调节和催化抗氧化蛋白多态性在慢性肾脏疾病中的重要性

Đurđa Jerotić, M. Matić, L. McClements
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引用次数: 0

摘要

在慢性肾脏疾病(CKD)患者中发现活性氧(ROS)的过量产生和抗氧化功能受损。因此,个体对CKD的易感性可能是由编码抗氧化调节(核因子-红细胞2 -相关因子2 (Nrf2))和催化(超氧化物歧化酶(SOD2)和谷胱甘肽过氧化物酶(GPX1))蛋白的基因的功能变化引起的。在编码这些蛋白的基因中发现了几种类型的单核苷酸多态性(snp),其中Nrf2 (-617C/A), SOD2 (Ala16Val)和GPX1 (Pro198Leu)导致催化活性受损。Nrf2 (-617C/A)多态性是CKD易感性、进展和生存中最未被探索的基因多态性,仅有两项原始研究发表。这些研究的结果表明,这种多态性对终末期肾病(ESRD)发展的易感性、氧化表型和死亡率没有个体影响。然而,当与其他抗氧化基因联合使用时,Nrf2在ESRD风险和生存中发挥了重要作用。关于SOD2 (Ala16Val)和GPX1 (Pro198Leu)多态性对CKD或ESRD的影响的结果仍然没有定论。也就是说,一些研究表明,SOD2 (Val)或GPX1 (Leu)等位基因变异的患者CKD发生和进展的风险增加,而其他研究报道这些多态性与CKD之间只有微弱或没有关联。令人惊讶的是,唯一一项报道GPX1多态性与ESRD患者总体/心血管生存相关的研究显示,低活性GPX1 (Leu/Leu)基因型对更好的生存有显著影响。在这篇综述中,我们全面和批判性地评估了CKD患者中与氧化应激相关的这些多态性的文献,以找出差距并为进一步的临床研究和翻译提供建议。基于预后抗氧化基因面板,CKD患者抗氧化多态性领域的新进展可能导致CKD患者更好地分层,并为这些患者的抗氧化治疗需求提供更个性化的药物方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The importance of polymorphisms of regulatory and catalytic antioxidant proteins in chronic kidney disease
Both excessive production of reactive oxygen species (ROS) and impaired antioxidant function are found in patients with chronic kidney disease (CKD). Therefore, individual susceptibility towards CKD can be induced by functional variations of genes encoding antioxidant regulatory (nuclear factor erythroid 2 - related factor 2 (Nrf2)) and catalytic (superoxide dismutase (SOD2) and glutathione peroxidase (GPX1)) proteins. Several types of single nucleotide polymorphisms (SNPs) have been found within the genes encoding these proteins, with Nrf2 (-617C/A), SOD2 (Ala16Val) and GPX1 (Pro198Leu) conferring impaired catalytic activity. The most unexplored gene polymorphism in CKD susceptibility, progression and survival, with only two original studies published, is the Nrf2 (-617C/A) polymorphism. The results of these studies showed that there was no individual impact of this polymorphism on the susceptibility towards end stage renal disease (ESRD) development, oxidative phenotype and mortality. However, Nrf2 had a significant role in ESRD risk and survival, when combined with other antioxidant genes. The results regarding the impact of SOD2 (Ala16Val) and GPX1 (Pro198Leu) polymorphisms on either CKD or ESRD are still inconclusive. Namely, some studies showed that patients having variant SOD2 (Val) or GPX1 (Leu) allele were at increased risk of CKD development and progression, while other studies reported only weak or no association between these polymorphisms and CKD. Surprisingly, the only study that reported an association of GPX1 polymorphism with overall/cardiovascular survival in ESRD patients showed a significant impact of low activity GPX1 (Leu/Leu) genotype on better survival. In this review, we comprehensively and critically appraise the literature on these polymorphisms related to oxidative stress in CKD patients, in order to identify gaps and provide recommendations for further clinical research and translation. New developments in the field of antioxidant polymorphisms in CKD patients could lead to better stratification of CKD patients, based on a prognostic antioxidant gene panel, and provide a more personalised medicine approach for the need of antioxidant therapy in these patients.
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