Institut für Experimentelle Endokrinologie, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, D-13353 Berlin, Germany.
Cardiovascular Critical Care & Anesthesia Research and Evaluation (3CARE), RWTH-Aachen University, D-52074 Aachen, Germany.
Nutrients. 2019 Aug 25;11(9):2005. doi: 10.3390/nu11092005.
Selenium-binding protein 1 (SELENBP1) is an intracellular protein that has been detected in the circulation in response to myocardial infarction. Hypoxia and cardiac surgery affect selenoprotein expression and selenium (Se) status. For this reason, we decided to analyze circulating SELENBP1 concentrations in patients ( = 75) necessitating cardioplegia and a cardiopulmonary bypass (CPB) during the course of the cardiac surgery. Serum samples were collected at seven time-points spanning the full surgical process. SELENBP1 was quantified by a highly sensitive newly developed immunological assay. Serum concentrations of SELENBP1 increased markedly during the intervention and showed a positive association with the duration of ischemia (ρ = 0.6, < 0.0001). Elevated serum SELENBP1 concentrations at 1 h after arrival at the intensive care unit (post-surgery) were predictive to identify patients at risk of adverse outcome (death, bradycardia or cerebral ischemia, "endpoint 1"; OR 29.9, CI 3.3-268.8, = 0.00027). Circulating SELENBP1 during intervention (2 min after reperfusion or 15 min after weaning from the CPB) correlated positively with an established marker of myocardial infarction (CK-MB) measured after the intervention (each with ρ = 0.5, < 0.0001). We concluded that serum concentrations of SELENBP1 were strongly associated with cardiac arrest and the duration of myocardial ischemia already early during surgery, thereby constituting a novel and promising quantitative marker for myocardial hypoxia, with a high potential to improve diagnostics and prediction in combination with the established clinical parameters.
硒结合蛋白 1(SELENBP1)是一种细胞内蛋白,在心肌梗死后会在血液中被检测到。缺氧和心脏手术会影响硒蛋白的表达和硒(Se)状态。出于这个原因,我们决定分析需要心脏停搏和体外循环(CPB)的心脏手术患者(= 75)的循环 SELENBP1 浓度。在整个手术过程中,在七个时间点采集血清样本。通过新开发的高度敏感的免疫测定法定量 SELENBP1。SELENBP1 血清浓度在干预过程中显着增加,并与缺血持续时间呈正相关(ρ= 0.6,<0.0001)。到达重症监护病房后 1 小时(手术后)升高的血清 SELENBP1 浓度可预测识别发生不良结局(死亡、心动过缓或脑缺血,“终点 1”)的风险患者(OR 29.9,CI 3.3-268.8,= 0.00027)。干预期间的循环 SELENBP1(再灌注后 2 分钟或从 CPB 脱机后 15 分钟)与干预后测量的心肌梗死的既定标志物(CK-MB)呈正相关(每个ρ= 0.5,<0.0001)。我们得出结论,SELENBP1 血清浓度与心脏骤停和心肌缺血的持续时间密切相关,这在手术早期就已经发生,因此构成了一种新的有前途的定量标志物,用于检测心肌缺氧,与既定的临床参数相结合,具有很高的诊断和预测潜力。