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Abnormal left ventricular mass and aortic distensibility in pediatric dialysis patients
Renee F Robinson1, Milap C Nahata, Elizabeth Sparks
1Children's Research Institute, 700 Children's Drive, Columbus, OH 43205, USA. Robinsonr@pediatrics.ohio-state.edu
Insights
Children with end-stage renal disease (ESRD) show cardiovascular damage, including increased left ventricular mass (LVM) and abnormal aortic distensibility (AD). Hemodialysis (HD) patients had greater vascular stiffness than peritoneal dialysis (PD) patients.
Area of Science:
- Pediatric Nephrology
- Cardiovascular Research
- Renal Disease Pathophysiology
Background:
- Cardiovascular disease (CVD) is a major concern in end-stage renal disease (ESRD).
- Pathophysiological processes affecting cardiovascular function in adult ESRD patients are also present in pediatric ESRD.
- Established correlations between left ventricular mass (LVM) and aortic distensibility (AD) in adult hemodialysis (HD) patients are not well-defined in pediatric populations.
Purpose of the Study:
- To investigate cardiovascular damage, specifically LVM and AD, in pediatric ESRD patients undergoing HD or peritoneal dialysis (PD).
- To analyze the relationship between AD, LVM, LVMI, blood pressure (BP), and demographic factors in pediatric ESRD patients.
- To compare cardiovascular parameters between children on HD and PD.
Main Methods:
- Retrospective study analyzing LVM, LVMI, and AD in pediatric ESRD patients (n=9 HD, n=9 PD) and a control group.
- Comparison of cardiovascular parameters between dialysis modalities and a control population.
- Analysis of correlations between AD, LVM, LVMI, pre-dialysis and post-dialysis BP, and demographic factors.
Main Results:
- Both LVM and AD were significantly higher in the dialysis population compared to controls.
- LVM and LVMI did not differ significantly between HD and PD groups.
- Aortic distensibility (AD) was significantly lower in the HD group compared to the PD group, indicating greater vascular stiffness in HD patients.
Conclusions:
- Pediatric ESRD patients on dialysis exhibit increased LVM and abnormal vascular stiffness (reduced AD).
- Vascular stiffness is more pronounced in children undergoing HD compared to PD.
- Further research is needed to understand the impact of BP control, uremia, and other factors on these cardiovascular abnormalities in pediatric ESRD.
Abstract:
There is ample evidence that the same pathophysiological processes that affect cardiovascular function in adults with end-stage renal disease (ESRD) also operate in children with ESRD. In adults undergoing hemodialysis (HD), a good correlation has been established between left ventricular mass (LVM) and aortic distensibility (AD) as markers of cardiovascular disease progression; however, this correlation has not been established in children. Therefore, in this retrospective study we investigated some aspects of cardiovascular damage (i.e., LVM, LVMI, and AD) in children with ESRD undergoing HD (n=9) or peritoneal dialysis (PD, n=9), and analyzed the relationship between AD, LVM, LVMI, pre-dialysis, post-dialysis blood pressure (BP), and demographic factors in children and adolescents with ESRD. Both LVM and AD were significantly greater in the dialysis population than in a control population derived from our institutional files (P=0.015, P=0.001). LVM and LVMI in children undergoing HD (92.9+/-83.7 g, 80.1+/-31.1 g/cm) were not statistically different from the values in children on PD (130.0+/-89.2 g, 89.6+/-35.9 g/cm), (P=0.3, P=0.5). AD in children on HD (2.2+/-0.55 cm2* dynes(-1*(10-6)) was significantly lower than in children on PD (2.7+/-0.54 cm2* dynes(-1*(10-6)), (P=0.01). The findings in this study confirm earlier studies that demonstrated that LVMI is greater in children on dialysis. This study also demonstrates that abnormal vascular stiffness, as defined by AD, is present in these children. The degree of vascular stiffness in children receiving HD is greater than in children receiving PD. However, further study is needed to address how control of BP, uremia, and other factors may affect these abnormalities in children with ESRD.
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