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The Association Between Inflammatory Biomarkers and Vitamin D Level With the Evolution and Severity of Stroke
INTRODUCTION: Vitamin D deficiency has been linked to the evolution of ischemic stroke, but the data regarding the association between stroke severity and vitamin D level is scarce. METHODS: Patients with first-ever ischemic stroke in the middle cerebral artery territory, within seven days after the...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Tehran University of Medical Sciences
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10262286/ https://www.ncbi.nlm.nih.gov/pubmed/37323962 http://dx.doi.org/10.32598/bcn.2021.1971.1 |
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author | Safari, Anahid Fadakar, Nima Borhani-Haghighi, Afshin |
author_facet | Safari, Anahid Fadakar, Nima Borhani-Haghighi, Afshin |
author_sort | Safari, Anahid |
collection | PubMed |
description | INTRODUCTION: Vitamin D deficiency has been linked to the evolution of ischemic stroke, but the data regarding the association between stroke severity and vitamin D level is scarce. METHODS: Patients with first-ever ischemic stroke in the middle cerebral artery territory, within seven days after the stroke, were recruited. The control group included age- and gender-matched individuals. We compared 25-OH vitamin D (vitamin D), high sensitive C-reactive protein (hsCRP), serum amyloid A (SAA), and osteopontin levels between stroke patients and the control group. The association between stroke severity according to the National Institutes of Health Stroke Scale (NIHSS) and the Alberta stroke program early CT score (ASPECTS) and levels of vitamin D and inflammatory biomarkers were also studied. RESULTS: There was an association between hypertension (P=0.035), diabetes mellitus (P=0.043), smoking (P=0.016), history of ischemic heart disease (P=0.002), higher SAA (P<0.001), higher hsCRP (P<0.001), and lower vitamin D levels (P=0.002) and stroke evolution in a case-control study. Meanwhile, in stroke patients, its severity was associated with higher SAA (P=0.04) and hsCRP (P=0.001), and lower vitamin D levels (P=0.043) according to clinical scale (higher admission NIHSS). According to the ASPECT score, higher SAA (P=0.017) and hsCRP (P=0.007), but not lower vitamin D levels, were associated with more infarct areas (P=0.149). CONCLUSION: Vitamin D may play a role in both the evolution and severity of stroke. |
format | Online Article Text |
id | pubmed-10262286 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Tehran University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-102622862023-06-15 The Association Between Inflammatory Biomarkers and Vitamin D Level With the Evolution and Severity of Stroke Safari, Anahid Fadakar, Nima Borhani-Haghighi, Afshin Basic Clin Neurosci Research Paper INTRODUCTION: Vitamin D deficiency has been linked to the evolution of ischemic stroke, but the data regarding the association between stroke severity and vitamin D level is scarce. METHODS: Patients with first-ever ischemic stroke in the middle cerebral artery territory, within seven days after the stroke, were recruited. The control group included age- and gender-matched individuals. We compared 25-OH vitamin D (vitamin D), high sensitive C-reactive protein (hsCRP), serum amyloid A (SAA), and osteopontin levels between stroke patients and the control group. The association between stroke severity according to the National Institutes of Health Stroke Scale (NIHSS) and the Alberta stroke program early CT score (ASPECTS) and levels of vitamin D and inflammatory biomarkers were also studied. RESULTS: There was an association between hypertension (P=0.035), diabetes mellitus (P=0.043), smoking (P=0.016), history of ischemic heart disease (P=0.002), higher SAA (P<0.001), higher hsCRP (P<0.001), and lower vitamin D levels (P=0.002) and stroke evolution in a case-control study. Meanwhile, in stroke patients, its severity was associated with higher SAA (P=0.04) and hsCRP (P=0.001), and lower vitamin D levels (P=0.043) according to clinical scale (higher admission NIHSS). According to the ASPECT score, higher SAA (P=0.017) and hsCRP (P=0.007), but not lower vitamin D levels, were associated with more infarct areas (P=0.149). CONCLUSION: Vitamin D may play a role in both the evolution and severity of stroke. Tehran University of Medical Sciences 2022 2022-11-01 /pmc/articles/PMC10262286/ /pubmed/37323962 http://dx.doi.org/10.32598/bcn.2021.1971.1 Text en Copyright© 2022 Iranian Neuroscience Society https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) |
spellingShingle | Research Paper Safari, Anahid Fadakar, Nima Borhani-Haghighi, Afshin The Association Between Inflammatory Biomarkers and Vitamin D Level With the Evolution and Severity of Stroke |
title | The Association Between Inflammatory Biomarkers and Vitamin D Level With the Evolution and Severity of Stroke |
title_full | The Association Between Inflammatory Biomarkers and Vitamin D Level With the Evolution and Severity of Stroke |
title_fullStr | The Association Between Inflammatory Biomarkers and Vitamin D Level With the Evolution and Severity of Stroke |
title_full_unstemmed | The Association Between Inflammatory Biomarkers and Vitamin D Level With the Evolution and Severity of Stroke |
title_short | The Association Between Inflammatory Biomarkers and Vitamin D Level With the Evolution and Severity of Stroke |
title_sort | association between inflammatory biomarkers and vitamin d level with the evolution and severity of stroke |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10262286/ https://www.ncbi.nlm.nih.gov/pubmed/37323962 http://dx.doi.org/10.32598/bcn.2021.1971.1 |
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