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

ESC Heart Failure

Stefan Störk¹  Tobias Gassenmaier¹  Dominik Schmitt¹  Anna Frey¹  Thorsten Bley¹  Georg Fette¹  Ulrich Hofmann¹  Valérie Boivin‐Jahns¹  Georg Ertl¹  Stefan Frantz¹  Roland Jahns¹  Almuth Marx¹  Sabine Herterich² 

[1] Comprehensive Heart Failure Center Würzburg University Hospital Würzburg Würzburg Germany;Division of Laboratory Medicine University Hospital Würzburg Würzburg Germany;

关键词: Blood coagulation factor XIII;    ST‐elevation myocardial infarction;    Healing and remodelling processes;    Cardiac magnetic resonance imaging;   

DOI  :  10.1002/ehf2.12774

来源: DOAJ

【 摘 要 】

Abstract 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.

【 授权许可】

Unknown