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作 者:韩媛[1] 黄松明[1] 张爱华[1] 张维真[1] 朱春华[1]
机构地区:[1]南京医科大学附属南京儿童医院肾脏科,江苏南京210008
出 处:《南京医科大学学报(自然科学版)》2010年第9期1301-1305,共5页Journal of Nanjing Medical University(Natural Sciences)
基 金:江苏省卫生厅科技基金(H200747);南京市医学重点发展项目(ZKX08007);南京医科大学校基金(07NMUM085)
摘 要:目的:探讨补体C4基因多态性与中国汉族儿童紫癜性肾炎(Henoch-Schonlein nephritis,HSPN)的关系。方法:应用聚和酶链反应技术对74例紫癜性肾炎(HSPN)和114例单纯过敏性紫癜(Henoch-Schonlein purpura,HSP)汉族儿童进行补体C4基因型分析。130例性别、年龄匹配的健康汉族儿童作为对照组。分析紫癜性肾炎(HSPN)临床表现、病理改变、疗效、血补体C4水平与其基因多态性的关系。结果:HSP患儿(包括HSPN)C4AQ0频率高于健康对照组(7.98%,0.77%,P<0.01,OR=11.19,95%CI为1.45~85.76)。HSPN组和单纯HSP组C4AQ0频率无统计学差异(7.89%,8.11%,P>0.95)。HSPN患儿C4AQ0组血清补体C4水平(0.22±0.03g/L)低于无C4AQ0组(0.26±0.05g/L),有显著性差异(P<0.05)。HSPN患儿C4AQ0组与无C4AQ0组临床表现、病理类型及疗效无显著性差异(P>0.05)。结论:补体C4基因多态性与汉族儿童HSP易感性有关,与HSPN易感性及临床表现、病理类型及疗效无关。Objective:To study the relationship of complement C4 gene polymorphism in children with Henoch-Schonlein nepritis.Methods:Total of 74 ethnic Han children with HSPN and 114 only with HSP,were enrolled,and 130 age-,sex-and ethnic-matched healthy children were used as the control group.complement C4 gene polymorphism were determined by PCR.The correlations between complement C4 gene polymorphism and clinical presentation,pathlogical changes,therapy effect were analyzed.Results:The frequencies of C4AQ0 in HSP(including HSPN)were significantly higher than those in the control group(7.98% vs.0.77%,P 〈 0.01,OR=11.19,95%CI:1.45~85.76).The frequencies of C4AQ0 in HSPN did not differ from those in children without nephritis(7.89% vs.8.11%,P 〉 0.95).Plasma complement C4 levels in HSPN with C4AQ0(0.22±0.03 g /L)were significantly lower than those without C4AQ0(0.26±0.05 g /L)(P 〈 0.05).There were no significant difference between C4AQ0 and clinical presentation,pathlogical changes,therapy effect of children with HSPN.Conclusion:Complement C4 gene polymorphism may be associated with the development of HSP and seems unrelated to the susceptibility and clinical presentation,pathlogical changes,therapy effect to HSPN.
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