Letsiou S, Nomikos T, Panagiotakos D B, Pergantis S A, Fragopoulou E, Pitsavos C, Stefanadis C, Antonopoulou S
Department of Nutrition and Dietetics, School of Health Science and Education, Harokopio University, Athens, Greece; Department of Chemistry, University of Crete, Heraklio, Crete, Greece.
Biofactors. 2014 Sep-Oct;40(5):524-35. doi: 10.1002/biof.1176. Epub 2014 Sep 4.
The epidemiology of selenium (Se) is mainly based on the determination of total serum selenium levels (TSe) which by many aspects is an inadequate marker of Se status. In this study we applied a recently developed LC-ICP-MS method, for the determination of the selenium content of the three main serum selenium-containing proteins, in a subcohort of the ATTICA study. This enables us to investigate whether the selenium distribution to selenoproteins may correlate with demographic (age, gender) and lifestyle variables (smoking, physical activity) that are crucial for the development of chronic diseases. A sub-sample from the ATTICA Study, consisted of 236 males (40 ± 11 years) and 163 females (38 ± 12 years), was selected. The selenium content of glutathione peroxidase (GPx-3), selenoprotein P (SelP) and selenoalbumin (SeAlb) was determined in serum by LC-ICP/MS method. We found that 26% of TSe is found in GPx-3, 61% in SelP and 13% in SeAlb. We have assessed the different ratios of selenoproteins' selenium content (Se-GPX-3/Se-SelP, Se-GPX-3/Se-SeAlb, Se-SelP/Se-SeAlb), showing that people with similar TSe may have different distribution of this selenium to selenoproteins. Total selenium levels and gender are the variables that mostly affect selenium distribution to selenoproteins while age, smoking, physical activity and BMI do not significantly influence selenium distribution. In conclusion, the simultaneous determination of the selenium content of serum selenium-containing selenoproteins is necessary for a thorough estimation of selenium status. The ratio of the Se content between selenoproteins may be proven a novel, valid marker of selenium status.
硒(Se)的流行病学主要基于血清总硒水平(TSe)的测定,而在许多方面,TSe并不是一个充分反映硒状态的指标。在本研究中,我们应用了一种最近开发的液相色谱 - 电感耦合等离子体质谱法(LC - ICP - MS),来测定雅典(ATTICA)研究亚队列中三种主要含硒血清蛋白的硒含量。这使我们能够研究硒在硒蛋白中的分布是否与对慢性病发展至关重要的人口统计学变量(年龄、性别)和生活方式变量(吸烟、体育活动)相关。从雅典研究中选取了一个子样本,包括236名男性(40 ± 11岁)和163名女性(38 ± 12岁)。通过LC - ICP/MS法测定血清中谷胱甘肽过氧化物酶(GPx - 3)、硒蛋白P(SelP)和硒白蛋白(SeAlb)的硒含量。我们发现,TSe的26%存在于GPx - 3中,61%存在于SelP中,13%存在于SeAlb中。我们评估了硒蛋白硒含量的不同比例(Se - GPX - 3/Se - SelP、Se - GPX - 3/Se - SeAlb、Se - SelP/Se - SeAlb),结果表明,TSe相似的人,其硒在硒蛋白中的分布可能不同。总硒水平和性别是最主要影响硒在硒蛋白中分布的变量,而年龄、吸烟、体育活动和体重指数(BMI)对硒分布没有显著影响。总之,要全面评估硒状态,同时测定含硒血清硒蛋白的硒含量是必要的。硒蛋白之间的硒含量比例可能被证明是一种新的、有效的硒状态标志物。