Gondouin Bertrand, Jourde-Chiche Noemie, Sallee Marion, Dou Laetitia, Cerini Claire, Loundou Anderson, Morange Sophie, Berland Yvon, Burtey Stephane, Brunet Philippe, Guieu Regis, Dussol Bertrand
Centre de Nephrologie et Transplantation Rx00E9;nale, Hopital La Conception, Marseille, France.
Nephron. 2015;131(3):167-74. doi: 10.1159/000441091. Epub 2015 Oct 2.
Chronic kidney disease (CKD) is associated with increased cardiovascular morbidity and mortality. Oxidative stress seems to play a pivotal role in this process, and purine metabolism may be involved in CKD-related oxidative stress. Xanthine oxidase (XO) is an enzyme involved in purine metabolism and is also responsible for the production of reactive oxygen species.
This prospective study aimed to analyze the relation between plasma dosages of molecules involved in redox balance, purine metabolism and cardiovascular events in patients with non-diabetic CKD stages 3-5 or on chronic hemodialysis (HD). CKD (n = 51) and HD (n = 50) patients were compared to matched healthy controls (n = 38) and followed-up for 3 years.
Both CKD and HD patients had decreased plasma levels of antioxidants (selenium, zinc, vitamin C). HD patients had decreased levels of the antioxidant enzyme superoxide dismutase and increased levels of oxidation products (ischemia-modified albumin, malondialdehyde [MDA]). The following substrates and enzymes involved in purine metabolism were increased in the HD cohort: adenosine, adenosine deaminase and the pro-oxidant XO. XO activity was negatively correlated with super oxide dismutase and positively with MDA. Interestingly, XO activity was an independent predictor of cardiovascular events in CKD and HD patients, regardless of uric acid levels. Uric acid was not predictive of events.
This highlights a possible role of XO itself in CKD-related cardiovascular disease (CVD) and raises the hypothesis that beneficial effects observed with XO inhibitors on CVD in CKD may also be due to the reduction of oxidative stress.
慢性肾脏病(CKD)与心血管疾病发病率和死亡率的增加相关。氧化应激似乎在这一过程中起关键作用,嘌呤代谢可能参与了与CKD相关的氧化应激。黄嘌呤氧化酶(XO)是一种参与嘌呤代谢的酶,也负责活性氧的产生。
这项前瞻性研究旨在分析非糖尿病CKD 3-5期患者或接受慢性血液透析(HD)患者体内参与氧化还原平衡、嘌呤代谢的分子血浆剂量与心血管事件之间的关系。将CKD患者(n = 51)和HD患者(n = 50)与匹配的健康对照者(n = 38)进行比较,并随访3年。
CKD患者和HD患者的血浆抗氧化剂(硒、锌、维生素C)水平均降低。HD患者的抗氧化酶超氧化物歧化酶水平降低,氧化产物(缺血修饰白蛋白、丙二醛[MDA])水平升高。HD队列中参与嘌呤代谢的以下底物和酶增加:腺苷、腺苷脱氨酶和促氧化剂XO。XO活性与超氧化物歧化酶呈负相关,与MDA呈正相关。有趣的是,无论尿酸水平如何,XO活性都是CKD和HD患者心血管事件的独立预测因子。尿酸不能预测事件。
这突出了XO本身在与CKD相关的心血管疾病(CVD)中的可能作用,并提出了一个假设,即XO抑制剂对CKD患者CVD的有益作用也可能归因于氧化应激的降低。