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Author Spotlight: Evaluating Therapeutic Strategies to Enhance Liver Regeneration
Published on: May 24, 2024
Sarcopenia in Children With End-Stage Liver Disease on the Transplant Waiting List
Jessica P Woolfson1, Manuela Perez, Govind B Chavhan
1Division of Gastroenterology, Hepatology, and Nutrition the Hospital for Sick Children Toronto Ontario Canada University of Toronto Toronto Ontario Canada Department of Diagnostic Imaging and Department of Medical Imaging the Hospital for Sick Children Toronto Ontario Canada Transplant and Regenerative Medicine Centre the Hospital for Sick Children Toronto Ontario Canada.
Insights
Sarcopenia, or muscle loss, affects 40% of children with end-stage liver disease awaiting liver transplantation. This condition is linked to poorer nutritional status and longer intensive care unit stays post-transplant.
Area of Science:
- Pediatric Gastroenterology and Hepatology
- Transplantation Medicine
- Radiology and Imaging
Background:
- Sarcopenia is a known predictor of morbidity and mortality in adults with end-stage liver disease (ESLD).
- Pediatric-specific growth curves for total psoas muscle area (tPMA) now allow for sarcopenia assessment in children.
Purpose of the Study:
- To evaluate the prevalence and impact of sarcopenia in children with ESLD awaiting liver transplantation (LT).
Main Methods:
- Retrospective single-center study of children (1-16 years) with ESLD undergoing abdominal computed tomography (CT) before LT.
- Sarcopenia defined as tPMA z-score < -2 at the L4-5 level.
- Analysis of demographic, biochemical, and outcome data, including 1-year post-LT morbidity and mortality.
Main Results:
- 40% of the 25 pediatric patients studied had sarcopenia (tPMA z-score < -2).
- Sarcopenia was associated with lower weight and height z-scores and increased need for nutritional support before LT.
- Children with sarcopenia experienced longer pediatric intensive care unit (PICU) stays post-LT.
Conclusions:
- Sarcopenia is prevalent in children with ESLD awaiting LT.
- Muscle loss in these children correlates with poor anthropometrics and nutritional deficits.
- Sarcopenia is associated with adverse outcomes, including prolonged PICU stay, highlighting the need for further research into its mechanisms.
Abstract:
Sarcopenia predicts morbidity and mortality in adults with end-stage liver disease (ESLD) and is determined by total psoas muscle area (tPMA) measurement from computed tomography (CT) imaging. Recently developed pediatric age- and sex-specific tPMA growth curves provide the opportunity to ascertain prevalence and impact of sarcopenia in children awaiting liver transplantation (LT). This retrospective single-center study evaluated sarcopenia in children between 1 and 16 years with ESLD and a clinically indicated abdominal CT less than 3 months before first isolated LT. Sarcopenia was defined as tPMA z score less than -2 measured at the intervertebral L4-5 level. Patient demographic, biochemical, and outcome data were recorded. tPMA was compared with other measures of nutritional status using univariate and multivariate logistic analyses. Outcome measures included 1-year morbidity events and mortality after LT. CT images from 25 (64% female) children with median age of 5.50 (interquartile range [IQR], 3.75-11.33) years were reviewed. Ten children (40%) had a tPMA z score less than -2. Sarcopenia was associated with lower z scores for weight (odds ratio [OR], 0.38; P = 0.02), height (OR, 0.32; P = 0.03), and nutritional support before LT (OR, 12.93; P = 0.01). Sarcopenic children had a longer duration of pediatric intensive care unit (PICU) stay (3.50 [IQR, 3.00-6.00] versus 2.00 [IQR, 2.00-3.50] days; P = 0.03). Sarcopenia was prevalent in 40% of children with ESLD awaiting LT, and lower tPMA z score was associated with deficient anthropometrics and need for nutritional support before LT. Post-LT PICU duration was increased in children with sarcopenia, reflecting adverse outcomes associated with muscle loss. Further studies are needed to elucidate the underlying mechanisms of sarcopenia in children with ESLD.
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