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首页> 外文期刊>Clinica chimica acta: International journal of clinical chemistry and applied molecular biology >Comparison of hs-cTnI, hs-cTnT, hFABP and GPBB for identifying early adverse cardiac events in patients presenting within six hours of chest pain-onset
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Comparison of hs-cTnI, hs-cTnT, hFABP and GPBB for identifying early adverse cardiac events in patients presenting within six hours of chest pain-onset

机译:hs-cTnI,hs-cTnT,hFABP和GPBB的比较,用于确定在出现胸痛六小时内出现的患者的早期不良心脏事件

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To the Editor: A recent publication comparing and assessing high-sensitivity cardiac troponin T (hs-cTnT) with heart-type fatty-acid binding protein (hFABP) at presentation in a pooled population of patients included in the FAST II (Fast Assessment of Thoracic Pain) and FASTER I (Fast Assessment of Thoracic Pain by nEuRal networks) studies indicated no incremental value for the diagnosis of myocar-dial infarction (MI) with the addition of hFABP to hs-cTnT [1]. An additional study in 3 centers in Germany on patients admitted with suspected acute coronary syndrome (ACS) to chest pain units also suggested limited utility of combining another early biomarker (glycogen phosphorylase BB; GPBB) with a sensitive cardiac troponin I (cTnI) assay for the diagnosis of acute MI [2]. However, neither of these studies assessed peak concentrations on early serial measurements (i.e., at presentation and 3 h, and 6 h later) for the diagnosis of MI as recommended by recent guidelines [3] or for predicting other short-term serious cardiac adverse events. Further work is needed here, as the pathophysiological role of GPBB, an enzyme of cellular metabolism, is believed to be released from its binding to glycogen during conditions of ischemia, which is then rapidly moved into circulation within the first hours of chest pain onset [2].
机译:致编辑:最近的出版物比较并评估了FAST II(Fast Assessment of FAST II)中合并患者的高敏感性心脏肌钙蛋白T(hs-cTnT)与心脏型脂肪酸结合蛋白(hFABP)的关系。胸痛)和FASTER I(通过nEuRal网络快速评估胸痛)的研究表明,在hs-cTnT中添加hFABP对诊断心肌梗塞(MI)没有增加的价值[1]。在德国的3个中心进行的另一项关于怀疑患有胸痛病房的急性冠状动脉综合症(ACS)入院患者的研究还表明,将另一种早期生物标志物(糖原磷酸化酶BB; GPBB)与敏感的心肌肌钙蛋白I(cTnI)检测结合使用的效用有限。急性心肌梗死的诊断[2]。然而,这些研究均未评估早期连续测量(即,在就诊时以及3 h和6 h后)的峰值浓度,以按照最新指南[3]的建议诊断MI,或预测其他短期严重心脏不良反应事件。这里需要做进一步的工作,因为GPBB(一种细胞代谢酶)的病理生理作用据信在局部缺血时会从其与糖原的结合中释放出来,然后在胸痛发作的最初几个小时内迅速进入循环[ 2]。

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