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The importance of Vitamin-D and Neutrophil-Lymphocyte Ratio for Alzheimer’s Disease

OBJECTIVE: Ischemia and inflammation play a role in the pathophysiology of Alzheimer’s disease (AD). Plasma neutrophil–lymphocyte ratio (NLR), and 25- hydroxyvitamin D (vitamin D) were used as a biomarker for inflammation and atherosclerosis. The present study aimed to investigate a link between NLR...

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Autores principales: Evlice, Ahmet, Sanli, Zeynep Selcan, Boz, Pinar Bengi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Professional Medical Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10214823/
https://www.ncbi.nlm.nih.gov/pubmed/37250565
http://dx.doi.org/10.12669/pjms.39.3.7024
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author Evlice, Ahmet
Sanli, Zeynep Selcan
Boz, Pinar Bengi
author_facet Evlice, Ahmet
Sanli, Zeynep Selcan
Boz, Pinar Bengi
author_sort Evlice, Ahmet
collection PubMed
description OBJECTIVE: Ischemia and inflammation play a role in the pathophysiology of Alzheimer’s disease (AD). Plasma neutrophil–lymphocyte ratio (NLR), and 25- hydroxyvitamin D (vitamin D) were used as a biomarker for inflammation and atherosclerosis. The present study aimed to investigate a link between NLR, vitamin D and ischemia in AD. METHODS: The subjects with AD and control groups were enrolled to this retrospective study between 2017-2022 at Cukurova University Hospital. The cognitive assessment (MMSE), and blood tests (NLR, vitamin D) were collected from all subjects. In first part of the study, AD (n:132) and the control group (n:38) were compared. In second part of the study, magnetic resonance imaging (MRI) was used for evaluating ischemic lesions with scoring method of Fazekas. The control group (n:38) and AD subjects with mild ischemic lesions (Fazekas-1 and Fazekas-2) (n:64) were excluded. AD subjects with severe ischemic lesions (Fazekas-3) (n:34) and without ischemic lesions (Fazekas-0) (n:34) were compared again. SPSS 20.0 was used for all analyses. The threshold for statistical significance was set at 0.05. RESULTS: In the first part of the study, 132 AD patients (69 female and 63 male; mean age 70.83±9.35 (49-87) and age-matched 38 controls were compared. The mean NLR in AD [2.96±2.46 (1.17-19.43)] was higher than the control group [1.9±0.66 (0.9-3.56)] (p=0.005). In the second part of the study, the mean Vitamin D of Fazekas-3 AD group [16.15±9.64 (4.7-35)] was lower than Fazekas-0 AD group [16.27±6.81(4.6-29.7)] (p=0.024). CONCLUSION: NLR was higher in AD while there was no difference between the Fazekas-0 and Fazekas-3 AD groups. Vitamin D was lower in the Fazekas-3 AD group. These data suggested that NLR increased independently of ischemia in AD. Also vitamin D deficiency could trigger ischemia in AD.
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spelling pubmed-102148232023-05-27 The importance of Vitamin-D and Neutrophil-Lymphocyte Ratio for Alzheimer’s Disease Evlice, Ahmet Sanli, Zeynep Selcan Boz, Pinar Bengi Pak J Med Sci Original Article OBJECTIVE: Ischemia and inflammation play a role in the pathophysiology of Alzheimer’s disease (AD). Plasma neutrophil–lymphocyte ratio (NLR), and 25- hydroxyvitamin D (vitamin D) were used as a biomarker for inflammation and atherosclerosis. The present study aimed to investigate a link between NLR, vitamin D and ischemia in AD. METHODS: The subjects with AD and control groups were enrolled to this retrospective study between 2017-2022 at Cukurova University Hospital. The cognitive assessment (MMSE), and blood tests (NLR, vitamin D) were collected from all subjects. In first part of the study, AD (n:132) and the control group (n:38) were compared. In second part of the study, magnetic resonance imaging (MRI) was used for evaluating ischemic lesions with scoring method of Fazekas. The control group (n:38) and AD subjects with mild ischemic lesions (Fazekas-1 and Fazekas-2) (n:64) were excluded. AD subjects with severe ischemic lesions (Fazekas-3) (n:34) and without ischemic lesions (Fazekas-0) (n:34) were compared again. SPSS 20.0 was used for all analyses. The threshold for statistical significance was set at 0.05. RESULTS: In the first part of the study, 132 AD patients (69 female and 63 male; mean age 70.83±9.35 (49-87) and age-matched 38 controls were compared. The mean NLR in AD [2.96±2.46 (1.17-19.43)] was higher than the control group [1.9±0.66 (0.9-3.56)] (p=0.005). In the second part of the study, the mean Vitamin D of Fazekas-3 AD group [16.15±9.64 (4.7-35)] was lower than Fazekas-0 AD group [16.27±6.81(4.6-29.7)] (p=0.024). CONCLUSION: NLR was higher in AD while there was no difference between the Fazekas-0 and Fazekas-3 AD groups. Vitamin D was lower in the Fazekas-3 AD group. These data suggested that NLR increased independently of ischemia in AD. Also vitamin D deficiency could trigger ischemia in AD. Professional Medical Publications 2023 /pmc/articles/PMC10214823/ /pubmed/37250565 http://dx.doi.org/10.12669/pjms.39.3.7024 Text en Copyright: © Pakistan Journal of Medical Sciences https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0 (https://creativecommons.org/licenses/by/3.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Evlice, Ahmet
Sanli, Zeynep Selcan
Boz, Pinar Bengi
The importance of Vitamin-D and Neutrophil-Lymphocyte Ratio for Alzheimer’s Disease
title The importance of Vitamin-D and Neutrophil-Lymphocyte Ratio for Alzheimer’s Disease
title_full The importance of Vitamin-D and Neutrophil-Lymphocyte Ratio for Alzheimer’s Disease
title_fullStr The importance of Vitamin-D and Neutrophil-Lymphocyte Ratio for Alzheimer’s Disease
title_full_unstemmed The importance of Vitamin-D and Neutrophil-Lymphocyte Ratio for Alzheimer’s Disease
title_short The importance of Vitamin-D and Neutrophil-Lymphocyte Ratio for Alzheimer’s Disease
title_sort importance of vitamin-d and neutrophil-lymphocyte ratio for alzheimer’s disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10214823/
https://www.ncbi.nlm.nih.gov/pubmed/37250565
http://dx.doi.org/10.12669/pjms.39.3.7024
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