Division of Nephrology and Hypertension, 1st Department of Internal Medicine, AHEPA Hospital, School of Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Clinic of Nephrology and Hypertension, Diabetes and Endocrinology, Otto von Guericke University Magdeburg, Magdeburg, Germany.
Oxid Med Cell Longev. 2017;2017:3081856. doi: 10.1155/2017/3081856. Epub 2017 Sep 12.
Hemodialysis (HD) patients are at high risk for all-cause mortality and cardiovascular events. In addition to traditional risk factors, excessive oxidative stress (OS) and chronic inflammation emerge as novel and major contributors to accelerated atherosclerosis and elevated mortality. OS is defined as the imbalance between antioxidant defense mechanisms and oxidant products, the latter overwhelming the former. OS appears in early stages of chronic kidney disease (CKD), advances along with worsening of renal failure, and is further exacerbated by the HD process per se. HD patients manifest excessive OS status due to retention of a plethora of toxins, subsidized under uremia, nutrition lacking antioxidants and turn-over of antioxidants, loss of antioxidants during renal replacement therapy, and leukocyte activation that leads to accumulation of oxidative products. Duration of dialysis therapy, iron infusion, anemia, presence of central venous catheter, and bioincompatible dialyzers are several factors triggering the development of OS. Antioxidant supplementation may take an overall protective role, even at early stages of CKD, to halt the deterioration of kidney function and antagonize systemic inflammation. Unfortunately, clinical studies have not yielded unequivocal positive outcomes when antioxidants have been administered to hemodialysis patients, likely due to their heterogeneous clinical conditions and underlying risk profile.
血液透析(HD)患者具有较高的全因死亡率和心血管事件风险。除了传统的危险因素外,过度氧化应激(OS)和慢性炎症成为加速动脉粥样硬化和死亡率升高的新的主要因素。OS 被定义为抗氧化防御机制和氧化剂产物之间的失衡,后者超过了前者。OS 出现在慢性肾脏病(CKD)的早期阶段,随着肾功能衰竭的恶化而进展,并因 HD 过程本身而进一步加剧。HD 患者由于尿毒症支持下的多种毒素潴留、缺乏抗氧化剂的营养、抗氧化剂的更替、肾脏替代治疗期间抗氧化剂的损失以及导致氧化产物积累的白细胞激活,表现出过度的 OS 状态。透析治疗的持续时间、铁输注、贫血、中央静脉导管的存在和生物不相容性透析器是触发 OS 发展的几个因素。抗氧化剂补充可能具有整体保护作用,甚至在 CKD 的早期阶段,以阻止肾功能恶化并拮抗全身炎症。不幸的是,当向血液透析患者给予抗氧化剂时,临床研究并未产生明确的阳性结果,这可能是由于他们的临床情况和潜在的风险状况存在异质性。