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中国维持性血液透析患者中DDAH2基因-449GC和-1151AC多态性与不对称二甲基精氨酸及促红细胞生成素抵抗的关联

Association of the -449GC and -1151AC polymorphisms in the DDAH2 gene with asymmetric dimethylarginine and erythropoietin resistance in Chinese patients on maintenance hemodialysis.

作者信息

Wang Tao, Zhang Yan, Niu Kai, Wang Lijun, Shi Yanan, Liu Bing

机构信息

Department of Nephrology, Hebei General Hospital, Shijiazhuang, China.

Department of Dermatology, Hebei Provincial Tumor Hospital, Shijiazhuang, China.

出版信息

Clin Exp Pharmacol Physiol. 2017 Sep;44(9):961-964. doi: 10.1111/1440-1681.12793.

Abstract

We investigated the association of the -449G/C and -1151A/C polymorphisms in the DDAH2 gene with plasma asymmetric dimethylarginine (ADMA) concentration and erythropoietin resistance in 131 Chinese patients on maintenance hemodialysis (MHD). The -449G allele was in complete linkage disequilibrium with the -1151A allele and so were their corresponding C alleles. The -449GG/-1151AA genotype had the highest plasma ADMA concentration, erythropoietin resistance index (EPI) and serum malondialdehyde level, compared to either the -449GC/-1151AC or -449CC/-1151CC variation. The genetic effect on the ADMA and EPI was separately confirmed by multivariate regression analysis. Our findings suggested that complex genetic variations in the DDAH2 gene may influence the ADMA concentration and erythropoietin resistance in MHD patients, in which altered oxidative stress was likely involved.

摘要

我们在131例接受维持性血液透析(MHD)的中国患者中,研究了二甲基精氨酸二甲胺水解酶2(DDAH2)基因-449G/C和-1151A/C多态性与血浆不对称二甲基精氨酸(ADMA)浓度及促红细胞生成素抵抗之间的关联。-449G等位基因与-1151A等位基因完全连锁不平衡,其相应的C等位基因也是如此。与-449GC/-1151AC或-449CC/-1151CC变异相比,-449GG/-1151AA基因型的血浆ADMA浓度、促红细胞生成素抵抗指数(EPI)和血清丙二醛水平最高。通过多因素回归分析分别证实了基因对ADMA和EPI的影响。我们的研究结果表明,DDAH2基因的复杂遗传变异可能影响MHD患者的ADMA浓度和促红细胞生成素抵抗,其中氧化应激改变可能参与其中。

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