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学科主题: 肾脏病学
题名:
补体B因子基因遗传多态性与IgA肾病发病和预后的关联性
其他题名: Genetic association of complement factor B gene polymorphisms with susceptibility and prognosis of IgA nephropathy
作者: 翟亚玲; 朱厉; 张宏
关键词: IgA肾病 ; B因子,补体 ; 单核苷酸多态性 ; IgA Nephropathy ; Factor B,complement ; Single nucleotide polymorphisms
刊名: 中华肾脏病杂志
发表日期: 2013
DOI: 10.3760/cma.j.issn.1001-7097.2013.07.002
卷: 29, 期:7, 页:487-492
收录类别: 中国科技核心期刊 ; 中文核心期刊 ; CSCD
文章类型: Journal Article
摘要: 目的 探讨补体B因子(CFB)基因的遗传多态性与IgA肾病发病和预后的关联性.方法 收集463例有长期随访资料的中国北方汉族IgA肾病患者和296例地域、年龄和性别匹配的健康对照人群的外周血,提取DNA后PCR法扩增基因组B因子片段,双脱氧核苷酸测序法对B因子中的4个单核苷酸多态性(SNP)位点rs4151667、rs12614、rs641153、rs 117314762进行基因分型.比较4个SNP位点的等位基因和基因型频率在IgA肾病组患者和健康对照组间的差异,分析IgA肾病患者组SNP位点与临床、病理表现以及预后的关系.结果 CFB基因中rs117314762位点的G等位基因和GG基因型频率在IgA肾病患者中显著高于健康对照组(P<0.01).CFB基因rs4151667、rs12614和rs641153位点等位基因及基因型频率在IgA肾病患者和健康对照组组间差异无统计学意义.在IgA肾病患者中,未发现CFB基因的4个SNP位点与临床、病理表现以及预后有关联关系.结论 补体B因子基因rs117314762位点与IgA肾病发病的遗传易感性相关联,提示补体B因子或其所在区段可能存在与IgA肾病发病有关联的功能变异. Objective To investigate the genetic association of complement factor B (CFB)gene polymorphisms with the susceptibility and prognosis of IgA nephropathy (IgAN).Methods Four hundreds and sixty-three Northern Han Chinese patients with IgAN and two hundreds and ninty-six geographically and ethnic matched healthy volunteers were recruited.Peripheral blood was collected from recruited individuals for DNA extracting.After amplified by plymerase chain reaction (PCR),genotyping of the four single nucleotide polymorphisms (SNPs) in CFB gene,which were rs4151667,rs12614,rs641153 and rs117314762,were performed by sequencing.Differences of allele and genotype frequencies were analyzed between IgAN patients and healthy controls.Moreover,the association between these SNPs and disease clinical manifestation,pathological features and long term renal outcome in IgAN patients were further analyzed.Results The G allele and GG genotype frequencies of rs117314762 in CFB gene were significantly higher in IgAN patients than that in healthy controls.No difference in allele and genotype frequencies of rs4151667,rs12614,rs641153 between IgAN patients and healthy controls was observed.Furthermore,no association was found between these SNPs in CFB gene and clinical manifestation,pathological features and long term renal outcome of IgAN.Conclusion Association between rs117314762 in CFB gene and IgAN susceptibility suggests that there may be functional variants in CFB gene or its linked genetic region,which needs further exploration.
语种: 中文
原文出处: 查看原文
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内容类型: 期刊论文
URI标识: http://ir.bjmu.edu.cn/handle/400002259/46099
Appears in Collections:北京大学第一临床医学院_肾脏内科_期刊论文

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作者单位: 100034,北京大学第一医院肾内科 北京大学肾脏疾病研究所 卫生部肾脏疾病重点实验室 教育部慢性肾脏病防治重点实验室(北京大学)

Recommended Citation:
翟亚玲,朱厉,张宏. 补体B因子基因遗传多态性与IgA肾病发病和预后的关联性[J]. 中华肾脏病杂志,2013,29(7):487-492.
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