Linkage disequilibrium between HLA class II region and autoimmune hepatitis in pediatric patients

被引:56
作者
Djilali-Saiah, I
Renous, R
Caillat-Zucman, S
Debray, D
Alvarez, F
机构
[1] Hop St Justine, Div Gastroenterol, Montreal, PQ H3T 1C5, Canada
[2] Hop Necker Enfants Malad, INSERM, U25, Paris, France
[3] Hop Kremlin Bicetre, Hepatol Unit, Paris, France
关键词
autoimmune hepatitis; major histocompatibility complex genes; autoimmune regulator gene; families; transmission disequilibrium test;
D O I
10.1016/j.jhep.2004.02.023
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: Susceptibility HLA class II alleles associated with autoimmune hepatitis (AIH) were only described in case-control studies. Methods: The transmission/disequilibrium test was used in 50 simplex families with AIH, to determine if affected offspring received the disease-associated allele more frequently than its alternate. HLA-DRB1 and DQB1 allele genotyping and autoimmune regulator (AIRE) polymorphisms located in exons 6, 8 and 10 were investigated by PCR-based methods. Results: HLA-DRB1*03 allele was significantly transmitted from heterozygous parent to affected offspring (81.5%) with type I AIH compared to random expected frequency (50.0%; P = 0.004) or to unaffected offspring (42.8%; P = 0.03). HLA-DRB1*1301 allele showed. an excess transmission to affected children (100%) than expected frequency (P < 0.0001) or unaffected offspring (P = 0.001). The transmission of DQB1*201 or DQB1*0603 alleles showed significant deviation in patients compared to random frequencies: (84.8%; P < 0.0001 for DQB1*0201 or 100%; P < 0.0001 for DQB1*0603). HLA-DQB1*0201 showed a strong association with type 2 AIH in children (100.0%, P = 0.0005). Conclusions: HLA-DRB1 gene is the major genetic determinant in HLA class II region for children with type 1 AIH. Type 2 AIH is associated with the HLA-DQB1gene. Finally, AIRE gene abnormality does not contribute to the development of isolated AIH. (C) 2004 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:904 / 909
页数:6
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