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Published on: April 27, 2019
Subclinical cardiovascular changes in pediatric solid organ transplant recipients: A systematic review and
Yasser Al Nasser1,2, Marta C Moura1,2, Luc Mertens2,3
1Division of Gastroenterology, Hepatology and Nutrition, Hospital for Sick Children, Toronto, ON, Canada.
Insights
Pediatric solid organ transplant recipients, particularly kidney transplant patients, show increased subclinical cardiovascular changes like elevated carotid intima-media thickness (cIMT). Further research is needed to assess long-term cardiovascular risks in these young patients.
Area of Science:
- Cardiology
- Pediatric Nephrology
- Transplantation Medicine
Background:
- Cardiovascular (CV) disease is a significant cause of death in adult transplant recipients.
- While cardiometabolic risk factors are common in pediatric transplant patients, subclinical CV changes are not well-established.
- Measures like carotid intima-media thickness (cIMT), pulse wave velocity (pWV), and coronary artery calcification (CAC) indicate subclinical CV disease and predict future events in adults.
Purpose of the Study:
- To systematically review and meta-analyze the prevalence of subclinical CV changes (cIMT, pWV, CAC) in pediatric solid organ transplant recipients.
- To compare CV health in pediatric transplant recipients versus healthy controls.
Main Methods:
- Systematic review and meta-analysis of studies indexed in MEDLINE and EMBASE.
- Inclusion criteria: studies evaluating cIMT, central pWV, and CAC in pediatric recipients of kidney, lung, intestine, and liver transplants.
- Nine studies involving 259 patients and 685 controls were analyzed.
Main Results:
- The mean cIMT was significantly higher in transplant recipients than in controls (mean difference = 0.05 mm, p < 0.0001).
- The pooled prevalence of elevated cIMT was 56.0%.
- One study indicated increased vascular stiffness (pWV) in transplant recipients; no studies reported on CAC.
Conclusions:
- Pediatric kidney transplantation is associated with a higher prevalence of subclinical CV changes compared to healthy children.
- Limited data exist on subclinical CV disease post-pediatric solid organ transplantation.
- Longitudinal studies are essential to determine long-term CV morbidity and mortality risks in these children.
Abstract:
CV disease is a major cause of morbidity and mortality following solid organ transplantation in adults. While the prevalence of multiple cardiometabolic risk factors is increased in pediatric solid organ transplant recipients, it is not clear whether they have subclinical CV changes. cIMT, central pWV, and CAC are indicative of subclinical CV disease, and, in adults, predict future CV events. The objective of this systematic review and meta-analysis was to investigate the prevalence of subclinical CV changes, as measured by cIMT, pWV, and CAC among pediatric solid organ transplant recipients. We searched MEDLINE(®) and EMBASE and conducted meta-analysis for studies that evaluated cIMT, central pWV, and CAC among pediatric solid organ transplant recipients (kidney, lung, intestine and liver). The search identified nine eligible studies that included a total of 259 patients and 685 healthy controls. Eight studies reported on kidney transplant recipients and one study on a combined cohort of kidney and liver transplant recipients. The mean cIMT of transplant recipients was significantly higher than that of healthy controls (mean difference = 0.05 mm, 95% CI 0.02-0.07; p < 0.0001) with an estimated pooled prevalence of elevated cIMT of 56.0% (95% CI 17.0-95.0). The one study that assessed pWV showed increased vascular stiffness in transplant recipients compared to healthy controls. No studies assessing for CAC were found. There were limited data regarding subclinical CV disease following pediatric solid organ transplantation. In conclusion, kidney transplantation in childhood is associated with a higher prevalence of subclinical CV changes compared to healthy children. Longitudinal studies are needed to determine whether children have increased CV morbidity and mortality after transplantation.
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