Cardiac biomarkers in pediatric CKD-a prospective follow-up study

Ylva Tranæus Lindblad1,2,3, Georgios Vavilis4,5, Milan Chromek6,7

  • 1Divisions of Pediatrics, CLINTEC, Karolinska Institutet, Stockholm, Sweden. ylva.tranaeus@ki.se.

Insights

Cardiac biomarkers N-terminal pro-B-type natriuretic peptide (NT-proBNP) and high-sensitive cardiac-specific troponin T (hs-cTnT) are elevated in pediatric chronic kidney disease (CKD) patients. NT-proBNP may indicate early subclinical myocardial damage, linked to left ventricular mass index.

Area of Science:

  • Pediatric Nephrology
  • Cardiology
  • Biomarker Research

Background:

  • N-terminal pro-B-type natriuretic peptide (NT-proBNP) and high-sensitive cardiac-specific troponin T (hs-cTnT) are linked to adverse cardiac outcomes in adult chronic kidney disease (CKD).
  • Limited data exists on these cardiac markers in pediatric CKD populations.

Purpose of the Study:

  • To investigate longitudinal levels of NT-proBNP and hs-cTnT in pediatric CKD patients.
  • To assess associations between these markers, kidney function, cardiovascular risk, and echocardiographic parameters.

Main Methods:

  • Analyzed longitudinal NT-proBNP and hs-cTnT in 48 pediatric patients (22 CKD, 26 CKD-transplanted).
  • Assessed patterns over 1 and 3 years, correlating with GFR, cardiovascular risk markers, and echocardiographic findings (LVMI, diastolic function).

Main Results:

  • Elevated NT-proBNP and hs-cTnT were observed in pediatric CKD and CKD-transplanted patients.
  • High NT-proBNP correlated with lower GFR and elevated LVMI; this association persisted with GFR-adjusted NT-proBNP.
  • High hs-cTnT correlated with lower GFR and impaired LV diastolic function.

Conclusions:

  • NT-proBNP and hs-cTnT are elevated in pediatric CKD and CKD-transplanted patients.
  • GFR-adjusted NT-proBNP may serve as a marker for early subclinical myocardial damage, associated with LVMI.
  • Further research is warranted to understand the clinical implications of these findings in pediatric CKD.
Abstract

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