A new polymorphism in the GRP78 is not associated with HBV invasion

World J Gastroenterol. 2009 Oct 21;15(39):4958-61. doi: 10.3748/wjg.15.4958.

Abstract

Aim: To examine the association between -86 bp (T > A) in the glucose-regulated protein 78 gene (GRP78) and hepatitis B virus (HBV) invasion.

Methods: DNA was genotyped for the single-nucleotide polymorphism by polymerase chain reaction followed by sequencing in a sample of 382 unrelated HBV carriers and a total of 350 sex- and age-matched healthy controls. Serological markers for HBV infection were determined by enzyme-linked immunosorbent assay kits or clinical chemistry testing.

Results: The distributions of allelotype and genotype in cases were not significantly different from those in controls. In addition, our findings suggested that neither alanine aminotransferase/hepatitis B e antigen nor HBV-DNA were associated with the allele/genotype variation in HBV infected individuals.

Conclusion: -86 bp T > A polymorphism in GRP78 gene is not related to the clinical risk and acute exacerbation of HBV invasion.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Alanine Transaminase / blood
  • Asian People / genetics
  • Case-Control Studies
  • China / epidemiology
  • DNA, Viral / blood
  • Endoplasmic Reticulum Chaperone BiP
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Gene Frequency
  • Genetic Predisposition to Disease
  • Heat-Shock Proteins / genetics*
  • Hepatitis B / diagnosis
  • Hepatitis B / ethnology
  • Hepatitis B / genetics*
  • Hepatitis B Antibodies / blood
  • Hepatitis B e Antigens / blood
  • Hepatitis B virus / genetics
  • Hepatitis B virus / immunology
  • Hepatitis B virus / pathogenicity*
  • Humans
  • Logistic Models
  • Male
  • Odds Ratio
  • Phenotype
  • Polymorphism, Single Nucleotide*
  • Risk Assessment
  • Young Adult

Substances

  • DNA, Viral
  • Endoplasmic Reticulum Chaperone BiP
  • HSPA5 protein, human
  • Heat-Shock Proteins
  • Hepatitis B Antibodies
  • Hepatitis B e Antigens
  • Alanine Transaminase