patients. A total of 64 prediabetic patients and 54 controls were enrolled. All subjects received T1 scans using a 3-T magnetic resonance imaging machine. Subjects also completed nutritional intake records at the 24-hour and 3-day time points to determine their carbohydrate, protein, fat, and total calorie intake. We utilized optimized voxel-based morphometry to estimate the gray matter differences between the patients and controls. In addition, the preprandial serum glucose level and the carbohydrate, protein, fat, and total calorie intake levels were tested to determine whether these parameters were correlated with the gray matter volume. Prediabetic patients had lower gray matter volumes than controls in the right anterior cingulate gyrus, right posterior cingulate gyrus, left insula, left super temporal gyrus, and left middle temporal gyrus (corrected P < 0.05; voxel threshold: 33). Gray matter volume in the right anterior cingulate was also negatively correlated with the preprandial serum glucose level gyrus in a voxel-dependent manner (r = –0.501; 2-tailed P = 0.001). The cingulo-temporal and insula gray matter alterations may be associated with the glucose dysregulation in prediabetic patients. Wolters Kluwer Health 2016-06-24 /pmc/articles/PMC4998331/ /pubmed/27336893 http://dx.doi.org/10.1097/MD.0000000000003956 Text en Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0, where it is permissible to download, share and reproduce the work in any medium, provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by-nc-nd/4.0 |
spellingShingle | 6800 Hou, Yi-Cheng Lai, Chien-Han Wu, Yu-Te Yang, Shwu-Huey Gray matter alterations and correlation of nutritional intake with the gray matter volume in prediabetes |
title | Gray matter alterations and correlation of nutritional intake with the gray matter volume in prediabetes |
title_full | Gray matter alterations and correlation of nutritional intake with the gray matter volume in prediabetes |
title_fullStr | Gray matter alterations and correlation of nutritional intake with the gray matter volume in prediabetes |
title_full_unstemmed | Gray matter alterations and correlation of nutritional intake with the gray matter volume in prediabetes |
title_short | Gray matter alterations and correlation of nutritional intake with the gray matter volume in prediabetes |
title_sort | gray matter alterations and correlation of nutritional intake with the gray matter volume in prediabetes |
topic | 6800 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4998331/ https://www.ncbi.nlm.nih.gov/pubmed/27336893 http://dx.doi.org/10.1097/MD.0000000000003956 |
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