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Eur Heart J. 2014 Jan;35(1):33-41. doi: 10.1093/eurheartj/ehs229. Epub 2012 Jul 26.

Beta-adrenergic adaptation in paediatric idiopathic dilated cardiomyopathy.

Author information

1
Department of Pediatrics, University of Colorado School of Medicine, Children's Hospital Colorado, Aurora, CO, USA.

Abstract

BACKGROUND:

Although the pathophysiology and treatment of adult heart failure (HF) are well studied, HF in children remains poorly understood. In adults, adrenergic receptor (AR)-mediated adaptation plays a central role in cardiac abnormalities in HF, and these patients respond well to β-blocker (BB) therapy. However, in children with HF, there is a growing body of literature suggesting a lack of efficacy of adult HF therapies. Due to these unanticipated differences in response to therapy and the paucity of data regarding the molecular adaptation of the paediatric heart, we investigated the molecular characteristics of HF in children.

METHODS AND RESULTS:

Explanted hearts from adults and children with idiopathic dilated cardiomyopathy and non-failing controls were used in the study. Our results show that the molecular characteristics of paediatric HF are strikingly different from their adult counterparts. These differences include: (i) down-regulation of β1- and β2-AR in children, whereas β2-AR expression is maintained in adults; (ii) up-regulation of connexin43 in children, whereas down-regulation is observed in adults; (iii) no differences in phosphatase expression, whereas up-regulation is observed in adults; (iv) no decrease in the phosphorylation of phospholamban at the Ser16 or Thr17 sites in children, which are known characteristics of adult HF.

CONCLUSION:

There is a different adaptation of β-AR and adrenergic signalling pathways in children with HF compared with adults. Our results begin to address the disparities in cardiovascular research specific to children and suggest that age-related differences in adaptation could influence the response to therapy. These findings could lead to a paradigm shift in the contemporary management of children with HF.

KEYWORDS:

CaMK; Fetal gene programme; Paediatric dilated cardiomyopathy; Phosphatase; β-Adrenergic receptor

PMID:
22843448
PMCID:
PMC3877432
DOI:
10.1093/eurheartj/ehs229
[Indexed for MEDLINE]
Free PMC Article

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