Childhood-onset systemic lupus erythematosus: Polygenic or monogenic disorder?

被引:7
|
作者
Bader-Meunier, B. [1 ,2 ,3 ]
Jeremiah, N. [2 ,3 ]
Rieux-Laucat, F. [2 ,3 ]
机构
[1] Hop Necker Enfants Malad, Serv Immunol & Rhumatol Pediat, F-75015 Paris, France
[2] Inserm U768, F-75015 Paris, France
[3] Fdn Imagine, F-75015 Paris, France
来源
REVUE DE MEDECINE INTERNE | 2013年 / 34卷 / 04期
关键词
Systemic lupus erythematosus; Genetics; Aicardi-Goutieres syndrome; Spondylenchondrodysplasia; Complement; Interferon-alpha; AICARDI-GOUTIERES-SYNDROME; AUTOIMMUNITY; DISEASE; DEFICIENCY; TREX1; GENE; DYSPLASIA; PHENOTYPE;
D O I
10.1016/j.revmed.2012.10.370
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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. (C) 2012 Societe nationale frangaise de medecine interne (SNFMI). Published by Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:230 / 233
页数:4
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