Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Children's Mercy Hospital, Kansas City, Missouri, USA.
Division of Developmental and Behavioral Health, Children's Mercy Hospital, Kansas City, Missouri, USA.
Clin Transl Sci. 2022 Sep;15(9):2241-2250. doi: 10.1111/cts.13358. Epub 2022 Jul 9.
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.
肥胖和超重的儿童患非酒精性脂肪性肝病 (NAFLD) 的风险增加,这可能导致脂肪性肝炎、肝硬化和肝移植。神经精神疾病影响到越来越多的儿童,他们经常需要使用神经精神药物 (NPM),这些药物会导致体重增加和/或药物性肝损伤。我们试图评估 NPM 的长期使用在儿科 NAFLD 中的作用。对 2000 年至 2016 年间在儿童慈善医院肝脏护理中心就诊的 260 名 NAFLD 患者(NPM=77,非 NPM=183)的病历进行了回顾性研究。结果测量包括体重指数 (BMI) 百分位数、BMI z 评分、天门冬氨酸氨基转移酶 (AST)、丙氨酸氨基转移酶 (ALT)、总胆红素和谷氨酰转肽酶,这些指标在诊断时、6-18 个月随访时和 18-36 个月时进行采集。控制种族和二甲双胍的影响后,BMI z 评分(p<0.01)和总胆红素(p=0.03)随时间显著增加,而 ALT(p<0.01)和 AST(p<0.01)最初则下降。除了非 NPM 组的总胆红素较高外,未发现组间或组间交互作用有显著差异。当按 NPM 药物类别对受试者进行分析时,也观察到了类似的模式。需要进一步研究来证实这些发现,并评估 NPM 药物类别、剂量和暴露时间对儿科 NAFLD 结局的影响。