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Role of Gut-derived Uremic Toxins on Oxidative Stress and Inflammation in Patients with Chronic Kidney Disease

机译:肠源性尿毒症毒素对慢性肾脏病患者氧化应激和炎症的作用

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Several cardiovascular disease (CVD) risk factors have been identified among patients with chronic kidney disease (CKD). Gut-derived uremic toxins (GDUT) are important modifiable contributors in this respect. There are very few Indian studies on GDUT changes in CKD. One hundred and twenty patients older than 18 years diagnosed with CKD were enrolled along with forty healthy subjects. The patients were classified into three groups of forty patients based on stage of CKD. Indoxyl sulfate (IS), para cresyl sulfate (p-CS), indole acetic acid (IAA), and phenol were estimated along with the assessment of oxidative stress (OS), inflammatory state, and bone mineral disturbance. All the GDUT increased across the three groups of CKD. All patients had higher levels of malondialdehyde (MDA), ferric reducing ability of plasma (FRAP), high-sensitivity C-reactive protein (hsCRP), and interleukin-6 (IL-6) as compared to controls. IS and IAA showed positive association with MDA/FRAP corrected for uric acid, whereas IS and p-CS showed positive association with IL-6. IS, IAA, and phenol showed a positive association with calcium × phosphorus product. GDUT increase OS and inflammatory state in CKD and may contribute to CVD risk.
机译:在患有慢性肾脏疾病(CKD)的患者中已经确定了几种心血管疾病(CVD)危险因素。在这方面,肠源性尿毒症毒素(GDUT)是重要的可修饰贡献者。印度对CKD中GDUT变化的研究很少。入选了120名年龄在18岁以上的CKD患者和40名健康受试者。根据CKD的分期,将患者分为三组,每组40例。估计了吲哚硫酸盐(IS),对甲酚硫酸盐(p-CS),吲哚乙酸(IAA)和苯酚,并评估了氧化应激(OS),炎症状态和骨矿物质紊乱。三组CKD的所有GDUT均增加。与对照组相比,所有患者的丙二醛(MDA)水平,血浆铁还原能力(FRAP),高敏感性C反应蛋白(hsCRP)和白介素6(IL-6)均较高。 IS和IAA与校正了尿酸的MDA / FRAP呈正相关,而IS和p-CS与IL-6呈正相关。 IS,IAA和苯酚与钙磷产物呈正相关。 GDUT会增加CKD中的OS和炎症状态,并可能增加CVD的风险。

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