IL-6(-572/-597) polymorphism and expression in HBV disease chronicity in an Indian population

Am J Hum Biol. 2014 Jul-Aug;26(4):549-55. doi: 10.1002/ajhb.22562. Epub 2014 May 20.

Abstract

Objectives: This study evaluated the association among IL-6(-572) and IL-6(-597) genotypes, haplotypes, mRNA, and protein levels with hepatitis B virus (HBV)-Hepatocellular carcinoma (HCC) risk in India.

Methods: For this, 403 participants (153 controls, 61 inactive HBV-carriers, 65 chronic-active HBV patients, 63 HBV-cirrhotics, and 61 HBV-HCC participants) were enrolled in the study. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP), ELISA, and RT-PCR methods were used for assessing polymorphism, protein, and the mRNA levels, respectively, of IL-6.

Results: The study revealed that the IL-6(-572) GC genotype shared a positive association with hepatitis among controls, and a negative association with cirrhosis and consequent HCC development among carriers. However, the CC genotype shared a significant negative association with cirrhosis among controls and carriers. The IL-6(-597G>A), GA genotype acted as a potential protective factor for hepatitis, cirrhosis, and subsequent HCC development among carriers. The GA and CG haplotypes acted as a vital risk factor for HCC among controls and carriers. On the contrary, the CA haplotype was found to be a potential protective factor for HCC among carriers. Besides, the IL-6 levels significantly increased with cirrhosis development, as compared to carriers and hepatitis subjects.

Conclusions: These preliminary findings indicate a potential role of IL-6(-572/-597) genotypes in HBV disease pathogenesis in an Indian population.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carcinoma, Hepatocellular / epidemiology
  • Carcinoma, Hepatocellular / genetics
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Gene Expression Regulation
  • Genotype
  • Hepatitis B virus / physiology
  • Hepatitis B, Chronic / epidemiology
  • Hepatitis B, Chronic / genetics*
  • Humans
  • India / epidemiology
  • Interleukin-6 / genetics*
  • Interleukin-6 / metabolism
  • Liver Neoplasms / epidemiology
  • Liver Neoplasms / genetics
  • Male
  • Polymerase Chain Reaction
  • Polymorphism, Genetic*
  • Polymorphism, Restriction Fragment Length
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Risk Factors

Substances

  • IL6 protein, human
  • Interleukin-6
  • RNA, Messenger