Association between TNFA polymorphism and the development of asthma in the Japanese population

被引:58
作者
Noguchi, E
Yokouchi, Y
Shibasaki, M
Inudou, M
Nakahara, S
Nogami, T
Kamioka, M
Yamakawa-Kobayashi, K
Ichikawa, K
Matsui, A
Arinami, T
机构
[1] Univ Tsukuba, Inst Basic Med Sci, Dept Med Genet, Tsukuba, Ibaraki 3058575, Japan
[2] Univ Tsukuba, Inst Clin Med, Dept Pediat, Tsukuba, Ibaraki 3058575, Japan
[3] Nogami Childrens Clin, Ibaraki, Japan
关键词
genetics; haplotype; transmission disequilibrium test;
D O I
10.1164/rccm.2110052
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Tumor necrosis factor (TNF) is a proinflammatory cytokine that participates in the inflammatory reaction in patients with asthma. The TNFA and TNFB genes, which encode TNF-alpha and TNF-beta, respectively, are located within the region encoding the human major histocompatibility complex on chromosome 6p21.3, which showed linkage to atopic asthma in our genome-wide search. To determine whether polymorphisms in the 5' flanking region of the TNFA gene (-1031C/T, -863C/A, and -857C/T) and an Ncol polymorphism in the TNFB gene (LTA Ncol) are associated with the development of asthma, we performed transmission disequilibrium tests of families identified through children with atopic asthma. Genotypes of families were determined by polymerase chain reaction-based restriction fragment length polymorphism or SNaPshot analysis. Transmission disequilibrium tests of 144 asthmatic families revealed that transmission of the -857C allele and the -1031T-863C-857C haplotype in the TNFA gene to asthma-affected offspring occurred more frequently than expected (-857C allele, p = 0.0055; -1031T-863C-857C haplotype, p = 0.0002). Our results suggest that TNFA or nearby genes, including those in the major histocompatibility complex region, may contribute to the development of asthma in the Japanese population.
引用
收藏
页码:43 / 46
页数:4
相关论文
共 29 条
[1]   GOLD - Graphical Overview of Linkage Disequilibrium [J].
Abecasis, GR ;
Cookson, WOC .
BIOINFORMATICS, 2000, 16 (02) :182-183
[2]  
Albuquerque RV, 1998, CLIN EXP ALLERGY, V28, P578
[3]   Antibodies to tumour necrosis factor α as treatment for Crohn's disease [J].
Bell, S ;
Kamm, MA .
LANCET, 2000, 355 (9207) :858-860
[4]   Prevalence of tumor necrosis factor-α and angiotensin converting enzyme polymorphisms in mild moderate and fatal/near-fatal asthma [J].
Chagani, T ;
Paré, PD ;
Zhu, S ;
Weir, TD ;
Bai, TR ;
Behbehani, NA ;
Fitzgerald, JM ;
Sandford, AJ .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1999, 160 (01) :278-282
[5]  
Cunningham S.J., 1997, EMERG PEDIAT, V10, P33
[6]   Advances in immunology - Autoimmune diseases [J].
Davidson, A ;
Diamond, B .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (05) :340-350
[7]   Polymorphism of the 5′-flanking region of the human tumor necrosis factor (TNF)-α gene in Japanese [J].
Higuchi, T ;
Seki, N ;
Kamizono, S ;
Yamada, A ;
Kimura, A ;
Kato, H ;
Itoh, K .
TISSUE ANTIGENS, 1998, 51 (06) :605-612
[8]  
Kruglyak L, 1996, AM J HUM GENET, V58, P1347
[9]   Lack of association between adult asthma and the tumour necrosis factor α-308 polymorphism gene [J].
Louis, R ;
Leyder, E ;
Malaise, M ;
Bartsch, P ;
Louis, E .
EUROPEAN RESPIRATORY JOURNAL, 2000, 16 (04) :604-608
[10]   Anti-cytokine therapy for rheumatoid arthritis [J].
Maini, RN ;
Taylor, PC .
ANNUAL REVIEW OF MEDICINE, 2000, 51 :207-229