Reference Values and Release Kinetics of B-Type Natriuretic Peptide Signal Peptide in Patients with Acute Myocardial Infarction

Author:

Liebetrau Christoph12,Gaede Luise12,Dörr Oliver3,Blumenstein Johannes12,Rosenburg Stefanie12,Hoffmann Jedrzej12,Troidl Christian12,Hamm Christian W123,Nef Holger M3,Möllmann Helge12,Richards A Mark45,Pemberton Chris J4

Affiliation:

1. Department of Cardiology, Kerckhoff Heart and Thorax Center, Bad Nauheim, Germany

2. DZHK (German Centre for Cardiovascular Research), partner site RheinMain, Frankfurt am Main, Germany

3. Department of Internal Medicine I, Division of Cardiology, University of Giessen, Giessen, Germany

4. Department of Medicine, Christchurch Heart Institute, University of Otago, Christchurch, New Zealand

5. Cardiovascular Research Institute, National University of Singapore, Singapore

Abstract

Abstract BACKGROUND The signal peptide for human B-type natriuretic peptide preprohormone (BNPsp), which is released from cardiomyocytes, is increased in plasma of patients with acute myocardial infarction (AMI); however, its exact release kinetics have not been defined. METHODS We measured BNPsp and high-sensitivity cardiac troponin T (hs-cTnT) in a reference group of individuals without structural heart disease (n = 285) and determined the release kinetics of these biomarkers in patients (n = 29) with hypertrophic obstructive cardiomyopathy undergoing transcoronary ablation of septal hypertrophy (TASH), a procedure allowing exact timing of onset of iatrogenic AMI. Blood samples were collected before TASH and at numerous preselected time points after TASH. RESULTS The reference median BNPsp concentration was 53.4 pmol/L [interquartile range (IQR) 47.0–61.0; 95th percentile 85.9 pmol/L; 99th percentile 116.3 pmol/L]. Baseline concentrations in patients undergoing TASH were higher than in the reference group [91.9 pmol/L (IQR 62.9–116.4); P < 0.0001]. BNPsp increased significantly, peaking at 15 min after induction of AMI [149.6 pmol/L (109.5–204.9) vs baseline; P = 0.004] and declining slowly thereafter, falling below the preprocedural value after 8 h (P = 0.014). hs-cTnT increased significantly 15 min after induction of AMI [26 ng/L (19–39) vs 18 ng/L (11–29); P = 0.001] and remained high at all later time points. CONCLUSIONS BNPsp concentrations increased immediately after AMI induction, providing early evidence of myocardial injury. The release kinetics of BNPsp differed from those of hs-cTnT. These findings provide information that should help in establishing the diagnostic value of BNPsp in the setting of early AMI.

Funder

William G. Kerkhoff-Stiftung Foundation

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

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