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Apelin: A novel prognostic predictor for atrial fibrillation recurrence after pulmonary vein isolation

Apelin, the ligand for the APJ receptor, is involved in the pathogenesis of atrial fibrillation (AF). However, whether serum apelin can predict the recurrence of AF after pulmonary vein isolation (PVI) has not been determined. A prospective cohort study was performed in patients with AF (but without...

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Autores principales: Wang, Ya Zhu, Fan, Jinqi, Zhong, Bin, Xu, Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6181607/
https://www.ncbi.nlm.nih.gov/pubmed/30278567
http://dx.doi.org/10.1097/MD.0000000000012580
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author Wang, Ya Zhu
Fan, Jinqi
Zhong, Bin
Xu, Qiang
author_facet Wang, Ya Zhu
Fan, Jinqi
Zhong, Bin
Xu, Qiang
author_sort Wang, Ya Zhu
collection PubMed
description Apelin, the ligand for the APJ receptor, is involved in the pathogenesis of atrial fibrillation (AF). However, whether serum apelin can predict the recurrence of AF after pulmonary vein isolation (PVI) has not been determined. A prospective cohort study was performed in patients with AF (but without structural heart disease) who were undergoing first-time PVI. Serum apelin-12 was measured by enzyme-linked immunosorbent assay. Echocardiographic examination was performed at baseline, 3 months, and 6 months after PVI. Patients were followed up for 6 months after PVI, and the association between baseline apelin-12 and AF recurrence (early recurrence: within 3 months after ablation; late recurrence: 3–6 months after ablation) was analyzed. A total of 61 patients were included in the study. Baseline serum level of apelin-12 was significant lower in patients with early (median [interquartile range]: 1844 [1607–2061] vs 2197 [1895–2455] ng/L, P = .01) and late (1639 [1524–1853] vs 1923 [1741–2303] ng/L, P = .02) AF recurrence compared with patients without these events. Results of Cox stepwise multivariate analysis demonstrated that lower baseline apelin-12 (<2265 ng/L) was independently associated with increased AF recurrence within 6 months after PVI (P < .05). The specificity and positive predictive value of apelin-12 for AF recurrence were significantly higher than those of baseline N-terminal brain proBNP (60.4% vs 28.6%, P < .001; 58.8% vs 34.4%, P = .01), although the sensitivity and negative predictive value were similar. Reduced baseline serum apelin-12 may be an independent risk factor for the recurrence of AF after PVI in patients without structural heart disease.
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spelling pubmed-61816072018-10-15 Apelin: A novel prognostic predictor for atrial fibrillation recurrence after pulmonary vein isolation Wang, Ya Zhu Fan, Jinqi Zhong, Bin Xu, Qiang Medicine (Baltimore) Research Article Apelin, the ligand for the APJ receptor, is involved in the pathogenesis of atrial fibrillation (AF). However, whether serum apelin can predict the recurrence of AF after pulmonary vein isolation (PVI) has not been determined. A prospective cohort study was performed in patients with AF (but without structural heart disease) who were undergoing first-time PVI. Serum apelin-12 was measured by enzyme-linked immunosorbent assay. Echocardiographic examination was performed at baseline, 3 months, and 6 months after PVI. Patients were followed up for 6 months after PVI, and the association between baseline apelin-12 and AF recurrence (early recurrence: within 3 months after ablation; late recurrence: 3–6 months after ablation) was analyzed. A total of 61 patients were included in the study. Baseline serum level of apelin-12 was significant lower in patients with early (median [interquartile range]: 1844 [1607–2061] vs 2197 [1895–2455] ng/L, P = .01) and late (1639 [1524–1853] vs 1923 [1741–2303] ng/L, P = .02) AF recurrence compared with patients without these events. Results of Cox stepwise multivariate analysis demonstrated that lower baseline apelin-12 (<2265 ng/L) was independently associated with increased AF recurrence within 6 months after PVI (P < .05). The specificity and positive predictive value of apelin-12 for AF recurrence were significantly higher than those of baseline N-terminal brain proBNP (60.4% vs 28.6%, P < .001; 58.8% vs 34.4%, P = .01), although the sensitivity and negative predictive value were similar. Reduced baseline serum apelin-12 may be an independent risk factor for the recurrence of AF after PVI in patients without structural heart disease. Wolters Kluwer Health 2018-09-28 /pmc/articles/PMC6181607/ /pubmed/30278567 http://dx.doi.org/10.1097/MD.0000000000012580 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Research Article
Wang, Ya Zhu
Fan, Jinqi
Zhong, Bin
Xu, Qiang
Apelin: A novel prognostic predictor for atrial fibrillation recurrence after pulmonary vein isolation
title Apelin: A novel prognostic predictor for atrial fibrillation recurrence after pulmonary vein isolation
title_full Apelin: A novel prognostic predictor for atrial fibrillation recurrence after pulmonary vein isolation
title_fullStr Apelin: A novel prognostic predictor for atrial fibrillation recurrence after pulmonary vein isolation
title_full_unstemmed Apelin: A novel prognostic predictor for atrial fibrillation recurrence after pulmonary vein isolation
title_short Apelin: A novel prognostic predictor for atrial fibrillation recurrence after pulmonary vein isolation
title_sort apelin: a novel prognostic predictor for atrial fibrillation recurrence after pulmonary vein isolation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6181607/
https://www.ncbi.nlm.nih.gov/pubmed/30278567
http://dx.doi.org/10.1097/MD.0000000000012580
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