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Right Atrial Myocardial Remodeling in Children With Atrial Septal Defect Involves Inflammation, Growth, Fibrosis, and
Hatem Rouatbi1, Nesrine Farhat1, Ruth Heying2
1Department of Pediatrics & Pediatric Cardiology, University Hospital Liège, Liège, Belgium.
Insights
Large atrial septum defects (ASD) cause right atrial remodeling through inflammation, fibrosis, and apoptosis. These cellular changes in children with ASD may lead to long-term health issues.
Area of Science:
- Cardiovascular Biology
- Pediatric Cardiology
- Molecular Medicine
Background:
- Large atrial septum defects (ASD) lead to right-sided heart chamber dilation due to volume overload.
- The precise cellular mechanisms driving this myocardial remodeling remain largely unknown.
Purpose of the Study:
- To investigate the cellular mechanisms underlying right atrial remodeling in children with large ASD.
- To determine the roles of inflammation, fibrosis, and apoptosis in this process.
Main Methods:
- Gene expression analysis (RT-PCR) of myocardial biopsies from 12 children with large ASD.
- Immunohistochemistry to detect cytokines and TUNEL assay for apoptosis assessment.
Main Results:
- All patients showed cellular responses including stress protection, inflammation, growth, angiogenesis, fibrosis, and apoptosis.
- The average apoptotic index was 0.3%.
Conclusions:
- Right atrial remodeling in children with ASD involves complex cellular mechanisms.
- These mechanisms include gene expression related to cell protection, inflammation, fibrosis, and apoptosis, potentially contributing to long-term morbidity.
Abstract:
Introduction: Myocardial remodeling due to large atrial septum defect (ASD) is macroscopically characterized by dilation of the right-sided cardiac cavities secondary to volume overload, the cellular mechanisms of which are not yet understood. We postulated that inflammation, fibrosis, and cell death are actors of right atrial remodeling secondary to ASD. Patients and Methods: In 12 children with large ASD (median age: 63 months), expression of genes coding for proteins involved in the response to cell stress and -protection, inflammation, growth and angiogenesis, fibrosis, and apoptosis was assessed by RT-PCR in right atrial myocardial biopsies taken during cardiac surgery. The presence of cytokines in myocardial cells was confirmed by immunohistochemistry and effective apoptosis by TUNEL assay. Results: In all patients investigated, a cellular response to early mechanical stress with the initiation of early protective mechanisms, of inflammation (and its control), -growth, and -angiogenesis, of fibrosis and apoptosis was present. The apoptotic index assessed by TUNEL assay averaged 0.3%. Conclusions: In children with large ASD, macroscopic right atrial remodeling relates to cellular mechanisms involving the expression of numerous genes that either still act to protect cells and tissues but that also harm as they initiate and/or sustain inflammation, fibrosis, and cell death by apoptosis. This may contribute to long term morbidity in patients with ASD.
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