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HLA and interleukin 1 gene polymorphisms in primary biliary cirrhosis: associations with disease progression and disease susceptibility
  1. P Donaldson,
  2. K Agarwal,
  3. A Craggs,
  4. W Craig,
  5. O James,
  6. D Jones
  1. Centre for Liver Research, University of Newcastle, Newcastle-upon-Tyne, UK
  1. Dr P Donaldson, Centre for Liver Research, 4th Floor William Leech Building, The Medical School, Framlington Place, Newcastle-upon-Tyne NE2 4HH, UK. p.t.donaldson{at}ncl.ac.uk

Abstract

BACKGROUND AND AIMS Twin and family studies suggest that there is a genetic component to primary biliary cirrhosis (PBC) but the genetic associations which have been described are weak with marked variations between centres. PBC is heterogeneous and genetic associations with disease progression may be obscured when the PBC population is analysed only as a whole and not subdivided.

METHODS We have investigated two candidate gene loci in 164 well characterised patients, 88 (54%) of whom had advanced disease.

RESULTS There was an increased frequency of the HLA DRB1*0801-DQA1*0401-DQB1*0402 haplotype in patients who had progressed to late stage disease (23% v 2% of controls; p=0000044; odds ratio (OR) 15.5, 95% confidence interval (CI) 3.52–68.4) but not in those with early stage disease (4%v 2%). Patients had a higher frequency of the IL-1B*1,1 genotype and lower frequencies of the IL-1B*1,2 and*2,2 genotypes (p=0.00078; OR 2.37, 95% CI 1.38–4.06), and higher frequency of theIL-1RN*1,1 genotype and lower frequency of theIL-1RN*1,2 genotype (p=0.0011; OR 2.28, 95% CI 1.34–3.89). The difference in the IL-1B*1,1genotype distribution was most marked in patients with early stage disease (77% v 43% of controls; p=0.000003; OR 4.8, 95% CI 2.31–10) but theIL-1RN genotype distribution was similar in patients with early and late stage disease.

CONCLUSIONS These data indicate a complex relationship between immunoregulatory genes and PBC. While the IL-1 genes are markers of both disease susceptibility and progression, HLA genes appear to be principally associated with disease progression.

  • human leucocyte antigens
  • primary biliary cirrhosis
  • interleukin 1
  • Abbreviations used in this paper

    HLA
    human leucocyte antigens
    PBC
    primary biliary cirrhosis
    IL
    interleukin
    IL-1RA
    interleukin 1 receptor antagonist
    PCR
    polymerase chain reaction
    OR
    odds ratio
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  • Abbreviations used in this paper

    HLA
    human leucocyte antigens
    PBC
    primary biliary cirrhosis
    IL
    interleukin
    IL-1RA
    interleukin 1 receptor antagonist
    PCR
    polymerase chain reaction
    OR
    odds ratio
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