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作 者:蓝艳[1] 韦叶生[2] 唐秀生[1] 覃俊[1] 武洁[1] 覃集敏[1]
机构地区:[1]右江民族医学院附属医院皮肤科,广西省百色市533000 [2]右江民族医学院附属医院检验科,广西省百色市533000
出 处:《中华医学遗传学杂志》2008年第4期434-437,共4页Chinese Journal of Medical Genetics
基 金:广西教育厅基金资助课题(200610MS020)
摘 要:目的探讨白细胞介素-18(interleukin 18,IL-18)基因单核苷酸多态性与广西壮族系统性红斑狼疮(systematic lupus erythematosus,SLE)易感性之间的关系。方法以115例SLE患者和160名健康对照者为研究对象,应用聚合酶链反应.限制性片段长度多态性和DNA测序的方法对皿馏基因-137G/C、-607C/A单核苷酸多态性进行基因分型。结果IL-18基因-137G/C多态性在SLE组和正常人群中的分布差异无统计学意义(P〉0.05),而皿馏基因-607C/A多态性在两组人群中的分布差异有统计学意义(P〈0.05),等位基因频率的相对风险分析发现,-607C等位基因携带者患系统性红斑狼疮的风险是-607A等位基因的1.619倍(OR=1.619,95%CI:1.150~2.281)。联合基因型分析发现,IL-18的-137G/-607C等位基因频率在SLE组中显著高于对照组(P〈0.05).-137G/-607C等位基因携带者显著增加了SLE的发病风险(OR=1.484,95%CI:1.056~2.087)。结论IL-18基因-607C/A多态性与SLE的发病具有相关性,其中-607C等位基因可能是SLE的遗传易感基因。Objective To investigate the association of the single nucleotide polymorphlsms of interleukin-18 (IL-18) gene with the susceptibility to systematic lupus erythematosus (SLE) in a Chinese Zhuang population. Methods Two single nucleotide polymorphisms of the IL-18 gene promoter were analyzed, namely - 137G/C and - 607C/A, in 115 patients with SLE and 160 age and sex-matched controls in a Chinese Zhuang population, using a polymerase chain reaction-restriction fragment length polymorphism(PCR-RFLP) strategy and DNA sequencing. Restdts The IL-18 gene -607C/A polymorphism was significantly different between the SLE and control group (P 〈 0.05). The relative risk of SLE for -607C allele cartier was 1.619 times of the - 607A allele carriers (OR= 1.619,95%CI: 1. 150-2.281). Consistent with the results of the genotyping analyses, II-18 - 137G/- 607C allele frequencies in patients with SLE was significant higher than that in controls( P 〈 0.05). The - 137G/- 607C allele was associated with a significantly in- creased risk of SLE (OR = 1.484,95%CI: 1.056-2.087). However, there was no difference of the distributions of the - 137G/C polymorphism of the IL-18 gene between the SLE and control groups. Condusion IL-18 gene - 607C/A polymorphism was associated with SLE, the - 607C allele may be a risk factor for SLE.
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