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The effect of neuropsychiatric medication on pediatric nonalcoholic fatty liver disease
Jamie L Ryan1,2, Ashley K Sherman3, Daniel E Heble4
1Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Children's Mercy Hospital, Kansas City, Missouri, USA.
Insights
Extended use of neuropsychiatric medications (NPMs) in children with nonalcoholic fatty liver disease (NAFLD) did not significantly worsen liver enzymes or BMI z-scores over time. However, total bilirubin increased, with higher levels noted in the non-NPM group.
Area of Science:
- Pediatric Gastroenterology
- Hepatology
- Child Psychiatry
Background:
- Obesity in children increases the risk of nonalcoholic fatty liver disease (NAFLD).
- Neuropsychiatric medications (NPMs) are frequently used in children and can be associated with weight gain and liver injury.
- The impact of extended NPM use on pediatric NAFLD progression requires further investigation.
Purpose of the Study:
- To evaluate the role of extended neuropsychiatric medication (NPM) use in pediatric nonalcoholic fatty liver disease (NAFLD).
Main Methods:
- Retrospective medical chart review of 260 pediatric NAFLD patients (77 NPM, 183 non-NPM) from 2000-2016.
- Collected outcome measures: BMI percentile, BMI z-score, AST, ALT, total bilirubin, GGT at diagnosis and follow-up (6-18 and 18-36 months).
- Statistical analysis controlled for race and metformin use, examining group and time effects.
Main Results:
- Over time, significant increases were observed in BMI z-score and total bilirubin (p<0.01 and p=0.03, respectively).
- Initial decreases in ALT and AST were noted (p<0.01 for both).
- No significant main effect of NPM group or interaction effect was found on most outcomes, except for higher total bilirubin in the non-NPM group.
Conclusions:
- Extended neuropsychiatric medication (NPM) use in pediatric patients with nonalcoholic fatty liver disease (NAFLD) did not demonstrate a significant negative impact on liver enzymes or BMI z-scores over the study period.
- Further research is warranted to explore the specific effects of NPM dosage, duration, and drug class on pediatric NAFLD outcomes.
Abstract:
Obese and overweight children are at risk of developing nonalcoholic fatty liver disease (NAFLD), which can lead to steatohepatitis, cirrhosis, and liver transplantation. Neuropsychiatric conditions affect an increasing proportion of children and often require neuropsychiatric medications (NPMs) that are associated with weight gain and/or drug-induced liver injury. We sought to evaluate the role that the extended use of NPMs play in pediatric NAFLD. Medical chart review was conducted for 260 patients with NAFLD (NPM = 77, non-NPM = 183) seen in the Liver Care Center at Children's Mercy Hospital between 2000 and 2016. Outcome measures included body mass index (BMI) percentile, BMI z-score, aspartate aminotransferase (AST), alanine aminotransferase (ALT), total bilirubin, and gamma glutamyltransferase, and were collected at diagnosis, 6-18 month follow-up, and 18-36 months. Controlling for race and metformin, there was a significant increase over time in BMI z-score (p < 0.01) and total bilirubin (p = 0.03), with only initial decreases in ALT (p < 0.01) and AST (p < 0.01). Except for higher total bilirubin in the non-NPM group, no main effect of group or interaction effect was found. Similar patterns remained when subjects were analyzed by NPM drug class. Further study is needed to confirm these findings and to evaluate the effects of NPM dose and duration of exposure, by drug class, on pediatric NAFLD outcomes.
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