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Published on: April 28, 2020
Persistent alanine aminotransferase elevations in children with parenteral nutrition-associated liver disease
Chi-Fu Jeffrey Yang1, Michele Lee, Clarissa Valim
1Harvard Medical School, Boston, MA 02115, USA.
Insights
Children with parenteral nutrition-associated liver disease (PNALD) often have persistent elevated alanine aminotransferase (ALT) levels, indicating ongoing liver injury even after direct bilirubin normalizes and they achieve enteral nutrition independence.
Area of Science:
- Pediatric Gastroenterology
- Hepatology
- Clinical Nutrition
Background:
- Parenteral nutrition-associated liver disease (PNALD) is a significant complication in children with short bowel syndrome.
- Early identification and monitoring of liver injury are crucial for managing PNALD.
Purpose of the Study:
- To longitudinally assess serum alanine aminotransferase (ALT) levels in children with PNALD who are transitioning to enteral nutrition.
- To evaluate the correlation between ALT normalization and direct bilirubin levels in this cohort.
Main Methods:
- Retrospective chart review of 31 pediatric patients with PNALD.
- Analysis of patients who achieved full enteral nutrition tolerance after a minimum of 3 months of parenteral nutrition.
- Kaplan-Meier and Cox proportional hazards methods were used to estimate time to normalization of ALT and direct bilirubin.
Main Results:
- After transitioning to enteral nutrition, 74% of children normalized direct bilirubin, while only 50% normalized ALT.
- Median time to direct bilirubin normalization was 13 weeks, compared to 35 weeks for ALT normalization (P = .001).
- Persistent ALT elevation was observed in children with PNALD despite normalization of direct bilirubin.
Conclusions:
- Children achieving enteral nutrition independence with PNALD may experience ongoing hepatic injury, as indicated by persistent ALT elevation.
- ALT normalization lags behind direct bilirubin normalization, suggesting a prolonged recovery period for liver function.
- This study highlights the importance of monitoring ALT beyond bilirubin levels in children recovering from PNALD.
Background:
Parenteral nutrition-associated liver disease (PNALD) is a serious condition affecting many children with short bowel syndrome. The aim of this study was to longitudinally assess serum alanine aminotransferase (ALT), a marker for hepatocyte injury, in enterally fed children with PNALD.
Methods:
Retrospective chart review of 31 patients treated from 1999 to 2006 by the Center for Advanced Intestinal Rehabilitation at Children's Hospital Boston (Mass). Inclusion criteria included PN duration of greater than 3 months with subsequent tolerance of full enteral nutrition and evidence of PN-associated liver injury. Time to normalize ALT and direct bilirubin were estimated using Kaplan-Meier and Cox proportional hazards methods.
Results:
Mean age PN cessation was 6 months (range, 2-14 months). Median PN duration was 18 weeks (interquartile range [IQR], 13-33 weeks), and median follow-up was 24 weeks (IQR, 14-48 weeks). After transition to full enteral nutrition, 74% of children normalized direct bilirubin, whereas only 50% normalized ALT. Kaplan-Meier median time to direct bilirubin and ALT normalization were 13 weeks and 35 weeks, respectively (P = .001).
Conclusion:
Children with PNALD who have achieved PN independence have persistent ALT elevation despite normal direct bilirubin levels. This implies that hepatic injury may be ongoing beyond the time of bilirubin normalization in this cohort of patients.
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