[Childhood-onset systemic lupus erythematosus: polygenic or monogenic disorder?]

Rev Med Interne. 2013 Apr;34(4):230-3. doi: 10.1016/j.revmed.2012.10.370. Epub 2012 Nov 26.
[Article in French]

Abstract

Systemic lupus erythematosus (SLE) results from the complex interaction between genetic and environmental factors. It is usually thought that SLE results from the combined effect of variants in a large number of genes, and several genome whole association studies (GWAS) have identified a great number of single-nucleotide polymorphisms (SNP) associated with SLE. However, the loci identified so far can account for only about 15% of the heritability of SLE. Recently, some Mendelian variants of lupus have been identified, especially in childhood-onset SLE. Children present with more severe illness, a lower sex-ratio female:male and a higher genetic contribution compared to adults with SLE. pSLE phenotype heterogeneity could be related to genetic heterogeneity, and pSLE in part might consist in a collection of rare, genetically distinct monogenic disorders.

Publication types

  • English Abstract

MeSH terms

  • Adolescent
  • Autoimmune Diseases of the Nervous System / complications
  • Autoimmune Diseases of the Nervous System / genetics
  • Child
  • Complement System Proteins / genetics
  • Genetic Predisposition to Disease
  • Humans
  • Interferon-alpha / genetics
  • Lupus Erythematosus, Systemic / genetics*
  • Mutation
  • Nervous System Malformations / complications
  • Nervous System Malformations / genetics

Substances

  • Interferon-alpha
  • Complement System Proteins

Supplementary concepts

  • Aicardi-Goutieres syndrome