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Genetics of liver disease: immunogenetics and disease pathogenesis
  1. P T Donaldson
  1. Correspondence to:
    Dr P T Donaldson
    Complex Genetics Research Group and Centre for Liver Research, School of Clinical Medical Sciences, The Medical School, University of Newcastle, Framlington Place, Newcastle-upon-Tyne, NE2 4HH, UK; p.t.donaldsonncl.ac.uk

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Understanding the genetic basis of “complex disease” has been heralded as one of the major challenges of the post genome era.1 However what are “complex diseases” and how will understanding the genetics of such diseases advance medical science? There has been a great deal of “hype” about the potential of the human genome mapping project.2 The three major claims are that this information will: (a) be used in diagnosis; (b) provide useful prognostic indices for disease management (including the development of individualised treatment regimens, based on the findings of both immunogenetic and pharmacogenetic studies); and (c) provide insight into the pathogenesis of these diseases. Of these three objectives the last has the greatest potential and is the least exaggerated claim. In this review I shall highlight major associations, discuss some of the practical issues that arise, and outline how current knowledge of the immunogenetic basis of chronic liver disease is beginning to inform the debate about disease pathogenesis.

AN INTRODUCTION TO COMPLEX TRAITS

Complex traits are defined as those where inheritance does not follow a Mendelian (that is, simple) pattern. This is not a new science; studies of complex traits were first performed in the mid-20th century. However, in the 21st century, the prevailing language has changed. Previously complex traits were called “polygenic” (involving more than one gene), multifactorial (depending on the interaction of the host genome and one or more environmental factors), or oligogenic (whereby individual mutations in several different genes in one or more common pathways lead to the same clinical syndrome but each patient with the disease may possess a single disease causing mutation only) (see box 1).

Box 1 Genetic diseases

Mendelian disease

  • Autosomal recessive

    • classical Mendelian pattern applies.

  • Autosomal dominant

    • classical Mendelian pattern applies.

  • Autosomal co-dominant

    • classical Mendelian pattern applies.

  • Sex linked

    • classical Mendelian pattern applies.

Complex disease …

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