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Serum neuron-specific enolase, a marker of neuronal injury, increases after catheter ablation of atrial fibrillation
OBJECTIVE: Catheter ablation of atrial fibrillation (AF) can lead to thromboembolic complications, especially stroke. We measured the periprocedural serum neuron-specific enolase (NSE) level, which is a biomarker of neuronal injury, after ablation of AF. METHODS: Forty-three patients with paroxysmal...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259406/ https://www.ncbi.nlm.nih.gov/pubmed/30185093 http://dx.doi.org/10.1177/0300060518767768 |
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author | Acibuca, Aynur Vurgun, Veysel Kutay Gerede, Demet Menekse Altin, Ali Timucin Gul, Inci Sule Candemir, Basar Isikay Togay, Canan Kilickap, Mustafa Akyurek, Omer |
author_facet | Acibuca, Aynur Vurgun, Veysel Kutay Gerede, Demet Menekse Altin, Ali Timucin Gul, Inci Sule Candemir, Basar Isikay Togay, Canan Kilickap, Mustafa Akyurek, Omer |
author_sort | Acibuca, Aynur |
collection | PubMed |
description | OBJECTIVE: Catheter ablation of atrial fibrillation (AF) can lead to thromboembolic complications, especially stroke. We measured the periprocedural serum neuron-specific enolase (NSE) level, which is a biomarker of neuronal injury, after ablation of AF. METHODS: Forty-three patients with paroxysmal AF were prospectively enrolled before radiofrequency ablation. A neurological examination was performed before and after the procedure. The serum NSE level was determined before and at the end of the procedure and at 2, 24, and 48 h after the procedure. RESULTS: No patients developed new neurological deficits. However, the median (interquartile range) NSE level increased after ablation from 6.7 (3.87) ng/mL at baseline to 11.48 (5.3) ng/mL at 24 h postoperatively. The NSE level exceed the upper reference limit of normal (17 ng/mL) in 14 patients (33%), and these patients were found to have a larger left atrium. CONCLUSIONS: Serum NSE increased in most of the patients undergoing ablation for AF, and it exceeded the normal limit in one-third of the patients. Although NSE is a biomarker of neuronal injury, the clinical importance of this increase after AF ablation and its relationship with the left atrial diameter should be evaluated in a longitudinal study. |
format | Online Article Text |
id | pubmed-6259406 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-62594062018-11-30 Serum neuron-specific enolase, a marker of neuronal injury, increases after catheter ablation of atrial fibrillation Acibuca, Aynur Vurgun, Veysel Kutay Gerede, Demet Menekse Altin, Ali Timucin Gul, Inci Sule Candemir, Basar Isikay Togay, Canan Kilickap, Mustafa Akyurek, Omer J Int Med Res Clinical Research Reports OBJECTIVE: Catheter ablation of atrial fibrillation (AF) can lead to thromboembolic complications, especially stroke. We measured the periprocedural serum neuron-specific enolase (NSE) level, which is a biomarker of neuronal injury, after ablation of AF. METHODS: Forty-three patients with paroxysmal AF were prospectively enrolled before radiofrequency ablation. A neurological examination was performed before and after the procedure. The serum NSE level was determined before and at the end of the procedure and at 2, 24, and 48 h after the procedure. RESULTS: No patients developed new neurological deficits. However, the median (interquartile range) NSE level increased after ablation from 6.7 (3.87) ng/mL at baseline to 11.48 (5.3) ng/mL at 24 h postoperatively. The NSE level exceed the upper reference limit of normal (17 ng/mL) in 14 patients (33%), and these patients were found to have a larger left atrium. CONCLUSIONS: Serum NSE increased in most of the patients undergoing ablation for AF, and it exceeded the normal limit in one-third of the patients. Although NSE is a biomarker of neuronal injury, the clinical importance of this increase after AF ablation and its relationship with the left atrial diameter should be evaluated in a longitudinal study. SAGE Publications 2018-09-05 2018-11 /pmc/articles/PMC6259406/ /pubmed/30185093 http://dx.doi.org/10.1177/0300060518767768 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Clinical Research Reports Acibuca, Aynur Vurgun, Veysel Kutay Gerede, Demet Menekse Altin, Ali Timucin Gul, Inci Sule Candemir, Basar Isikay Togay, Canan Kilickap, Mustafa Akyurek, Omer Serum neuron-specific enolase, a marker of neuronal injury, increases after catheter ablation of atrial fibrillation |
title | Serum neuron-specific enolase, a marker of neuronal injury, increases after catheter ablation of atrial fibrillation |
title_full | Serum neuron-specific enolase, a marker of neuronal injury, increases after catheter ablation of atrial fibrillation |
title_fullStr | Serum neuron-specific enolase, a marker of neuronal injury, increases after catheter ablation of atrial fibrillation |
title_full_unstemmed | Serum neuron-specific enolase, a marker of neuronal injury, increases after catheter ablation of atrial fibrillation |
title_short | Serum neuron-specific enolase, a marker of neuronal injury, increases after catheter ablation of atrial fibrillation |
title_sort | serum neuron-specific enolase, a marker of neuronal injury, increases after catheter ablation of atrial fibrillation |
topic | Clinical Research Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259406/ https://www.ncbi.nlm.nih.gov/pubmed/30185093 http://dx.doi.org/10.1177/0300060518767768 |
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