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Coagulation factor XIII activity predicts left ventricular remodelling after acute myocardial infarction

AIMS: Acute myocardial infarction (MI) is the major cause of chronic heart failure. The activity of blood coagulation factor XIII (FXIIIa) plays an important role in rodents as a healing factor after MI, whereas its role in healing and remodelling processes in humans remains unclear. We prospectivel...

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Autores principales: Frey, Anna, Gassenmaier, Tobias, Hofmann, Ulrich, Schmitt, Dominik, Fette, Georg, Marx, Almuth, Herterich, Sabine, Boivin‐Jahns, Valérie, Ertl, Georg, Bley, Thorsten, Frantz, Stefan, Jahns, Roland, Störk, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524135/
https://www.ncbi.nlm.nih.gov/pubmed/32548915
http://dx.doi.org/10.1002/ehf2.12774
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author Frey, Anna
Gassenmaier, Tobias
Hofmann, Ulrich
Schmitt, Dominik
Fette, Georg
Marx, Almuth
Herterich, Sabine
Boivin‐Jahns, Valérie
Ertl, Georg
Bley, Thorsten
Frantz, Stefan
Jahns, Roland
Störk, Stefan
author_facet Frey, Anna
Gassenmaier, Tobias
Hofmann, Ulrich
Schmitt, Dominik
Fette, Georg
Marx, Almuth
Herterich, Sabine
Boivin‐Jahns, Valérie
Ertl, Georg
Bley, Thorsten
Frantz, Stefan
Jahns, Roland
Störk, Stefan
author_sort Frey, Anna
collection PubMed
description AIMS: Acute myocardial infarction (MI) is the major cause of chronic heart failure. The activity of blood coagulation factor XIII (FXIIIa) plays an important role in rodents as a healing factor after MI, whereas its role in healing and remodelling processes in humans remains unclear. We prospectively evaluated the relevance of FXIIIa after acute MI as a potential early prognostic marker for adequate healing. METHODS AND RESULTS: This monocentric prospective cohort study investigated cardiac remodelling in patients with ST‐elevation MI and followed them up for 1 year. Serum FXIIIa was serially assessed during the first 9 days after MI and after 2, 6, and 12 months. Cardiac magnetic resonance imaging was performed within 4 days after MI (Scan 1), after 7 to 9 days (Scan 2), and after 12 months (Scan 3). The FXIII valine‐to‐leucine (V34L) single‐nucleotide polymorphism rs5985 was genotyped. One hundred forty‐six patients were investigated (mean age 58 ± 11 years, 13% women). Median FXIIIa was 118% (quartiles, 102–132%) and dropped to a trough on the second day after MI: 109% (98–109%; P < 0.001). FXIIIa recovered slowly over time, reaching the baseline level after 2 to 6 months and surpassed baseline levels only after 12 months: 124% (110–142%). The development of FXIIIa after MI was independent of the genotype. FXIIIa on Day 2 was strongly and inversely associated with the relative size of MI in Scan 1 (Spearman's ρ = –0.31; P = 0.01) and Scan 3 (ρ = –0.39; P < 0.01) and positively associated with left ventricular ejection fraction: ρ = 0.32 (P < 0.01) and ρ = 0.24 (P = 0.04), respectively. CONCLUSIONS: FXIII activity after MI is highly dynamic, exhibiting a significant decline in the early healing period, with reconstitution 6 months later. Depressed FXIIIa early after MI predicted a greater size of MI and lower left ventricular ejection fraction after 1 year. The clinical relevance of these findings awaits to be tested in a randomized trial.
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spelling pubmed-75241352020-10-02 Coagulation factor XIII activity predicts left ventricular remodelling after acute myocardial infarction Frey, Anna Gassenmaier, Tobias Hofmann, Ulrich Schmitt, Dominik Fette, Georg Marx, Almuth Herterich, Sabine Boivin‐Jahns, Valérie Ertl, Georg Bley, Thorsten Frantz, Stefan Jahns, Roland Störk, Stefan ESC Heart Fail Original Research Articles AIMS: Acute myocardial infarction (MI) is the major cause of chronic heart failure. The activity of blood coagulation factor XIII (FXIIIa) plays an important role in rodents as a healing factor after MI, whereas its role in healing and remodelling processes in humans remains unclear. We prospectively evaluated the relevance of FXIIIa after acute MI as a potential early prognostic marker for adequate healing. METHODS AND RESULTS: This monocentric prospective cohort study investigated cardiac remodelling in patients with ST‐elevation MI and followed them up for 1 year. Serum FXIIIa was serially assessed during the first 9 days after MI and after 2, 6, and 12 months. Cardiac magnetic resonance imaging was performed within 4 days after MI (Scan 1), after 7 to 9 days (Scan 2), and after 12 months (Scan 3). The FXIII valine‐to‐leucine (V34L) single‐nucleotide polymorphism rs5985 was genotyped. One hundred forty‐six patients were investigated (mean age 58 ± 11 years, 13% women). Median FXIIIa was 118% (quartiles, 102–132%) and dropped to a trough on the second day after MI: 109% (98–109%; P < 0.001). FXIIIa recovered slowly over time, reaching the baseline level after 2 to 6 months and surpassed baseline levels only after 12 months: 124% (110–142%). The development of FXIIIa after MI was independent of the genotype. FXIIIa on Day 2 was strongly and inversely associated with the relative size of MI in Scan 1 (Spearman's ρ = –0.31; P = 0.01) and Scan 3 (ρ = –0.39; P < 0.01) and positively associated with left ventricular ejection fraction: ρ = 0.32 (P < 0.01) and ρ = 0.24 (P = 0.04), respectively. CONCLUSIONS: FXIII activity after MI is highly dynamic, exhibiting a significant decline in the early healing period, with reconstitution 6 months later. Depressed FXIIIa early after MI predicted a greater size of MI and lower left ventricular ejection fraction after 1 year. The clinical relevance of these findings awaits to be tested in a randomized trial. John Wiley and Sons Inc. 2020-06-17 /pmc/articles/PMC7524135/ /pubmed/32548915 http://dx.doi.org/10.1002/ehf2.12774 Text en © 2020 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of the European Society of Cardiology This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Research Articles
Frey, Anna
Gassenmaier, Tobias
Hofmann, Ulrich
Schmitt, Dominik
Fette, Georg
Marx, Almuth
Herterich, Sabine
Boivin‐Jahns, Valérie
Ertl, Georg
Bley, Thorsten
Frantz, Stefan
Jahns, Roland
Störk, Stefan
Coagulation factor XIII activity predicts left ventricular remodelling after acute myocardial infarction
title Coagulation factor XIII activity predicts left ventricular remodelling after acute myocardial infarction
title_full Coagulation factor XIII activity predicts left ventricular remodelling after acute myocardial infarction
title_fullStr Coagulation factor XIII activity predicts left ventricular remodelling after acute myocardial infarction
title_full_unstemmed Coagulation factor XIII activity predicts left ventricular remodelling after acute myocardial infarction
title_short Coagulation factor XIII activity predicts left ventricular remodelling after acute myocardial infarction
title_sort coagulation factor xiii activity predicts left ventricular remodelling after acute myocardial infarction
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524135/
https://www.ncbi.nlm.nih.gov/pubmed/32548915
http://dx.doi.org/10.1002/ehf2.12774
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