The Effectiveness of Vitamin D Supplementation on Oxidative and Inflammatory Markers in Patients Suffering from End-stage Renal Disease, a Randomized Controlled Trial

被引:6
|
作者
Sharif, Dana Ahmed [1 ,2 ]
机构
[1] Univ Sulaimani, Coll Med, Dept Med, Nephrol, Kurdistan Reg, Iraq
[2] Shar Teaching Hosp, Nephrol Dept, Sulaimani, Kurdistan Reg, Iraq
关键词
Vitamin D; Inflammation; Hemodialysis; Oxidative stress; CHRONIC KIDNEY-DISEASE; CYTOKINE PRODUCTION; SERUM-ALBUMIN; ASSOCIATION; DEFICIENCY; MORTALITY; STRESS;
D O I
10.14715/cmb/2022.68.5.2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Vitamin D insufficiency is common in patients suffering from end-stage renal disease (ESRD). In contrast, vitamin D supplementation could improve the status of ESRD patients (ESRDP). However, this effect's molecular mechanism is not fully understood. Therefore, this study aimed to assess vitamin D supplementation's impact on inflammation and oxidative signaling pathways in ESRDP. 104 ESRDP were divided into placebo (53) and vitamin D (51) groups. They were also categorized into four subgroups based on the severity of vitamin D deficiency. The dose of vitamin D3 (0.25-0.5mg/day) supplementation was determined based on plasma levels of calcium and parathyroid hormone (PTH). Vitamin D supplementation was performed for eight weeks. Serum levels of calcium, phosphorus, PTH, albumin, creatinine, ALP, and glomerular filtration along with antioxidant enzymes, malondialdehyde, and pro-inflammatory factors were measured. Moreover, the Nrf2 and NF -KB expression was evaluated in whole blood. According to the results, vitamin D supplementation improved the status of patients with ESRD significantly as compared with the placebo group (p < 0.05). In addition, the expression of NF -KB and the serum levels of pro-inflammatory factors and malondialdehyde were significantly reduced. Finally, the expression of Nrf-2 and the serum of antioxidant enzymes were raised in the vitamin D group as compared with the placebo group (p < 0.05). Vitamin D reduces clinical and metabolic symptoms in ESRDP by modulating gene expression (in oxidative stress and inflammation). Copyright: (C) 2022 by the C.M.B. Association. All rights reserved.
引用
收藏
页码:7 / 15
页数:9
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