ABSTRACT
Background
Leptin plays a role in regulating energy balance, immunity, and inflammation. Studies suggest higher leptin levels might be associated with various autoimmune diseases. Most of them were in adult. To our knowledge, our study is one of the few that describe serum leptin level and leptin gene polymorphism in children with autoimmune hepatitis (AIH).
Objective
Our study aims to explore the association between serum leptin level and genetic variations in leptin gene with the likelihood of AIH in children.
Patients and methods
Thirty-one children with AIH and 29 healthy children serving as a control group were included. Serum leptin levels were measured by ELISA assays. Leptin rs2167270 genotyping was done using the real time-PCR. The relationship of serum leptin level and leptin gene polymorphism with patients’ data was studied. Patients follow up to assess treatment response.
Results
Children with AIH had significantly higher levels of leptin compared to healthy controls. GG genotype was significantly more prevalent in the AIH group compared to controls.
Conclusion
High serum leptin levels and leptin gene polymorphism may play a role in AIH development. It is worthy to recognize if leptin can serve as diagnostic and/or therapeutic target in AIH in children.
List of abbreviations
AIH | = | Autoimmune hepatitis |
BD | = | Bechet disease |
HCV | = | Hepatitis C virus |
WD | = | Wilson’s disease |
IAIHG | = | International Autoimmune Hepatitis Group |
ANA | = | Antinuclear antibody |
LKM-1 A | = | Liver-kidney microsome 1 antibody |
SMA | = | Smooth muscle antibody |
antiLC1 | = | Anti-liver cytosol type 1 antibody |
ALT | = | Alanine aminotransferase |
AST | = | Aspartate aminotransferase |
ALP | = | Alkaline phosphatase |
GGT | = | Gamma glutamyltranspeptidase |
AMA | = | Antimitochondrial antibody |
US | = | Ultrasonography |
H&E | = | Hematoxylin and eosin |
PAS | = | Periodic Acid Schiff |
WBCs | = | White blood cell count |
IFN-γ | = | Interferon gamma |
IgG | = | Immunoglobulin G |
MS | = | Multiple sclerosis |
RA | = | Rheumatoid arthritis |
SLE | = | Systemic lupus erythematosus |
T1D | = | Type 1 diabetes mellitus |
EBV | = | Epstein Barr virus |
CMV | = | Cytomegalovirus |
Acknowledgments
We would like to thank the all children and their families who participated in this study, the working staff of the departments who involved in this study in National Liver Institute and Faculty of Medicine, Menoufia University, for their sincere participation.
Disclosure statement
No potential conflict of interest was reported by the author(s).