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作 者:陈伟强[1] 古宏标[1] 李幼姬[2] 黄玮俊[3]
机构地区:[1]广东药学院基础学院,广东广州510006 [2]中山大学附属第一医院肾脏内科,广东广州510080 [3]中山大学中山医学院医学遗传教研室,广东广州510089
出 处:《广东药学院学报》2008年第3期298-301,共4页Academic Journal of Guangdong College of Pharmacy
基 金:广东省自然科学基金(5002851);广东药学院博士启动基金项目(43543100)
摘 要:目的研究我国南方汉族IgA肾病患者Fcct R1基因5’端调控及UTR区SNPs及其单倍型与我国南方IgA肾病患者预后的关系。方法采集266例肾活检证实的IgA肾病患者血样,提取基因组DNA。用PCR产物直接测序法鉴定基因型,每3~6个月查尿蛋白、血肌酐及其他指标随访,以血肌酐浓度比基础值升高1倍以上或死亡作为随访终点。采用单因素相关分析及Logistic多元回归分析各位点多态性及其单倍型与肾功能恶化及预后的关系。结果(1)该区域单倍型对及-27、56位点多态性与肾功能进展显著相关;(2)-27位点基因型TC与TT比较差异显著(P=0.003);56位点基因型CC与TT比较,P=0.011;单倍型对TCC/CTC与TTT/TTT比较,P=0.000。结论Fcct R1基因第一外显子C56T多态位点基因型与我国南方IgAN患者预后相关。Objective To investigate the relationship between the prognoses and the polymorphisms of FcαR1 gene in Chinese Han IgA nephropathy (IgAN) patients in the South China. Methods 266 blood samples from renal-biopsies that had been proven IgA nephropathy were collected, the genotypes were determined by PCR product sequencing. All patients were followed up every 3 to 6 months by examining urinary protein, Scr, and other indicators. Follow-up was terminated when Scr value increased by one fold than the normal or in the case of the death of the patients. Follow-up lasted for more than six months. The relationship between the renal function and the polymorphisms of FcαR1 gene were evaluated by single factor analysis and multiple regression analysis with SPSS 10.0. Results ( 1 ) Haplotypes and - 27, 56 loci were significantly correlated with the aggravation of renal function. (2) Genotype TC vs. TT in - 27 locus, CC vs. TT in 56 locus, haplotypical TCC/CTC vs. TIT/TIT were different significantly on the aggravation of renal function in Chinese Han IgAN patients in the South China. Conclusion SNPs and it's haplotypes of FcαR1 gene in 5'regulatory region and UTR region were associated with the prognoses of Chinese Han IgAN patients in the South China.
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