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Percutaneous Closure of Left Atrial Appendage affects Mid-Term Release of MR-proANP

The left atrial appendage (LAA) represents both a predisposing source of thrombus formation and of neuro-humoral haemostasis. This study aims to evaluate changes of biomarker expression before and after successful percutaneous closure of the LAA. Patients with atrial fibrillation and contraindicatio...

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Autores principales: Behnes, Michael, Sartorius, Benjamin, Wenke, Annika, Lang, Siegfried, Hoffmann, Ursula, Fastner, Christian, Borggrefe, Martin, Roth, Thomas, Triebel, Jakob, Bertsch, Thomas, Akin, Ibrahim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5567360/
https://www.ncbi.nlm.nih.gov/pubmed/28831085
http://dx.doi.org/10.1038/s41598-017-08999-4
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author Behnes, Michael
Sartorius, Benjamin
Wenke, Annika
Lang, Siegfried
Hoffmann, Ursula
Fastner, Christian
Borggrefe, Martin
Roth, Thomas
Triebel, Jakob
Bertsch, Thomas
Akin, Ibrahim
author_facet Behnes, Michael
Sartorius, Benjamin
Wenke, Annika
Lang, Siegfried
Hoffmann, Ursula
Fastner, Christian
Borggrefe, Martin
Roth, Thomas
Triebel, Jakob
Bertsch, Thomas
Akin, Ibrahim
author_sort Behnes, Michael
collection PubMed
description The left atrial appendage (LAA) represents both a predisposing source of thrombus formation and of neuro-humoral haemostasis. This study aims to evaluate changes of biomarker expression before and after successful percutaneous closure of the LAA. Patients with atrial fibrillation and contraindication for oral anticoagulant therapy were enrolled. Blood samples were taken within 24 hours before (T1) and at least 6 months (mid-term) (T2) after successful implantation of LAA occlusion devices. Blood levels of high sensitivity troponin I and T (hsTnI, hsTnT), aminoterminal pro-brain natriuretic peptide (NT-proBNP) and mid-regional pro-atrial natriuretic peptide (MR-proANP) were evaluated at both time points. A total of 42 patients with successful percutaneous LAA closure were included. Median mid-term follow-up was of 183 days. HsTnT, hsTnI and NT-proBNP did not show any significant differences over time. Serum levels of MR-proANP increased significantly between immediate pre-intervention (T1: median = 245.7 pmol/l, IQR 155.8–361.3 pmol/l) and at mid-term follow-up (T2: median = 254 pmol/l, IQR 183.4–396.4 pmol/l) (p = 0.037). These results indicate, that percutaneous LAA closure affects neuro-humoral haemostasis by increasing MR-proANP serum levels at mid-term follow-up.
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spelling pubmed-55673602017-09-01 Percutaneous Closure of Left Atrial Appendage affects Mid-Term Release of MR-proANP Behnes, Michael Sartorius, Benjamin Wenke, Annika Lang, Siegfried Hoffmann, Ursula Fastner, Christian Borggrefe, Martin Roth, Thomas Triebel, Jakob Bertsch, Thomas Akin, Ibrahim Sci Rep Article The left atrial appendage (LAA) represents both a predisposing source of thrombus formation and of neuro-humoral haemostasis. This study aims to evaluate changes of biomarker expression before and after successful percutaneous closure of the LAA. Patients with atrial fibrillation and contraindication for oral anticoagulant therapy were enrolled. Blood samples were taken within 24 hours before (T1) and at least 6 months (mid-term) (T2) after successful implantation of LAA occlusion devices. Blood levels of high sensitivity troponin I and T (hsTnI, hsTnT), aminoterminal pro-brain natriuretic peptide (NT-proBNP) and mid-regional pro-atrial natriuretic peptide (MR-proANP) were evaluated at both time points. A total of 42 patients with successful percutaneous LAA closure were included. Median mid-term follow-up was of 183 days. HsTnT, hsTnI and NT-proBNP did not show any significant differences over time. Serum levels of MR-proANP increased significantly between immediate pre-intervention (T1: median = 245.7 pmol/l, IQR 155.8–361.3 pmol/l) and at mid-term follow-up (T2: median = 254 pmol/l, IQR 183.4–396.4 pmol/l) (p = 0.037). These results indicate, that percutaneous LAA closure affects neuro-humoral haemostasis by increasing MR-proANP serum levels at mid-term follow-up. Nature Publishing Group UK 2017-08-22 /pmc/articles/PMC5567360/ /pubmed/28831085 http://dx.doi.org/10.1038/s41598-017-08999-4 Text en © The Author(s) 2017 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Behnes, Michael
Sartorius, Benjamin
Wenke, Annika
Lang, Siegfried
Hoffmann, Ursula
Fastner, Christian
Borggrefe, Martin
Roth, Thomas
Triebel, Jakob
Bertsch, Thomas
Akin, Ibrahim
Percutaneous Closure of Left Atrial Appendage affects Mid-Term Release of MR-proANP
title Percutaneous Closure of Left Atrial Appendage affects Mid-Term Release of MR-proANP
title_full Percutaneous Closure of Left Atrial Appendage affects Mid-Term Release of MR-proANP
title_fullStr Percutaneous Closure of Left Atrial Appendage affects Mid-Term Release of MR-proANP
title_full_unstemmed Percutaneous Closure of Left Atrial Appendage affects Mid-Term Release of MR-proANP
title_short Percutaneous Closure of Left Atrial Appendage affects Mid-Term Release of MR-proANP
title_sort percutaneous closure of left atrial appendage affects mid-term release of mr-proanp
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5567360/
https://www.ncbi.nlm.nih.gov/pubmed/28831085
http://dx.doi.org/10.1038/s41598-017-08999-4
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