Lacnák B, Stejskal D, Jedelský L, Karpísek M, Sprongl L
Interní oddelení nemocnice Sternberk.
Vnitr Lek. 2007 Nov;53(11):1164-9.
Glykogen Phosphorylase BB is considered a timely and specific marker of acute coronary syndrome. A kit for measuring Glykogen Phosphorylase BB in routine diagnosis has been released recently.
To test the utilisation of Glykogen Phosphorylase BB measurement in the diagnosis of acute coronary syndrome.
70 patients with suspected acute coronary syndrome were tested. A final diagnosis of acute coronary syndrome/non-coronary difficulties was made according to ESC/ACC/AHA criteria. Measurements of troponin I, myoglobin and GPBB in venous plasma (heparin-lithium) were taken for all probands on admission and two and six hours later.
Individuals with acute coronary syndrome (n = 52) had significantly higher levels of Glykogen Phosphorylase BB on admission and 2 hours after admission (21.9 vs 6.2; 18.7 vs 5.9 microg/l; p < 0.01). Levels of Glykogen Phosphorylase BB had a greater diagnostic effectiveness for the presence of acute coronary syndrome than levels of troponin I (threshold below ROC curve 0.89 vs. 0.78; 0.87 vs. 0.67). In the first two hours after admission, only levels of Glykogen Phosphorylase BB were included as independent variables in the regression model for the incidence of acute coronary syndrome (p < 0.05). When the group of patients with myocardial necrosis (n = 39; acute myocardial infarction without ST elevations on ECG; NSTEMI) is removed from the group with acute coronary syndrome, it was found that only GPBB and cTnl were independent variables in the regression model on initial testing and after two hours. After adjusting GPBB to cTnl, significantly higher levels of GPBB adjusted to troponin I were found in persons with NSTEMI (14.5 vs -48.0; p < 0.01).
Measurement of Glykogen Phosphorylase BB has excellent effectiveness independently of troponin in the first hours after the onset of acute coronary syndrome and should ensure the correct diagnosis of acute coronary syndrome in combination with troponin.
糖原磷酸化酶BB被认为是急性冠脉综合征及时且特异的标志物。最近已发布一种用于常规诊断中检测糖原磷酸化酶BB的试剂盒。
测试糖原磷酸化酶BB检测在急性冠脉综合征诊断中的应用。
对70例疑似急性冠脉综合征患者进行检测。根据欧洲心脏病学会(ESC)/美国心脏病学会(ACC)/美国心脏协会(AHA)标准做出急性冠脉综合征/非冠脉疾病的最终诊断。对所有受试者入院时以及入院后2小时和6小时采集静脉血浆(肝素锂抗凝)中的肌钙蛋白I、肌红蛋白和糖原磷酸化酶BB进行检测。
急性冠脉综合征患者(n = 52)入院时及入院后2小时的糖原磷酸化酶BB水平显著更高(21.9对6.2;18.7对5.9微克/升;p < 0.01)。糖原磷酸化酶BB水平对急性冠脉综合征存在与否的诊断效能高于肌钙蛋白I水平(ROC曲线下阈值0.89对0.78;0.87对0.67)。入院后的头两小时,仅糖原磷酸化酶BB水平作为急性冠脉综合征发生率回归模型中的独立变量(p < 0.05)。当从急性冠脉综合征组中剔除心肌坏死患者组(n = 39;心电图无ST段抬高的急性心肌梗死;非ST段抬高型心肌梗死[NSTEMI])后,发现初次检测及两小时后回归模型中仅糖原磷酸化酶BB和心肌肌钙蛋白I(cTnl)为独立变量。将糖原磷酸化酶BB校正为心肌肌钙蛋白I后,发现非ST段抬高型心肌梗死患者中校正后的糖原磷酸化酶BB水平显著更高(14.5对 -48.0;p < 0.01)。
在急性冠脉综合征发病后的最初数小时内,糖原磷酸化酶BB检测独立于肌钙蛋白具有出色的诊断效能,与肌钙蛋白联合应用应能确保急性冠脉综合征的正确诊断。