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Quantitative electroencephalographic changes and hippocampal atrophy in diabetic patients with mild cognitive impairment in Ismailia region
BACKGROUND: Cognitive decline could start or get worse among elderly patients with diabetes mellitus more than elderly without diabetes mellitus. So, those diabetic elderly patients have more risk to develop Alzheimer’s disease and vascular dementia. PATIENTS AND METHODS: This study included 48 elde...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5982437/ https://www.ncbi.nlm.nih.gov/pubmed/29899657 http://dx.doi.org/10.1186/s41983-018-0018-y |
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author | Abo hagar, Ahmed Ashour, Yossri Abd El-Razek, Reda Elsamahy, Mohamed Shehab, Osama |
author_facet | Abo hagar, Ahmed Ashour, Yossri Abd El-Razek, Reda Elsamahy, Mohamed Shehab, Osama |
author_sort | Abo hagar, Ahmed |
collection | PubMed |
description | BACKGROUND: Cognitive decline could start or get worse among elderly patients with diabetes mellitus more than elderly without diabetes mellitus. So, those diabetic elderly patients have more risk to develop Alzheimer’s disease and vascular dementia. PATIENTS AND METHODS: This study included 48 elderly, grouped into three equal groups. First group included patients with diabetes mellitus and cognitive impairment. Second group included patients with diabetes mellitus and no cognitive impairment. The last group included the controls. Evaluation through Mini Mental State Examination, MRI brain, and Quantitative Electroencephalography (QEEG) recording was done for every studied elderly. RESULTS: MRI finding revealed that hippocampal atrophy was significantly more prevalent among diabetic patients with mild cognitive impairment (MCI) (37.5%). The QEEG showed increase in the distribution of alpha 1 (low alpha) waves among control and diabetic patients without MCI groups, while there was an increase in the distribution of alpha 2 (high alpha) among diabetic patients with MCI. The QEEG results revealed increased alpha 2/alpha 1 ratio among patients with hippocampal atrophy. CONCLUSIONS: Type 2 DM was suggested to increase the risk of cognitive impairment. The cognitive impairment in patients with diabetes mellitus was associated with changes in hippocampal volume and QEEG changes. |
format | Online Article Text |
id | pubmed-5982437 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-59824372018-06-11 Quantitative electroencephalographic changes and hippocampal atrophy in diabetic patients with mild cognitive impairment in Ismailia region Abo hagar, Ahmed Ashour, Yossri Abd El-Razek, Reda Elsamahy, Mohamed Shehab, Osama Egypt J Neurol Psychiatr Neurosurg Research BACKGROUND: Cognitive decline could start or get worse among elderly patients with diabetes mellitus more than elderly without diabetes mellitus. So, those diabetic elderly patients have more risk to develop Alzheimer’s disease and vascular dementia. PATIENTS AND METHODS: This study included 48 elderly, grouped into three equal groups. First group included patients with diabetes mellitus and cognitive impairment. Second group included patients with diabetes mellitus and no cognitive impairment. The last group included the controls. Evaluation through Mini Mental State Examination, MRI brain, and Quantitative Electroencephalography (QEEG) recording was done for every studied elderly. RESULTS: MRI finding revealed that hippocampal atrophy was significantly more prevalent among diabetic patients with mild cognitive impairment (MCI) (37.5%). The QEEG showed increase in the distribution of alpha 1 (low alpha) waves among control and diabetic patients without MCI groups, while there was an increase in the distribution of alpha 2 (high alpha) among diabetic patients with MCI. The QEEG results revealed increased alpha 2/alpha 1 ratio among patients with hippocampal atrophy. CONCLUSIONS: Type 2 DM was suggested to increase the risk of cognitive impairment. The cognitive impairment in patients with diabetes mellitus was associated with changes in hippocampal volume and QEEG changes. Springer Berlin Heidelberg 2018-06-01 2018 /pmc/articles/PMC5982437/ /pubmed/29899657 http://dx.doi.org/10.1186/s41983-018-0018-y Text en © The Author(s) 2018 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. |
spellingShingle | Research Abo hagar, Ahmed Ashour, Yossri Abd El-Razek, Reda Elsamahy, Mohamed Shehab, Osama Quantitative electroencephalographic changes and hippocampal atrophy in diabetic patients with mild cognitive impairment in Ismailia region |
title | Quantitative electroencephalographic changes and hippocampal atrophy in diabetic patients with mild cognitive impairment in Ismailia region |
title_full | Quantitative electroencephalographic changes and hippocampal atrophy in diabetic patients with mild cognitive impairment in Ismailia region |
title_fullStr | Quantitative electroencephalographic changes and hippocampal atrophy in diabetic patients with mild cognitive impairment in Ismailia region |
title_full_unstemmed | Quantitative electroencephalographic changes and hippocampal atrophy in diabetic patients with mild cognitive impairment in Ismailia region |
title_short | Quantitative electroencephalographic changes and hippocampal atrophy in diabetic patients with mild cognitive impairment in Ismailia region |
title_sort | quantitative electroencephalographic changes and hippocampal atrophy in diabetic patients with mild cognitive impairment in ismailia region |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5982437/ https://www.ncbi.nlm.nih.gov/pubmed/29899657 http://dx.doi.org/10.1186/s41983-018-0018-y |
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