N-Terminal-pro-b-Type natriuretic peptide levels and cardiac hemosiderosis in adolescent β-Thalassemia major patients

Research output: Contribution to journalArticlepeer-review

Abstract

Background: Iron-induced cardiomyopathy remains the leading cause of mortality in patients with β-Thalassemia major. Iron overload cardiomyopathy, which may be reversible through iron chelation, is characterized by early diastolic dysfunction. Amino-Terminal pro-brain natriuretic peptide (NT-proBNP) is a sensitive biomarker of diastolic dysfunction. Aim: The aim of the study is to evaluate the diagnostic value of NT-proBNP as a surrogate marker of iron overload examined with magnetic resonance imaging T2-star (MRI T2∗). Methods: Sixty-eight β-Thalassemia major patients (10-18 years) with no signs of heart failure underwent NT-proBNP measurement before routine transfusion. All participants prospectively underwent cardiac MRI T2∗ examination within 3 months (median 19 days). Patients were divided as cardiac hemosiderosis (cardiac MRI T2∗ <20 ms) and nonhemosiderosis (cardiac MRI T2∗ >20 ms). Results: Of 68 patients, the male-To-female ratio was 1:1.1 and the median age was 14.1 years (range: 10-17.8 years). NT-proBNP levels were not different between hemosiderosis and nonhemosiderosis patients (P = 0.233). Further receiver operating characteristic analysis resulted in no significant correlation of NT-proBNP and MRI T2∗ (area under the curve 0.393, P = 0.233). Conclusion: Measurement of NT-proBNP levels cannot be used for early detection of cardiac iron overload in adolescent with β-Thalassemia major.

Original languageEnglish
Pages (from-to)32-37
Number of pages6
JournalAnnals of Pediatric Cardiology
Volume12
Issue number1
DOIs
Publication statusPublished - 1 Jan 2019

Keywords

  • Adolescent
  • amino-Terminal pro-brain natriuretic peptide
  • magnetic resonance imaging T2-star
  • β-Thalassemia major

Fingerprint

Dive into the research topics of 'N-Terminal-pro-b-Type natriuretic peptide levels and cardiac hemosiderosis in adolescent β-Thalassemia major patients'. Together they form a unique fingerprint.

Cite this