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Psoriasis vulgaris in Chinese individuals is associated with PSORS1C3 and CDSN genes
被引:30
作者:
Chang, Y. T.
[1
]
Chou, C. T.
Shiao, Y. M.
Lin, M. W.
Yu, C. W.
Chen, C. C.
Huang, C. H.
Lee, D. D.
Liu, H. N.
Wang, W. J.
Tsai, S. F.
机构:
[1] Natl Yang Ming Univ, Dept Dermatol, Taipei 112, Taiwan
[2] Natl Yang Ming Univ, Fac Life Sci, Taipei 112, Taiwan
[3] Natl Yang Ming Univ, Inst Genome Sci, Taipei 112, Taiwan
[4] Natl Yang Ming Univ, Fac Med, Taipei 112, Taiwan
[5] Taipei Vet Gen Hosp, Dept Dermatol, Taipei 11217, Taiwan
[6] Taipei Vet Gen Hosp, Div Allergy Immunol Rheumatol, Taipei 11217, Taiwan
[7] Taipei Vet Gen Hosp, Dept Med Res & Educ, Taipei 11217, Taiwan
[8] Natl Def Med Ctr, Dept Dermatol, Taipei, Taiwan
[9] Natl Hlth Res Inst, Div Mol & Genom Med, Taipei, Taiwan
关键词:
alpha-helix coiled-coil rod homologue gene;
Chinese;
corneodesmosin gene;
HLA-Cw*0602;
psoriasis susceptibility 1 candidate 3 gene;
psoriasis vulgaris;
D O I:
10.1111/j.1365-2133.2006.07420.x
中图分类号:
R75 [皮肤病学与性病学];
学科分类号:
100206 ;
摘要:
Background Besides the HLA-Cw*0602 allele, the psoriasis susceptibility 1 candidate 3 (PSORS1C3) and corneodesmosin (CDSN) genes are two probable psoriasis susceptibility genes in the PSORS1 locus. The -79C, -26C and +246A alleles of the PSORS1C3 gene, the CDSN*971T allele, CDSN*TTC (619T-1236T-1243C) and CDSN*5 (619T-1240G-1243C) are strongly associated with psoriasis in the caucasian population. Until now, no haplotype study of the PSORS1C3 and CDSN genes has been documented in Chinese patients with psoriasis vulgaris. Objectives We aimed to determine whether genetic polymorphisms of the PSORS1C3 and CDSN genes were associated with an increased risk of psoriasis vulgaris in Chinese patients in Taiwan. Methods We investigated the PSORS1C3 and CDSN genes for disease association by direct sequencing in 178 patients with psoriasis vulgaris and 203 control subjects. Genotyping for HLA-Cw*0602, alpha-helix coiled-coil rod homologue (HCR) gene and single nucleotide polymorphism (SNP) n.9 was also carried out using a sequence-based typing method. Results The PSORS1C3*582A allele, an SNP in the 3'-untranslated region of the PSORS1C3 gene, was a major psoriasis vulgaris susceptibility allele in the Chinese population, and the association was much stronger in patients with early-onset psoriasis vulgaris (22.3% vs. 6.9%, odds ratio 3 87, P-c = 0.0000072). The frequencies of CDSN*TTC and CDSN*971T were also significantly increased in patients with early-onset psoriasis vulgaris. Moreover, PSORS1C3*582A, SNP n.9*C, Cw*0602 and HCR*WWCC were in near complete linkage disequilibrium (LD) with each other; in contrast, the LD with the CDSN gene was not so strong. SNP n.9*C-Cw*0602-PSORS1C3*582A-HCR*WWCC was a major susceptibility haplotype in patients with early-onset psoriasis vulgaris (P < 10(-7)) and this risk haplotype also carried CDSN*TTC and CDSN*971T. Conclusions The PSORS1C3 and CDSN genes are important psoriasis susceptibility genes in Chinese patients with psoriasis vulgaris.
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页码:663 / 669
页数:7
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