Performance of fibrosis prediction scores in paediatric non-alcoholic fatty liver disease

被引:27
作者
Jackson, Jasmine A. [1 ]
Konomi, Juna V. [2 ]
Mendoza, Michael V. [2 ]
Krasinskas, Alyssa [3 ]
Jin, Ran [2 ]
Caltharp, Shelley [3 ]
Mouzaki, Marialena [4 ]
Vos, Miriam B. [2 ]
机构
[1] Emory Univ, Sch Med, Atlanta, GA 30322 USA
[2] Emory Univ, Sch Med, Dept Paediat Gastroenterol Hepatol & Nutr, Atlanta, GA 30322 USA
[3] Emory Univ, Dept Pathol, Atlanta, GA 30322 USA
[4] Univ Toronto, Hosp Sick Children, Div Gastroenterol Hepatol & Nutr, Dept Paediat, Toronto, ON, Canada
关键词
children; fibrosis scoring system; liver enzymes; non-alcoholic fatty liver disease; non-invasive marker of hepatic fibrosis; CHILDREN; STEATOHEPATITIS; ADOLESCENTS; PREVALENCE; OVERWEIGHT; OBESITY; BIOPSY; MARKER;
D O I
10.1111/jpc.13689
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
AimNon-alcoholic fatty liver disease (NAFLD) is the leading cause of chronic liver disease in children. The phenotype of NAFLD varies widely, and non-invasive predictors of disease severity are scarce and are needed to tailor clinical management. MethodsWe compared liver fibrosis by histology with proposed non-invasive predictors of fibrosis, including alanine transaminase (ALT), aspartate transaminase (AST), AST/ALT ratio, AST to platelet ratio index, fibrosis-4, paediatric NAFLD fibrosis index and paediatric NAFLD fibrosis score. ResultsThe area under the curve of scores obtained while predicting fibrosis in children with NAFLD ranged from 0.51 to 0.67. ConclusionThe tested non-invasive fibrosis scoring systems, some of which were originally designed for adult populations, did not adequately predict fibrosis in a paediatric cohort. Further development of risk prediction scores in children are needed for the management of paediatric patients and will likely need to be developed within a large paediatric data set in order to improve specificity and sensitivity.
引用
收藏
页码:172 / 176
页数:5
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