Genetic polymorphisms of the HCR gene and a genomic segment in close proximity to HLA-C are associated with patients with psoriasis in Taiwan

被引:17
作者
Chang, YT [1 ]
Shiao, YM
Chin, PJ
Liu, YL
Chou, FC
Wu, S
Lin, YF
Li, LH
Lin, MW
Liu, HN
Tsai, SF
机构
[1] Natl Yang Ming Univ, Dept Dermatol, Taipei, Taiwan
[2] Natl Yang Ming Univ, Inst Clin Med, Taipei, Taiwan
[3] Natl Yang Ming Univ, Inst Genet, Taipei, Taiwan
[4] Natl Yang Ming Univ, Fac Med, Taipei, Taiwan
[5] Taipei Vet Gen Hosp, Dept Dermatol, Taipei, Taiwan
[6] Taipei Vet Gen Hosp, Dept Med Res & Educ, Taipei, Taiwan
[7] Natl Hlth Res Inst, Div Mol & Genom Med, Taipei, Taiwan
[8] Tzu Chi Univ, Inst Med Sci, Hualien, Taiwan
关键词
Chinese; alpha-helix coiled-coil rod homologue gene; HLA-Cw*0602; psoriasis;
D O I
10.1111/j.1365-2133.2004.05972.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background Although psoriasis vulgaris (PV) is strongly associated with HLA-Cw*0602, it has been proposed that the association of Cw*0602 is due to linkage disequilibrium and that other nearby genes are involved in PV susceptibility. The alpha-helix coiled-coil rod homologue (HCR) gene, located 110 kb telomeric to the HLA-C locus, is presumed to be one of the PV candidate genes. Recently, a 10-kb genomic segment, centromeric to HLA-C, defined by two new single nucleotide polymorphisms (SNPs) n.7*A and n.9*C, was found to have a stronger association with psoriasis than the HCR gene. Until now, no study of the association of the HCR gene, SNPs n. 7, and n. 9 has been conducted on Chinese patients with psoriasis. Objectives We aimed to determine whether the genetic polymorphisms of the HCR gene, SNPs n.7*A, and n.9*C were associated with an increased risk of psoriasis in Chinese patients. Methods Using direct sequencing of the HCR gene and the genomic region containing SNPs n. 7 and n.9, we investigated the HCR gene, SNPs n.7, and n.9 for disease association in 115 Chinese patients with psoriasis and 103 control subjects. The HCR SNPs were confirmed by denaturing high performance liquid chromatography. Genotyping for HLA-Cw*0602 was also carried out using sequence-based typing. Results We observed a different allelic distribution between patient and control groups at nucleotide positions 386, 404, 1802 and 2406 of the HCR gene, and SNPs n.7, and n.9. The associations were much stronger in early onset PV patients (for HCR-386*T and HCR-404*T, odds ratio = 5.63, P-c < 0.0001). The HLA-Cw*0602 also displayed a similar association with PV (odds ratio = 5.4, P-c < 0.0001). Moreover, SNP n.7*A, SNP n.9*C, Cw*0602, HCR-386*T, HCR-404*T and HCR-1802*T were in linkage disequilibrium with each other. Haplotype-based association analysis showed SNP n.7*A-SNP n.9*C-Cw*0602-HCR-386*T-HCR-404*T-HCR-1802*T-HCR2406*G as a major susceptibility haplotype in this Chinese population (for early onset patients, odds ratio = 5.15, P-c < 0.0001). Conclusions Our results indicate that the HCR gene, SNP n.7*A, and SNP n.9*C as well as Cw*0602 are major susceptibility markers for psoriasis in Chinese patients.
引用
收藏
页码:1104 / 1111
页数:8
相关论文
共 32 条
[1]   Novel genetic association between the corneodesmosin (MHC S) gene and susceptibility to psoriasis [J].
Ahnini, RT ;
Camp, NJ ;
Cork, MJ ;
Mee, JB ;
Keohane, SG ;
Duff, GW ;
di Giovine, FS .
HUMAN MOLECULAR GENETICS, 1999, 8 (06) :1135-1140
[2]   A non-HLA gene within the MHC in psoriasis [J].
Allen, MH ;
Veal, C ;
Faassen, A ;
Powis, SH ;
Vaughan, RW ;
Trembath, RC ;
Barker, JNWN .
LANCET, 1999, 353 (9164) :1589-1590
[3]   Genetic analysis of PSORS1 distinguishes guttate psoriasis and palmoplantar pustulosis [J].
Asumalahti, K ;
Ameen, M ;
Suomela, S ;
Hagforsen, E ;
Michaëlsson, G ;
Evans, J ;
Munro, M ;
Veal, C ;
Allen, M ;
Leman, J ;
Burden, AD ;
Kirby, B ;
Connolly, M ;
Griffiths, CEM ;
Trembath, RC ;
Kere, J ;
Saarialho-Kere, U ;
Barker, JNWN .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2003, 120 (04) :627-632
[4]   Coding haplotype analysis supports HCR as the putative susceptibility gene for psoriasis at the MHC PSORS1 locus [J].
Asumalahti, K ;
Veal, C ;
Laitinen, T ;
Suomela, S ;
Allen, M ;
Elomaa, O ;
Moser, M ;
de Cid, R ;
Ripatti, S ;
Vorechovsky, I ;
Marcusson, JA ;
Nakagawa, H ;
Lazaro, C ;
Estivill, X ;
Capon, F ;
Novelli, G ;
Saarialho-Kere, U ;
Barker, J ;
Trembath, R ;
Kere, J .
HUMAN MOLECULAR GENETICS, 2002, 11 (05) :589-597
[5]   A candidate gene for psoriasis near HLA-C, HCR (Pg8), is highly polymorphic with a disease-associated susceptibility allele [J].
Asumalahti, K ;
Laitinen, T ;
Itkonen-Vatjus, R ;
Lokki, ML ;
Suomela, S ;
Snellman, E ;
Saarialho-Kere, U ;
Kere, J .
HUMAN MOLECULAR GENETICS, 2000, 9 (10) :1533-1542
[6]   Intraepidermal lymphocytes in psoriatic lesions are activated GMP-17(TIA-1)+CD8+CD3+CTLs as determined by phenotypic analysis [J].
Austin, LM ;
Coven, TR ;
Bhardwaj, N ;
Steinman, R ;
Krueger, JG .
JOURNAL OF CUTANEOUS PATHOLOGY, 1998, 25 (02) :79-88
[7]   Characterization of the major susceptibility region for psoriasis at chromosome 6p21.3 [J].
Balendran, N ;
Clough, RL ;
Arguello, JR ;
Barber, R ;
Veal, C ;
Jones, AB ;
Rosbotham, JL ;
Little, AM ;
Madrigal, A ;
Barker, JNWN ;
Powris, SH ;
Trembath, RC .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1999, 113 (03) :322-328
[8]  
Burden AD, 2000, BRIT J DERMATOL, V143, P238
[9]   Searching for the major histocompatibility complex psoriasis susceptibility gene [J].
Capon, F ;
Munro, M ;
Barker, J ;
Trembath, R .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2002, 118 (05) :745-751
[10]   A study of candidate genes for psoriasis near HLA-C in Chinese patients with psoriasis [J].
Chang, YT ;
Tsai, SF ;
Lee, DD ;
Shiao, YM ;
Huang, CY ;
Liu, HN ;
Wang, WJ ;
Wong, CK .
BRITISH JOURNAL OF DERMATOLOGY, 2003, 148 (03) :418-423