Seattle Children's Research Institute, Department of Pediatrics, University of Washington, Seattle, WA, USA.
Pediatr Nephrol. 2009 Dec;24(12):2309-19. doi: 10.1007/s00467-009-1199-5. Epub 2009 May 7.
Patients with moderate to advanced chronic kidney disease or end-stage renal disease have a greatly increased cardiovascular risk that cannot be explained entirely by traditional cardiovascular risk factors. An increase in oxidative stress and inflammation have been proposed as nontraditional cardiovascular risk factors in this patient population. Oxidative stress reflects the redox balance between oxidant generation and antioxidant mechanisms. The generation of reactive oxygen species is not simply a random process that oxidizes nearby macromolecules, but, in many instances, the oxidants target particular amino acid residues or lipid moieties. Oxidant mechanisms are now recognized to be intimately involved in cell signaling and to be vital components of the immune response. This is equally true for antioxidant mechanisms as well. In the progression of chronic kidney disease, the redox balance is not in equilibrium and is tipped toward oxidation, resulting in the dysregulation of cellular process and subsequent tissue injury. In this review we discuss the major oxidant and antioxidant pathways and the biomarkers to assess redox status. We also review the data linking the pathogenesis of oxidative stress, inflammation, and the progressive loss of kidney function in chronic kidney disease.
患有中重度慢性肾病或终末期肾病的患者心血管疾病风险大大增加,这不能完全用传统心血管危险因素来解释。氧化应激和炎症增加被认为是该患者人群中的非传统心血管危险因素。氧化应激反映了氧化剂生成和抗氧化机制之间的氧化还原平衡。活性氧的产生不是简单地随机氧化附近的大分子,而是在许多情况下,氧化剂针对特定的氨基酸残基或脂质部分。现在已经认识到氧化剂机制与细胞信号密切相关,并且是免疫反应的重要组成部分。抗氧化机制也是如此。在慢性肾脏病的进展中,氧化还原平衡失去平衡,向氧化倾斜,导致细胞过程失调和随后的组织损伤。在这篇综述中,我们讨论了主要的氧化剂和抗氧化途径以及评估氧化还原状态的生物标志物。我们还回顾了氧化应激、炎症和慢性肾脏病中肾功能进行性丧失的发病机制之间关联的数据。