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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:5
|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.
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页码:7 / 15
页数:9
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