Impact of interferon-gamma and interleukin-4 gene polymorphisms on development and progression of IgA nephropathy in Japanese patients

Am J Kidney Dis. 2003 Feb;41(2):371-9. doi: 10.1053/ajkd.2003.50046.

Abstract

Background: Cytokines have an important role in the pathogenesis and disease progression of immunoglobulin A (IgA) nephropathy. The aim of this study is to investigate the impact of gene polymorphisms of T helper cell subtype 1 (T(H)1)/T(H)2 cytokines, interferon-gamma (IFN-gamma), and interleukin-4 (IL-4) on IgA nephropathy in Japanese patients.

Methods: We investigated IFN-gamma gene (IFNG) and IL-4 gene (IL4) polymorphisms in 96 patients with biopsy-confirmed IgA nephropathy who were followed-up for more than 3 years in our outpatient clinic and 61 healthy controls by polymerase chain reaction and direct sequencing methods. IFNG polymorphism was characterized as a microsatellite of intron 1. Four alleles were identified and designated IFNG 112, 114, 116, and 118, corresponding to 12, 13, 14, and 15 repeats, respectively. A variable number of tandem repeat (VNTR) polymorphisms of IL4 also were studied, and alleles were designated IL4 B1 and B2, corresponding to 2 and 3 repeats, respectively.

Results: In patients with IgA nephropathy, IFNG 114 allele and IFNG 114(+/+) genotype frequencies were significantly greater than in the healthy control group (60% versus 45%; P < 0.01 and 43% versus 23%; P < 0.05, respectively), but there was no difference between the IgA nephropathy and healthy control groups in frequencies of both IL4 VNTR allele and genotype. However, frequencies of IL4 B1 allele and B1/B1 genotype in patients with progressive IgA nephropathy (end-stage renal disease or doubling of serum creatinine level; n = 34) were significantly greater than corresponding values in the nonprogression group (n = 62; 79% versus 61%; P < 0.01 and 59% versus 34%; P < 0.05, respectively). We could not confirm an association between IgA nephropathy and polymorphisms of genes involved in the renin-angiotensin system.

Conclusion: Our results suggest that IFN-gamma and IL-4 gene polymorphisms could influence disease susceptibility and disease progression in IgA nephropathy in Japanese patients. Am J Kidney Dis 41:371-379.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Alleles
  • Creatinine / blood
  • Cytokines / genetics
  • Cytokines / physiology
  • Disease Progression
  • Female
  • Gene Frequency / genetics
  • Gene Frequency / physiology
  • Genotype
  • Glomerulonephritis, IGA / blood
  • Glomerulonephritis, IGA / genetics*
  • Glomerulonephritis, IGA / immunology*
  • Glomerulonephritis, IGA / pathology
  • Humans
  • Interferon-gamma / genetics*
  • Interferon-gamma / physiology
  • Interleukin-4 / genetics*
  • Interleukin-4 / physiology
  • Japan
  • Kidney Failure, Chronic / blood
  • Kidney Failure, Chronic / genetics
  • Male
  • Microsatellite Repeats / genetics
  • Microsatellite Repeats / physiology
  • Middle Aged
  • Polymorphism, Genetic / physiology*
  • Th1 Cells / metabolism
  • Th2 Cells / metabolism

Substances

  • Cytokines
  • Interleukin-4
  • Interferon-gamma
  • Creatinine