The genetics of systemic sclerosis.

被引:50
作者
Johnson R.W. [1 ]
Tew M.B. [1 ]
Arnett F.C. [1 ]
机构
[1] University of Texas Health Science Center, Department of Internal Medicine, 6431 Fannin MSB 5.260, Houston, 77030, TX
关键词
Human Leukocyte Antigen; Scleroderma; Systemic Sclerosis; Connective Tissue Growth Factor; Human Leukocyte Antigen Allele;
D O I
10.1007/s11926-002-0004-2
中图分类号
学科分类号
摘要
The etiopathogenesis of systemic sclerosis (SSc) is unclear. With no definitive evidence supporting an environmental cause, recent attention has focused on genetic factors. Familial clustering and ethnic influences have been demonstrated. Human leukocyte antigen (HLA) associations exist but are more related to the presence of particular autoantibodies rather than to the disease. In addition, no single major histocompatibility complex (MHC) allele predisposes to SSc in all ethnic groups. The role of microchimerism in SSc is a novel yet unproven hypothesis that may be related to intergenerational HLA compatibility. Recent studies investigating polymorphisms in genes coding for extracellular matrix proteins and cell-signaling molecules implicate non-MHC areas in SSc pathogenesis. The data reviewed suggest that SSc is a multigenic complex disorder.
引用
收藏
页码:99 / 107
页数:8
相关论文
共 240 条
[1]  
Mayes MD(2000)Epidemiologic studies of environmental agents and systemic autoimmune diseases Environ Health Perspect 107 743-748
[2]  
Feghali CA(1995)Epidemiologic and clinical study of twins with scleroderma [abstract] Arthritis Rheum 38 S308-S308
[3]  
Wright TM(1995)Segregation of autoantibodies with disease in monozygotic twin pairs discordant for systemic sclerosis: three further cases Arthritis Rheum 38 1845-1850
[4]  
McHugh NJ(1995)HLA and autoimmunity in scleroderma (systemic sclerosis) Int Rev Immunol 12 107-128
[5]  
Harvey GR(1996)Increased prevalence of systemic sclerosis in a Native American tribe in Oklahoma: association with an Amerindian HLA haplotype Arthritis Rheum 39 1362-1370
[6]  
Whyte J(1999)Influence of ethnic background on clinical and serologic features in patients with systemic sclerosis and anti-DNA topoisomerase I antibody Arthritis Rheum 42 465-474
[7]  
Arnett FC(1996)A tandem duplication within the fibrillin 1 gene is associated with the mouse tight skin mutation Genome Res 6 300-313
[8]  
Arnett FC(1980)Preliminary criteria for the classification of systemic sclerosis (scleroderma) Arthritis Rheum 23 581-590
[9]  
Howard RF(2000)Genetic factors in the etiology of systemic sclerosis and Raynaud phenomenon Curr Opin Rheumatol 12 511-519
[10]  
Tan FK(1996)Scleroderma epidemiology Rheum Dis Clin North Am 22 751-764