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老年人循环谷胱甘肽过氧化物酶-3与肾功能、心血管死亡率以及硒和辅酶Q补充剂的影响

Circulating Glutathione Peroxidase-3 in Elderly-Association with Renal Function, Cardiovascular Mortality, and Impact of Selenium and Coenzyme Q Supplementation.

作者信息

Alexander Jan, Aaseth Jan Olav, Schomburg Lutz, Chillon Thilo Samson, Larsson Anders, Alehagen Urban

机构信息

Norwegian Institute of Public Health, N-0213 Oslo, Norway.

Research Department, Innlandet Hospital Trust, N-2381 Brumunddal, Norway.

出版信息

Antioxidants (Basel). 2024 Dec 19;13(12):1566. doi: 10.3390/antiox13121566.

DOI:10.3390/antiox13121566
PMID:39765894
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11672870/
Abstract

Low-selenium status was associated with impaired renal function, which improved after selenium and coenzyme Q supplementation in an RCT. Here, we evaluated serum glutathione peroxidase-3 (GPx3) and its relation to serum selenium, selenoprotein P (SELENOP), renal function, mortality, and the impact of supplementation, which are all important, especially in elderly individuals. In total, 383 study participants (197 receiving selenium yeast and coenzyme Q and 186 on a placebo) were evaluated. We applied benchmark dose modelling to determine GPx3 saturation, ANCOVA, Kaplan-Meier, and multivariate Cox proportional regression analyses for mortality evaluations. Selenium and GPx3 activity were modestly correlated. In comparison with SELENOP, GPx3 levelled off at a much lower value, 100 vs. 150 µg Se/L. GPx3 was associated with renal function, but not SELENOP. Supplementation increased glomerular function by ≈23% with an increase in GPx3. Being low in GPx3 displayed twice the risks of mortality in both placebos and active treatments. At serum selenium <100 µg/L, GPx3 activity was dependent on both selenium status and renal function. As renal function is reduced in the elderly, GPx3 is not an appropriate marker of selenium status. Low GPx3 was associated with an increased risk of mortality dependent of selenium status and independent of renal function.

摘要

低硒状态与肾功能受损有关,在一项随机对照试验中,补充硒和辅酶Q后肾功能得到改善。在此,我们评估了血清谷胱甘肽过氧化物酶-3(GPx3)及其与血清硒、硒蛋白P(SELENOP)、肾功能、死亡率以及补充剂影响的关系,这些都很重要,尤其是在老年人中。总共评估了383名研究参与者(197名接受硒酵母和辅酶Q,186名接受安慰剂)。我们应用基准剂量模型来确定GPx3饱和度,采用协方差分析、Kaplan-Meier分析和多变量Cox比例回归分析进行死亡率评估。硒与GPx3活性呈适度相关。与SELENOP相比,GPx3在低得多的值时趋于平稳,分别为100和150μg Se/L。GPx3与肾功能相关,但与SELENOP无关。补充剂使肾小球功能增加约23%,同时GPx3增加。GPx3水平低在安慰剂组和活性治疗组中死亡风险均增加两倍。在血清硒<100μg/L时,GPx3活性取决于硒状态和肾功能。由于老年人肾功能下降,GPx3不是硒状态的合适标志物。低GPx3与死亡风险增加有关,这取决于硒状态且与肾功能无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fa0/11672870/663389466a71/antioxidants-13-01566-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fa0/11672870/00c5f78afca6/antioxidants-13-01566-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fa0/11672870/f42f27ef56bd/antioxidants-13-01566-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fa0/11672870/f29d84b168ad/antioxidants-13-01566-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fa0/11672870/63d2362b434f/antioxidants-13-01566-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fa0/11672870/663389466a71/antioxidants-13-01566-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fa0/11672870/00c5f78afca6/antioxidants-13-01566-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fa0/11672870/f42f27ef56bd/antioxidants-13-01566-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fa0/11672870/f29d84b168ad/antioxidants-13-01566-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fa0/11672870/63d2362b434f/antioxidants-13-01566-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fa0/11672870/663389466a71/antioxidants-13-01566-g005.jpg

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