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糖尿病肾病中氧化应激增加及其与可溶性klotho水平的关系。

Increased oxidative stress in diabetic nephropathy and its relationship with soluble Klotho levels.

作者信息

Inci A, Olmaz R, Sarı F, Coban M, Ellidag H Y, Sarıkaya M

机构信息

Division of Nephrology, Internal Medicine, Antalya Training and Research Hospital, Antalya, Turkey.

Division of Nephrology, Internal Medicine, Akdeniz University, Faculty of Medicine, Antalya, Turkey.

出版信息

Hippokratia. 2016 Jul-Sep;20(3):198-203.

PMID:29097885
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5654436/
Abstract

BACKGROUND

In the present study, we aimed to assess the relationship between the levels of soluble Klotho (s-Klotho) and oxidative stress markers in diabetic nephropathy patients with different stages of chronic kidney disease (CKD) and albuminuria levels.

METHODS

We enrolled 109 patients with type 2 diabetes (mean age, 61.63 ± 9.77 years) and 32 healthy controls (mean age, 49.53 ± 7.32 years) between January and June 2014.  Patients were classified into three groups based on their urinary albumin/creatinine ratio (UACR). Blood samples were collected to measure the levels of s-Klotho, serum creatinine, calcium, phosphorus, 25-hydroxyvitamin D3, and parathyroid hormone (PTH). We used the total oxidant status (TOS), total antioxidant status (TAS), ischemia-modified albumin (IMA), and ischemia-modified albumin ratio (IMAR) values to measure the oxidative status. Moreover, the oxidative stress index (OSI) was estimated as the percentage ratio of TOS/TAS values.

RESULTS

The TOS, TAS, and OSI values were significantly greater in the diabetic nephropathy patients compared to controls (p <0.001). When patients were classified based on their UACR, we noted that the TOS, OSI, and IMA values did not significantly differ, although the TAS (p <0.001), and IMAR (p =0.002) values significantly differed between the groups. The s-Klotho levels also significantly differed (p =0.031) between the groups. These s-Klotho levels exhibited a significant positive correlation with TOS (r =0.186, p =0.034) and OSI (r =0.207 p =0.018), but showed no correlation with the estimated glomerular filtration rate; UACR; HbA1c, calcium, phosphorus, and PTH levels; and TAS, IMA, and IMAR values.

CONCLUSION

Oxidative stress is greater in patients with diabetic nephropathy, and the TOS was positively correlated with s-Klotho levels in diabetic patients. The therapeutic reduction of oxidative stress in patients with diabetic nephropathy could improve the renal and cardiovascular outcomes. Hippokratia 2016, 20(3): 198-203.

摘要

背景

在本研究中,我们旨在评估不同慢性肾脏病(CKD)阶段和蛋白尿水平的糖尿病肾病患者中可溶性 Klotho(s-Klotho)水平与氧化应激标志物之间的关系。

方法

2014年1月至6月,我们纳入了109例2型糖尿病患者(平均年龄61.63±9.77岁)和32例健康对照者(平均年龄49.53±7.32岁)。根据尿白蛋白/肌酐比值(UACR)将患者分为三组。采集血样以检测s-Klotho、血清肌酐、钙、磷、25-羟基维生素D3和甲状旁腺激素(PTH)水平。我们使用总氧化状态(TOS)、总抗氧化状态(TAS)、缺血修饰白蛋白(IMA)和缺血修饰白蛋白比值(IMAR)值来测量氧化状态。此外,氧化应激指数(OSI)估计为TOS/TAS值的百分比。

结果

与对照组相比,糖尿病肾病患者的TOS、TAS和OSI值显著更高(p<0.001)。当根据UACR对患者进行分类时,我们注意到TOS、OSI和IMA值无显著差异,尽管各组之间的TAS(p<0.001)和IMAR(p =0.002)值存在显著差异。各组之间的s-Klotho水平也存在显著差异(p =0.031)。这些s-Klotho水平与TOS(r =0.186,p =0.034)和OSI(r =0.207,p =0.018)呈显著正相关,但与估计的肾小球滤过率、UACR、糖化血红蛋白、钙、磷和PTH水平以及TAS、IMA和IMAR值无相关性。

结论

糖尿病肾病患者的氧化应激更大,且糖尿病患者的TOS与s-Klotho水平呈正相关。降低糖尿病肾病患者的氧化应激可能改善肾脏和心血管结局。《希波克拉底》2016年,20(3): 198 - 203。

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本文引用的文献

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J Investig Med. 2016 Aug;64(6):1128-33. doi: 10.1136/jim-2016-000142. Epub 2016 Jun 20.
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Klotho, the Holy Grail of the kidney: from salt sensitivity to chronic kidney disease.klotho,肾脏的圣杯:从盐敏感性到慢性肾脏病
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Evaluation of Ischemia-Modified Albumin, Malondialdehyde, and Advanced Oxidative Protein Products as Markers of Vascular Injury in Diabetic Nephropathy.评估缺血修饰白蛋白、丙二醛和晚期氧化蛋白产物作为糖尿病肾病血管损伤标志物的研究
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Atherosclerosis. 2014 Apr;233(2):415-418. doi: 10.1016/j.atherosclerosis.2014.01.024. Epub 2014 Jan 22.
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A decreased level of serum soluble Klotho is an independent biomarker associated with arterial stiffness in patients with chronic kidney disease.血清可溶性 Klotho 水平降低是慢性肾脏病患者动脉僵硬的独立生物标志物。
PLoS One. 2013;8(2):e56695. doi: 10.1371/journal.pone.0056695. Epub 2013 Feb 19.
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Kidney Int. 2013 Jan;83(1):121-8. doi: 10.1038/ki.2012.288. Epub 2012 Aug 15.