Ontology highlight
ABSTRACT: Background
Mitochondrial hepatopathies (MHs) are primary mitochondrial genetic disorders that can present as childhood liver disease. No recognized biomarkers discriminate MH from other childhood liver diseases. The protein biomarkers growth differentiation factor 15 (GDF15) and fibroblast growth factor 21 (FGF21) differentiate mitochondrial myopathies from other myopathies. We evaluated these biomarkers to determine if they discriminate MH from other liver diseases in children.Methods
Serum biomarkers were measured in 36 children with MH (17 had a genetic diagnosis); 38 each with biliary atresia, α1-antitrypsin deficiency, and Alagille syndrome; 20 with NASH; and 186 controls.Results
GDF15 levels compared to controls were mildly elevated in patients with α1-antitry
SUBMITTER: Van Hove JLK
PROVIDER: S-EPMC10781130 | biostudies-literature | 2024 Jan
REPOSITORIES: biostudies-literature