Key result
Clinical signs of heart failure in children with congenital heart defects or cardiomyopathy were associated with significantly higher plasma levels of P-BNP (263 vs 12.3 ng/L, p<0.001).
Why the study?
Are plasma levels of BNP and ANP associated with clinical signs of heart failure in children with congenital heart defects or cardiomyopathy?
Cross-Sectional (n=26)
Are plasma levels of BNP and ANP associated with clinical signs of heart failure in children with congenital heart defects or cardiomyopathy?
Answers are grounded in this paper and cite their sources.
Plasma levels of ANP and BNP are significantly elevated in children with clinical signs of heart failure, regardless of the underlying hemodynamic mechanism.
AIM: To study whether natriuretic peptide types B (BNP) and A (ANP) reflect clinical signs of heart failure (CSHF) in children with congenital heart defects or cardiomyopathy resulting in different types of haemodynamic situations, such as pressure overload in coarctation of the aorta (CoA), volume overload in ventricular septal defect (VSD) or systolic dysfunction in dilated cardiomyopathy (DCM). METHODS: Blood samples for plasma P-BNP and P-ANP were taken before procedures during regular investigation from 26 children (9 CoA, 11 VSD and 6 DCM). The ordinary paediatric cardiologist performed the cardiac evaluation and the data were retrieved from medical charts. CSHF was considered positive if two of the following criteria were fulfilled: reduced physical capacity, feeding disorders, dyspnoea, tachypnoea, hepatomegaly and oedema. The statistical methods were non-parametric. RESULTS: 0/9 children with CoA, 5/11 with VSD and 6/6 with DCM had CSHF. In children with CSHF, P-BNP and P-ANP were higher, 263 ng l(-1) (range 47.5-1300) and 303 ng l(-1) (range 168-466), than in those without CSHF, 12.3 ng l(-1) (range 4.8-30.8) and 42.9 ng l(-1) (range 13.7-189), respectively (p < 0.001, Mann-Whitney U-test), irrespective of the diagnosis. The same relationship was also found in the group of children with VSD. CONCLUSION: Plasma levels of ANP and BNP increase in children with CSHF. This increase is seen irrespective of whether it is due to systolic dysfunction, as in children with DCM, or to a volume overload with a normal systolic function, as in children with VSD.
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Westerlind et al. (2004) conducted a cross-sectional in Congenital heart defects or cardiomyopathy (n=26). Clinical signs of heart failure vs. No clinical signs of heart failure was evaluated on Plasma levels of P-BNP (ng/L) (p=<0.001). Clinical signs of heart failure in children with congenital heart defects or cardiomyopathy were associated with significantly higher plasma levels of P-BNP (263 vs 12.3 ng/L, p<0.001).
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