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Direct comparison of mid-regional pro-atrial natriuretic peptide with N-terminal pro B-type natriuretic peptide in the diagnosis of patients with atrial fibrillation and dyspnoea
  1. Jens Eckstein1,
  2. Mihael Potocki2,
  3. Karsten Murray2,
  4. Tobias Breidthardt1,
  5. Ronny Ziller2,
  6. Tamina Mosimann2,
  7. Theresia Klima1,
  8. Rebeca Hoeller2,
  9. Berit Moehring2,
  10. Seoung Mann Sou2,
  11. Maria Rubini Gimenez2,
  12. Nils G Morgenthaler3,
  13. Christian Mueller2
  1. 1Department of Medicine, University Hospital Basel, Basel, Switzerland
  2. 2Department of Cardiology, University Hospital Basel, Basel, Switzerland
  3. 3Institute for Experimental Endocrinology, Charité—Universitätsmedizin Berlin, Berlin, Germany
  1. Correspondence to Dr Jens Eckstein, Department of Medicine, University Hospital, Petersgraben 4, CH - 4031 – Basel, Switzerland; ecksteinj{at}uhbs.ch

Abstract

Objectives Due to different release mechanisms, mid-regional pro-atrial natriuretic peptide (MR proANP) may be superior to N-terminal pro-B-type natriuretic peptide (NT proBNP) in the diagnosis of acute heart failure (AHF) in patients with atrial fibrillation (AF). We compared MR proANP and NT proBNP for their diagnostic value in patients with AF and sinus rhythm (SR).

Design Prospective cohort study.

Setting University hospital, emergency department.

Patients 632 consecutive patients presenting with acute dyspnoea.

Main outcome measures MR proANP and NT proBNP plasma levels were determined. The diagnosis of AHF was adjudicated by two independent cardiologists using all available data. Patients received long-term follow-up.

Results AF was present in 151 patients (24%). MR proANP and NT proBNP levels were significantly higher in the AF group compared with the SR group (385 (258–598) versus 201 (89–375) pmol/l for MR proANP, p<0.001 and 4916 (2169–10285) versus 1177 (258–5166) pg/ml, p<0.001 for NT proBNP). Diagnostic accuracy in AF patients was similar for MR proANP (0.90, 95% CI 0.84 to 0.95) and NT proBNP (0.89, 95% CI 0.81 to 0.96). Optimal cut-off levels in AF patients were significantly higher compared with the optimal cut-off levels for patients in SR (MR proANP 240 vs 200 pmol/l; NT proBNP 2670 vs 1500 pg/ml respectively). After adjustment in multivariable Cox proportional hazard analysis, MR proANP strongly predicted one-year all-cause mortality (HR=1.13 (1.09–1.17), per 100 pmol/l increase, p<0.001).

Conclusion In AF patients, NT proBNP and MR proANP have similar diagnostic value for the diagnosis of AHF. The rhythm at presentation has to be taken into account because plasma levels of both peptides are significantly higher in patients with AF compared with SR.

  • Atrial fibrillation
  • MR proANP
  • NT proBNP
  • heart failure
  • sensitivity and specificity
  • arrhythmias
  • endocardial map
  • implantable cardioverter defibrillator
  • pacemakers
  • coronary artery disease
  • chest pain clinic
  • mortality statistics
  • congestive heart failure
  • valvular disease
  • mitral regurgitation
  • myocardial ischaemia and infarction
  • interventional cardiology
  • acute coronary syndrome
  • intensive care
  • natriuretic peptides
  • acute myocardial infarction

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Footnotes

  • JE and MP equal contribution to this work.

  • Funding Christian Mueller, as principal investigator, was supported by grants from the Swiss National Science Foundation (PP00B-102853), the Swiss Heart Foundation, the University of Basel, Abbott, ALERE, BRAHMS, and Pronota. In addition, Christian Mueller received lecture fees from Abbott, ALERE, BRAHMS, Novartis and Roche. Jens Eckstein was supported by research grants from the Swiss National Science Foundation, the Marie Curie Program and the University of Basel, and travel grants from Medtronic, St Jude Medical and Boehringer Ingelheim. Mihael Potocki has received speaker honoraria from Abbott, BRAHMS and Roche. For the other authors no conflict of interest exists.

  • Competing interests None.

  • Ethics approval Ethics approval provided by Local Ethics Committee University Basel.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data sharing statement At present, there is no additional unpublished data of this particular study available to any other scientists/journals.

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