口服骨化三醇补充维生素D时继发性甲状旁腺功能亢进血液透析患者血清白蛋白和炎症生物标志物的氧化还原状态

Q2 Pharmacology, Toxicology and Pharmaceutics
Open Medicinal Chemistry Journal Pub Date : 2018-10-18 eCollection Date: 2018-01-01 DOI:10.2174/1874104501812010098
Wesam A Nasif, Mohammed H Mukhtar, Hoda M El-Emshaty, Ahmed H Alwazna
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引用次数: 10

摘要

背景:血液透析(HD)患者继发性甲状旁腺功能亢进(s-HPT)暴露于增加的炎症和氧化应激。在HD患者中,氧化白蛋白是氧化应激的可靠标志物,其临床意义很少被研究。目的:本研究的目的是评估Cys34人血清白蛋白(HSA)作为HD合并s-HPT患者氧化应激生物标志物及其与口服骨化三醇补充维生素d时骨转换标志物炎症的关系。选取15例稳定的s-HPT血液透析患者(平均年龄48.67±8.15岁,男11例,女4例),分别给予骨化三醇治疗16周(根据患者血清钙、磷水平分别0.25mcg或0.5 mcg, 1次/ d)。分别在骨化三醇治疗前和治疗第8、16周时,检测各组血清生化指标(Ca、P、ALP、iPTH)、炎症标志物(CRP、IL-6水平)和血清氧化应激状态(SOD、IS和白蛋白比值HNA/HMA)的变化。研究了这些因素之间的相关性。结果:所有患者口服骨化三醇治疗有效,血清iPTH显著降低。结果显示骨化三醇能有效抑制iPTH分泌,血清Ca、P显著升高,ALP维持不变。还能有效降低炎症标志物(CRP、IL-6),增加氧化标志物(SOD、IS)。氧化白蛋白比(HNA/HMA)在骨化三醇治疗16周后显著(p=0.001)降低,HSA的氧化还原状态显示甲状旁腺功能亢进和炎症的阳性预测。结论:HSA的氧化还原状态可以通过延缓白蛋白氧化来预测骨化三醇治疗HD伴继发性甲状旁腺功能亢进患者的甲状旁腺功能亢进和炎症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Redox State of Human Serum Albumin and Inflammatory Biomarkers in Hemodialysis Patients with Secondary Hyperparathyroidism During Oral Calcitriol Supplementation for Vitamin D.

Redox State of Human Serum Albumin and Inflammatory Biomarkers in Hemodialysis Patients with Secondary Hyperparathyroidism During Oral Calcitriol Supplementation for Vitamin D.

Redox State of Human Serum Albumin and Inflammatory Biomarkers in Hemodialysis Patients with Secondary Hyperparathyroidism During Oral Calcitriol Supplementation for Vitamin D.

Redox State of Human Serum Albumin and Inflammatory Biomarkers in Hemodialysis Patients with Secondary Hyperparathyroidism During Oral Calcitriol Supplementation for Vitamin D.

Background: Hemodialysis (HD) patients with secondary Hyperparathyroidism (s-HPT) are exposed to increased inflammation and oxidative stress. In HD patients, oxidized albumin is a reliable marker of oxidative stress and its clinical significance has been rarely studied.

Objective: The objective of this study was to evaluate Cys34 Human Serum Albumin (HSA) as oxidative stress biomarker in HD patients with s-HPT and its relationship with inflammation on bone turnover markers during oral calcitriol supplementation for vitamin D.

Patients and methods: Fifteen stable hemodialysis patients with s-HPT (mean age 48.67±8.15, 11 males and 4 females) were used in the experiment to receive calcitriol treatment for 16 weeks (0.25mcg or 0.5 mcg once a day according to serum level of Ca and P for each). The changes in the serum biochemical parameters (Ca, P, ALP, and iPTH), inflammatory markers (CRP and IL-6 levels) and serum oxidative stress condition (SOD, IS and albumin ratio HNA/HMA) were evaluated before and at 8 and 16 weeks of calcitriol treatment. The correlations between those factors were studied.

Results: All patients responded to oral calcitriol therapy, with a significant decrease in the serum iPTH. The results showed that calcitriol could effectively suppress iPTH secretion with a significant elevation of serum Ca and P but ALP remained unchanged during the study. It can also effectively reduce the inflammatory markers (CRP and IL-6), while increasing the oxidative markers (SOD and IS). Oxidative albumin ratio HNA/HMA showed a significant (p=0.001) reduction after 16 weeks of calcitriol treatment and the redox state of HSA showed a positive prediction for hyperparathyroidism and for inflammation.

Conclusion: The redox state of HSA could be used as a predictor for monitoring hyperparathyroidism and inflammation during calcitriol treatment by retarding albumin oxidation in HD patients with secondary hyperparathyroidism.

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来源期刊
Open Medicinal Chemistry Journal
Open Medicinal Chemistry Journal Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
4.40
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