Assessment of ghrelin serum level and gene polymorphism as a risk factor in progression of chronic viral hepatitis
Lamiaa Mahmoud Kamel, Nagwa Mohamed Shawky, Amal A Jouda, Amany Mohamed Ibrahim, Heba H. Mahboub, Sherif Y. Mohammed

TL;DR
This study explores whether ghrelin gene polymorphisms and serum levels are linked to the progression of chronic viral hepatitis to liver disease in Egyptian patients.
Contribution
This is the first study to evaluate ghrelin gene polymorphism as a risk factor for liver disease progression in Egyptian patients.
Findings
All groups had the GG rs34911341 genotype, with no link to disease progression.
The CA genotype of rs696217 was more common in healthy controls than in cirrhotic and HCC patients.
Serum ghrelin levels were significantly lower in liver disease patients compared to controls.
Abstract
Hepatocellular carcinoma (HCC) is a significant health concern, ranking as the fourth most common cancer in Egypt and the sixth globally. Research has identified over 300 single nucleotide polymorphisms (SNPs) in the ghrelin gene, with four of these SNPs being associated with pathogenicity. The current work is a pioneer attempt to evaluate the role of Ghrelin gene polymorphism as a risk factor for progression of chronic viral hepatitis to cirrhosis and hepatocellular carcinoma in Egyptian patients. This study was carried out on 80 cases and were allocated into four groups: Group I: apparently healthy individuals, Group II: patients with chronic viral hepatitis, Group III: patients with post-hepatitic cirrhosis, and Group IV: patients with viral hepatitis-related HCC. Serum Ghrelin was measured by ELISA Kit. Molecular detection of Ghrelin rs34911341 and rs696217 were assessed using DNA…
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Taxonomy
TopicsRegulation of Appetite and Obesity · Adipose Tissue and Metabolism · Adipokines, Inflammation, and Metabolic Diseases
