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Diagnostic Value of Serum Biomarkers for Differentiating Central and Peripheral Causes of Acute Vertigo
Background: In patients presenting with acute vertigo or dizziness, distinguishing central from peripheral is a diagnostic challenge. This study investigated potential serum markers for differentiating central and peripheral vertigo in patients with acute-onset vertigo. Methods: This prospective cas...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7096380/ https://www.ncbi.nlm.nih.gov/pubmed/32266274 http://dx.doi.org/10.3389/fmed.2020.00084 |
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author | Sohn, Jong-Hee Kim, Chul-Ho Lee, Sang-Hwa Kim, Jong Ho Lee, Jae Jun |
author_facet | Sohn, Jong-Hee Kim, Chul-Ho Lee, Sang-Hwa Kim, Jong Ho Lee, Jae Jun |
author_sort | Sohn, Jong-Hee |
collection | PubMed |
description | Background: In patients presenting with acute vertigo or dizziness, distinguishing central from peripheral is a diagnostic challenge. This study investigated potential serum markers for differentiating central and peripheral vertigo in patients with acute-onset vertigo. Methods: This prospective case–control study recruited consecutive participants from the Emergency Department, including patients with acute-onset vertigo or dizziness within 12 h and control subjects. We used enzyme-linked immunosorbent assays to measure the serum S100β, NSE, BDNF, GFAP, and IL-6 levels during the acute period. Results: The 114 study subjects included 28 patients with central vertigo (CV), 49 patients with peripheral vertigo (PV), and 37 age- and sex-matched healthy controls. No differences were found in risk factor distribution among the three groups. In patients with CV, the serum NSE and S100β levels were significantly (p < 0.05) elevated compared with the control and PV groups. The ROC analysis gave an AUC of 0.843 (95% CI = 0.753–0.932) for NSE and 0.787 (95% CI = 0.687–0.886) for S100β for predicting CV. However, there were no significant differences in the serum GFAP and BDNF levels among the CV, PV, and control groups. Conclusions: Serum NSE and S100β levels are significantly higher in patients with CV, such as occurs with posterior circulation ischemic stroke or vertebrobasilar insufficiency. S100β and NSE may serve as serum biomarkers for differentiating between CV and PV in patients with acute-onset vertigo. |
format | Online Article Text |
id | pubmed-7096380 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70963802020-04-07 Diagnostic Value of Serum Biomarkers for Differentiating Central and Peripheral Causes of Acute Vertigo Sohn, Jong-Hee Kim, Chul-Ho Lee, Sang-Hwa Kim, Jong Ho Lee, Jae Jun Front Med (Lausanne) Medicine Background: In patients presenting with acute vertigo or dizziness, distinguishing central from peripheral is a diagnostic challenge. This study investigated potential serum markers for differentiating central and peripheral vertigo in patients with acute-onset vertigo. Methods: This prospective case–control study recruited consecutive participants from the Emergency Department, including patients with acute-onset vertigo or dizziness within 12 h and control subjects. We used enzyme-linked immunosorbent assays to measure the serum S100β, NSE, BDNF, GFAP, and IL-6 levels during the acute period. Results: The 114 study subjects included 28 patients with central vertigo (CV), 49 patients with peripheral vertigo (PV), and 37 age- and sex-matched healthy controls. No differences were found in risk factor distribution among the three groups. In patients with CV, the serum NSE and S100β levels were significantly (p < 0.05) elevated compared with the control and PV groups. The ROC analysis gave an AUC of 0.843 (95% CI = 0.753–0.932) for NSE and 0.787 (95% CI = 0.687–0.886) for S100β for predicting CV. However, there were no significant differences in the serum GFAP and BDNF levels among the CV, PV, and control groups. Conclusions: Serum NSE and S100β levels are significantly higher in patients with CV, such as occurs with posterior circulation ischemic stroke or vertebrobasilar insufficiency. S100β and NSE may serve as serum biomarkers for differentiating between CV and PV in patients with acute-onset vertigo. Frontiers Media S.A. 2020-03-19 /pmc/articles/PMC7096380/ /pubmed/32266274 http://dx.doi.org/10.3389/fmed.2020.00084 Text en Copyright © 2020 Sohn, Kim, Lee, Kim and Lee. http://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 | Medicine Sohn, Jong-Hee Kim, Chul-Ho Lee, Sang-Hwa Kim, Jong Ho Lee, Jae Jun Diagnostic Value of Serum Biomarkers for Differentiating Central and Peripheral Causes of Acute Vertigo |
title | Diagnostic Value of Serum Biomarkers for Differentiating Central and Peripheral Causes of Acute Vertigo |
title_full | Diagnostic Value of Serum Biomarkers for Differentiating Central and Peripheral Causes of Acute Vertigo |
title_fullStr | Diagnostic Value of Serum Biomarkers for Differentiating Central and Peripheral Causes of Acute Vertigo |
title_full_unstemmed | Diagnostic Value of Serum Biomarkers for Differentiating Central and Peripheral Causes of Acute Vertigo |
title_short | Diagnostic Value of Serum Biomarkers for Differentiating Central and Peripheral Causes of Acute Vertigo |
title_sort | diagnostic value of serum biomarkers for differentiating central and peripheral causes of acute vertigo |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7096380/ https://www.ncbi.nlm.nih.gov/pubmed/32266274 http://dx.doi.org/10.3389/fmed.2020.00084 |
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