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Single nucleotide polymorphisms in the phospholipase A2 receptor gene are associated with genetic susceptibility to idiopathic membranous nephropathy.

机译:磷脂酶A2受体基因中的单核苷酸多态性与特发性膜性肾病的遗传易感性相关。

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BACKGROUND: The phospholipase A(2) receptor (PLA2R) is a major antigen found in patients with idiopathic membranous nephropathy (MN). The relationship of genetic polymorphisms of PLA2R with the susceptibility and clinical outcomes of this disease is unknown. METHODS: We studied 199 patients with idiopathic MN followed up for 3.7 +/- 3.2 years. We enrolled 33 patients with secondary MN and 356 subjects with normal blood pressure and no proteinuria. PLA2R single nucleotide polymorphisms (SNPs) were genotyped. RESULTS: The allele frequencies of C in rs35771982 and G in rs3828323 were 73.6 and 73.9%, respectively. Subjects with the CC genotype in rs35771982 had a higher susceptibility to idiopathic MN compared to subjects with other genotypes (odds ratio 2.6; 95% confidence interval 1.8-4.0). Patients with secondary MN were not different from controls with regard to PLA2R genotype. No impact of genetic polymorphisms on renal survival was detected. CONCLUSION: The findings of this study suggest that PLA2R SNPs might be associated with the risk of developing MN.
机译:背景:磷脂酶A(2)受体(PLA2R)是特发性膜性肾病(MN)患者中发现的主要抗原。 PLA2R基因多态性与该疾病的易感性和临床结果之间的关系尚不清楚。方法:我们研究了199名特发性MN患者,随访时间为3.7 +/- 3.2年。我们招募了33例继发性MN患者和356例血压正常且无蛋白尿的患者。对PLA2R单核苷酸多态性(SNP)进行基因分型。结果:rs35771982中C的等位基因频率和rs3828323中G的等位基因频率分别为73.6%和73.9%。与其他基因型的受试者相比,rs35771982中具有CC基因型的受试者对特发性MN的敏感性更高(优势比2.6; 95%置信区间1.8-4.0)。继发性MN患者在PLA2R基因型方面与对照组无差异。没有检测到遗传多态性对肾脏存活的影响。结论:这项研究的结果表明,PLA2R SNP可能与发生MN的风险有关。

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