Association of interleukin-1A insertion/deletion gene polymorphism and possible high risk factors with non-alcoholic fatty liver disease in Egyptian patients

Arch Physiol Biochem. 2017 Dec;123(5):330-333. doi: 10.1080/13813455.2017.1339717. Epub 2017 Jun 18.

Abstract

Context: Interleukin-1A (IL-1A) is a cytokine involved in inflammatory process. IL-1A (rs3783553) gene polymorphism is comprised in the regulation of IL-1A expression.

Objective: This study aims to evaluate association of IL-1A (I/D) gene polymorphism with NAFLD and its component traits among Egyptian populations.

Methods: The study included 75 healthy subjects and 75 patients with NAFLD. Different genotypes of IL-1A (I/D) gene polymorphism were determined by PCR-PAGE technique, serum IL-1A level and other biochemical parameters were measured.

Results: The major D allele was significantly associated with NAFLD patients (p = .002). DD genotype showed a significant increase in BMI and decrease in HDL-C. Also serum IL-1A was significantly correlated with the DD genotype. Serum IL-1A showed a significant positive correlation with BMI, triglycerides, total cholesterol, LDL-C, VLDL-C and FBG, and a significant negative correlation with HDL-C.

Conclusions: Major D allele of IL-1A (I/D) gene polymorphism is associated with NAFLD in the Egyptian population.

Keywords: IL-1A insertion/deletion gene polymorphism; non-alcoholic fatty liver disease.

MeSH terms

  • Adult
  • Case-Control Studies
  • Egypt
  • Female
  • Humans
  • INDEL Mutation*
  • Interleukin-1alpha / genetics*
  • Male
  • Middle Aged
  • Non-alcoholic Fatty Liver Disease / genetics*
  • Polymorphism, Genetic*
  • Risk Factors

Substances

  • Interleukin-1alpha