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The relationship of the serum endocan level with the CHA(2)DS(2)-VASc score in patients with paroxysmal atrial fibrillation
BACKGROUND: In this study considering the relationship between serum endocan and CHA(2)DS(2)-VASc score, we assumed that endocan level could be a new biomarker for stroke risk in patients with paroxysmal atrial fibrillation (PAF). It was examined that endocan could be an alternative to determine the...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809070/ https://www.ncbi.nlm.nih.gov/pubmed/33443627 http://dx.doi.org/10.1186/s43044-021-00132-1 |
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author | Ceyhun, Gökhan |
author_facet | Ceyhun, Gökhan |
author_sort | Ceyhun, Gökhan |
collection | PubMed |
description | BACKGROUND: In this study considering the relationship between serum endocan and CHA(2)DS(2)-VASc score, we assumed that endocan level could be a new biomarker for stroke risk in patients with paroxysmal atrial fibrillation (PAF). It was examined that endocan could be an alternative to determine the risk of stroke and anticoagulation strategy in patients with PAF. The CHA(2)DS(2)-VASc scores were calculated for 192 patients with PAF, and their serum endocan levels were measured. The patients were divided into two groups as those with low to moderate (0-1) and those with high (≥ 2) CHA(2)DS(2)-VASc scores, and the endocan levels were compared between these two groups. RESULTS: The serum endocan level was significantly higher in the high CHA(2)DS(2)-VASc score group (p < 0.001). In the multivariate logistic regression analysis, endocan, C-reactive protein, and low-density lipoprotein were found to be independent determinants of the CHA(2)DS(2)-VASc score. The predictive value of endocan was analyzed using the ROC curve analysis, which revealed that endocan predicted a high stroke risk (CHA(2)DS(2)-VASc ≥ 2) at 82.5% sensitivity and 71.2% specificity at the cutoff value of 1.342. CONCLUSION: This study indicates that endocan is significantly associated with CHA(2)DS(2)-VASc score. We demonstrated that endocan could be a new biomarker for the prediction of a high stroke risk among patients diagnosed with PAF. |
format | Online Article Text |
id | pubmed-7809070 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-78090702021-01-19 The relationship of the serum endocan level with the CHA(2)DS(2)-VASc score in patients with paroxysmal atrial fibrillation Ceyhun, Gökhan Egypt Heart J Research BACKGROUND: In this study considering the relationship between serum endocan and CHA(2)DS(2)-VASc score, we assumed that endocan level could be a new biomarker for stroke risk in patients with paroxysmal atrial fibrillation (PAF). It was examined that endocan could be an alternative to determine the risk of stroke and anticoagulation strategy in patients with PAF. The CHA(2)DS(2)-VASc scores were calculated for 192 patients with PAF, and their serum endocan levels were measured. The patients were divided into two groups as those with low to moderate (0-1) and those with high (≥ 2) CHA(2)DS(2)-VASc scores, and the endocan levels were compared between these two groups. RESULTS: The serum endocan level was significantly higher in the high CHA(2)DS(2)-VASc score group (p < 0.001). In the multivariate logistic regression analysis, endocan, C-reactive protein, and low-density lipoprotein were found to be independent determinants of the CHA(2)DS(2)-VASc score. The predictive value of endocan was analyzed using the ROC curve analysis, which revealed that endocan predicted a high stroke risk (CHA(2)DS(2)-VASc ≥ 2) at 82.5% sensitivity and 71.2% specificity at the cutoff value of 1.342. CONCLUSION: This study indicates that endocan is significantly associated with CHA(2)DS(2)-VASc score. We demonstrated that endocan could be a new biomarker for the prediction of a high stroke risk among patients diagnosed with PAF. Springer Berlin Heidelberg 2021-01-14 /pmc/articles/PMC7809070/ /pubmed/33443627 http://dx.doi.org/10.1186/s43044-021-00132-1 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Ceyhun, Gökhan The relationship of the serum endocan level with the CHA(2)DS(2)-VASc score in patients with paroxysmal atrial fibrillation |
title | The relationship of the serum endocan level with the CHA(2)DS(2)-VASc score in patients with paroxysmal atrial fibrillation |
title_full | The relationship of the serum endocan level with the CHA(2)DS(2)-VASc score in patients with paroxysmal atrial fibrillation |
title_fullStr | The relationship of the serum endocan level with the CHA(2)DS(2)-VASc score in patients with paroxysmal atrial fibrillation |
title_full_unstemmed | The relationship of the serum endocan level with the CHA(2)DS(2)-VASc score in patients with paroxysmal atrial fibrillation |
title_short | The relationship of the serum endocan level with the CHA(2)DS(2)-VASc score in patients with paroxysmal atrial fibrillation |
title_sort | relationship of the serum endocan level with the cha(2)ds(2)-vasc score in patients with paroxysmal atrial fibrillation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809070/ https://www.ncbi.nlm.nih.gov/pubmed/33443627 http://dx.doi.org/10.1186/s43044-021-00132-1 |
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