Prognostic molecular markers in pediatric liver disease - Are there any?
Jon Nielsen1, Vibeke Brix Christensen1, Lise Borgwardt2
1Department of Paediatrics and Adolescent Medicine, Copenhagen University Hospital Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen Ø, Denmark.
Insights
Identifying prognostic molecular markers for pediatric liver disease (PLD) is challenging due to limited data. Further research is needed to understand PLD mechanisms and find reliable biomarkers for better patient outcomes.
Area of Science:
- Hepatology
- Pediatric Gastroenterology
- Molecular Biology
Background:
- Pediatric liver disease (PLD) causes significant morbidity and hospitalization in children.
- Prognostic stratification of pediatric patients with liver disease is difficult.
- Limited understanding of molecular mechanisms hinders the discovery of reliable prognostic biomarkers for PLD.
Purpose of the Study:
- To systematically review molecular markers with prognostic potential in pediatric liver disease.
- To identify markers related to survival, liver transplantation (LT), and disease progression/regression.
- To assess the current evidence level and identify research gaps in PLD biomarker discovery.
Main Methods:
- Systematic literature search of MEDLINE (PubMed) and Embase (OVID) from August 2007 to August 2017.
- Selection of studies reporting molecular markers with prognostic relevance in PLD.
- Inclusion of studies focusing on biliary atresia, non-alcoholic fatty liver disease, viral hepatitis, and LT.
Main Results:
- Included 23 studies with 898 patients, predominantly small, single-center studies with high bias risk.
- Identified markers related to morphogenesis, fibrosis, metabolic pathways, and inflammation.
- Found limited evidence, highlighting the need for further validation of molecular markers in PLD.
Conclusions:
- Current evidence for molecular prognostic biomarkers in pediatric liver disease is limited and of low quality.
- Further robust biological and clinical studies are essential to advance molecular insights into PLD.
- Improved understanding of molecular mechanisms is crucial for developing reliable prognostic tools and improving pediatric liver disease management.
Abstract:
Pediatric liver disease (PLD) is a major cause of severe morbidity and prolonged hospitalizations in children. Stratifying patients in terms of prognosis remains challenging. The limited knowledge about molecular mechanisms causing and accompanying PLD remains the main obstacle in a search for reliable prognostic biomarkers. A systematic search of MEDLINE via PubMed and Embase via OVID was conducted on studies published between August 2007 and August 2017. Molecular markers with a prognostic potential in terms of survival, need for liver transplantation or disease progression/regression were selected. In general, identified studies were single center smaller case-control studies or case series with a low level of evidence and a high risk of bias. Only 23 studies comprising 898 patients could be included, mostly focusing on biliary atresia, non-alcoholic fatty liver disease, viral hepatitis, and LT; and markers related to morphogenesis and fibrosis. Furthermore, molecular markers in metabolic pathways and inflammation shown to be relevant, however requiring further validation. Hence, further biological and clinical studies are needed to gain greater molecular insight into PLD.
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