Rao A Madhusudhana, Apoorva R, Anand Usha, Anand C V, Venu G
Department of Biochemistry, PSG Institute of Medical Sciences and Research (PSGIMS&R), Coimbatore, Tamil Nadu 614004 India.
Department of Nephrology, PSG Institute of Medical Sciences and Research (PSGIMS&R), Coimbatore, Tamil Nadu 614004 India.
Indian J Clin Biochem. 2012 Jul;27(3):253-8. doi: 10.1007/s12291-012-0194-y. Epub 2012 Mar 24.
End stage renal disease (ESRD) patients on hemodialysis (HD) have an increased oxidative stress, with a high risk of atherosclerosis and other co-morbid conditions. Recent studies have suggested that myeloperoxidase (MPO)-mediated oxidative stress may play a role in the pathogenesis of cardiovascular complications in dialysis patients. Furthermore, dialysis treatment 'per se' can aggravate oxidative stress. Hence this study was designed to determine whether HD leads to an alteration in the plasma levels of MPO and malondialdehyde (MDA), a marker of oxidative stress in ESRD patients on maintenance HD. To study the effect of HD, plasma MPO and MDA were determined before and after HD in forty ESRD patients (24 men and 16 women, age between 8 and 71 years, median being 40.5 years) on maintenance HD. Plasma MPO and MDA were assayed by spectrophotometric methods. Haematological and other biochemical parameters were obtained from patients' case records. Plasma MPO and MDA levels were significantly higher after HD when compared with pre-dialysis levels (p < 0.05). There was no correlation between MPO and MDA (r = 0.184, p = 0.10) and other biochemical parameters (p > 0.05). However, there was a significant correlation between MPO and MDA with haemodialysis vintage (p < 0.05). In univariate regression analysis duration of HD (β = 1.470, p = 0.045, β = 0.388, p = 0.013), was independently associated with MPO and MDA. Although HD is indispensable for survival of patients with ESRD, it is fraught with undesirable side-effects, such as an increase in the plasma MPO and MDA levels. The elevated levels of MPO contribute to the increased oxidative stress as free radicals are produced by the reaction catalyzed by it.
接受血液透析(HD)的终末期肾病(ESRD)患者氧化应激增加,患动脉粥样硬化和其他合并症的风险很高。最近的研究表明,髓过氧化物酶(MPO)介导的氧化应激可能在透析患者心血管并发症的发病机制中起作用。此外,透析治疗本身会加重氧化应激。因此,本研究旨在确定HD是否会导致维持性HD的ESRD患者血浆中MPO和氧化应激标志物丙二醛(MDA)水平发生变化。为研究HD的影响,对40例维持性HD的ESRD患者(24例男性和16例女性,年龄在8至71岁之间,中位数为40.5岁)在HD前后测定血浆MPO和MDA。采用分光光度法测定血浆MPO和MDA。从患者病历中获取血液学和其他生化参数。与透析前水平相比,HD后血浆MPO和MDA水平显著升高(p<0.05)。MPO与MDA之间无相关性(r=0.184,p=0.10),与其他生化参数也无相关性(p>0.05)。然而,MPO和MDA与血液透析病程之间存在显著相关性(p<0.05)。在单变量回归分析中,HD持续时间(β=1.470,p=0.045,β=0.388,p=0.013)与MPO和MDA独立相关。虽然HD对ESRD患者的生存不可或缺,但它存在不良副作用,如血浆MPO和MDA水平升高。MPO水平升高会导致氧化应激增加,因为它催化的反应会产生自由基。