期刊文献+

汉族寻常性银屑病患者IFN-γ受体2基因多态性研究

Polymorphism of interferon-γ receptor 2 gene in patients with psoriasis vulgaris in Chinese Hans
原文传递
导出
摘要 目的探讨IFN-γ受体2(IFN—yR2)基因氨基酸位点Gln64Arg多态性与中国汉族寻常性银屑病的相关性。方法采用PCR-限制性片段长度多态性(RFLP)方法及DNA测序方法,检测苏皖地区182例汉族寻常性银屑病患者和I14例正常人对照IFN—γR2基因Gln64Arg位点多态性。结果寻常性银屑病患者与正常人对照组IFN-γR2基因Gln64Arg多态性位点各基因型及等位基因频率分布差异无统计学意义(P〉0.05)。伴甲损害银屑病组与无甲损害银屑病组之间Gln64/Gln64基因型分布频率分别为57.5%和38.1%,差异有统计学意义(Χ^2=5.33,P=0.02);Arg64等位基因(Gln64等位基因)分布频率分别为19.3%(80.7%)和30%(70%),差异也有统计学意义(Χ^2=5.03,P=0.02)。伴甲损害的银屑病患者组Gln64/Arg64基因型分布频率为29.8%,正常人对照组为49.1%,两组间分布差异有统计学意义(Χ^2=5.48,P=0.01);Gln64/Gln64基因型分布频率在两组间分别为57.5%和35.1%,差异有统计学意义(Χ^2=6.23,P=0.01);无甲损害组与正常人对照组之间差异则无统计学意义。在以上呼吸道感染为诱因或加重因素的银屑病组与非上呼吸道感染银屑病组之间Arg64/Arg64基因型分布频率分别为33.3%和15.5%,差异有统计学意义(Χ^2=4.94,P=0.03);Arg64等位基因(Gin64等位基因)分布频率为51.9%(48.1%)和35,2%(64.8%),差异也有统计学意义(Χ^2=5.46,P=0.02)。结论IFN—γR2基因Gln64Arg多态性位点可能与寻常性银屑病患者是否伴有甲损害有关,也可能与以上呼吸道感染为诱因或加重因素的寻常性银屑病有关。 Objective To assess the association between the amino acid polymorphism (Arg64Gln) within the interferon-γ receptor 2 gene (IFN-γR2) and psoriasis vulgaris in Chinese Hans. Methods Blood samples were collected from 182 patients with psoriasis vulgaris and 114 healthy human controls in Jiangsu and Anhui provinces. The amino acid polymorphism (Arg64Gln) within the IFN-γR2 was examined by PCR-restriction fragment length polymorphism (RFLP) and DNA sequencing. Results No significant difference was observed in the amino acid polymorphism (Arg64Gln) within the IFN-γR2 between the psoriatic patients and healthy controls (P 〉 0.05 ). There was a significant difference between patients with nail involvement and those without in the frequency of Gln64/Gln64 genotype (57.5% vs 38.1%, Χ^2= 5.33, P 〈 0.05), andArg64 (Gln64) allele [19.3% (80.7%)vs30% (70%),Χ^2=5.03, P 〈 0.05 ]. The frequencies of Gln64/Arg64 genotype and Gln64/Gln64 genotype in psoriatic patients with nail involvement significantly differed from those in the controls (29.8% vs 49.1%,Χ^2 = 5.48, P 〈 0.05; 57.5% vs 35.1%, Χ^2 = 6.23, P 〈 0.05), while no significant difference was found between the psoriatic patients without nail involvement and controls. Moreover, significant difference was noted between patients with prior upper respiratory tract infec- tion (as inducements) and those without in the frequency of Arg64/Arg64 genotype (33.3% vs 15.5%,Χ^2 = 4.94, P〈 0.05) and Gln64 (Arg64) allele [51.9% (48.1%) vs 35.2% (64.8%), Χ^2 = 5.46, P〈 0.05]. Conclusion The amino acid polymorphism (Arg64Gln) within the IFN-γR2 may be associated with the nail involvement and upper respiratory tract infection in patients with psoriasis vulgaris.
出处 《中华皮肤科杂志》 CAS CSCD 北大核心 2009年第12期824-827,共4页 Chinese Journal of Dermatology
基金 江苏省“六大人才高峰”资助
关键词 银屑病 多态性 单核苷酸 受体 干扰素 Psoriasis Polymorphism, single nucleotide Receptors, interferon
  • 相关文献

参考文献7

  • 1Barker JN. Genetic aspects of psoriasis. Clin Exp Dermatol, 2001, 26(4): 321-325.
  • 2Lee MR, Cooper AJ. Immunopathogenesis of psoriasis. Australas J Dermatol, 2006, 47(3): 151-159.
  • 3Nakashima H, Inoue H, Akahoshi M, ctal. The combination of polymorphisms within interferon-gamma receptor 1 and receptor 2 associated with the risk of systemic lupus erythematosus. FEBS Lett, 1999, 453(1-2): 187-190.
  • 4Schrijver HM, Hooper-van Veen T, van Belzen MJ, et al. Polymorphisms in the genes encoding interferon-gamma and interfer- on-gamma receptors in multiple sclerosis. Eur J Immunogenet, 2004, 31(3): 133-140.
  • 5Jiaravuthisan MM, Sasseville D, Vender RB, et al. Psoriasis of the nail: anatomy, pathology, clinical presentation, and a review of the literature on therapy. J Am Aead Dermatol, 2007, 57( 1 ): 1-27.
  • 6Tham SN, Lim J J, Tay SH, et al. Clinical observations on nail changes in psoriasis. Ann Acad Med Singapore, 1988, 17 (4): 482-485.
  • 7Stuart P, Malick F, Nair RP, et al. Analysis of phenotypic variation in psoriasis as a fimction of age at onset and family history. Arch Dermatol Res, 2002, 294(5): 207-213.

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部