Bader-Meunier B, Jeremiah N, Rieux-Laucat F
Service d'immunologie et rhumatologie pédiatrique, hôpital Necker, 149, rue de Sèvres, 75015 Paris, France.
Rev Med Interne. 2013 Apr;34(4):230-3. doi: 10.1016/j.revmed.2012.10.370. Epub 2012 Nov 26.
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.
系统性红斑狼疮(SLE)是由遗传和环境因素之间的复杂相互作用导致的。通常认为SLE是大量基因变异的综合作用结果,多项全基因组关联研究(GWAS)已经鉴定出大量与SLE相关的单核苷酸多态性(SNP)。然而,迄今为止所确定的基因座仅能解释SLE约15%的遗传力。最近,已经鉴定出一些狼疮的孟德尔变异,尤其是在儿童期发病的SLE中。与成人SLE患者相比,儿童患者病情更严重,女性与男性的性别比更低,遗传因素的影响更大。儿童期SLE(pSLE)的表型异质性可能与遗传异质性有关,pSLE部分可能由一系列罕见的、遗传上不同的单基因疾病组成。