Department of Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Department of Cardiovascular Surgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Ann Thorac Surg. 2019 Oct;108(4):1195-1201. doi: 10.1016/j.athoracsur.2019.03.072. Epub 2019 Apr 26.
Cardiac surgical procedures produce iatrogenic myocardial cell injury with necrosis that result in an obligatory release of biomarkers. Cardiac myosin binding protein C (cMyBP-C) has recently emerged as a specific and sensitive biomarker in patients with acute myocardial injury. We therefore aimed to investigate the release profiles of cMyBP-C after cardiac surgical procedures.
Enzyme-linked immunosorbent assay to detect blood cMyBP-C was established by using two monoclonal antibodies against N-terminus of human cMyBP-C. Consecutive patients undergoing cardiac operations (N = 151) were recruited in this study. Blood cMyBP-C was assayed preoperatively, at intensive care unit arrival (0 hour after the operation), at 2 to 48 hours, and before discharge. The characteristics and detailed surgical procedure were recorded.
The established immunoassay was capable of detecting human cMyBP-C (0 to 1000 ng/L). The released cMyBP-C peaked immediately after cardiac surgery (0 h), attaining 3.8-fold higher than before the operation, dropped abruptly within 24 hours, and stayed at a higher level until discharge. Postoperative cMyBP-C levels correlated positively with high-sensitivity cardiac troponin T (hs-cTnT), creatine kinase, myoglobin, and creatine kinase MB isoenzyme. Different cardiac surgical procedures were characterized by different levels of release of cardiac biomarkers. Isolated off-pump coronary artery bypass grafting was associated with the smaller amount of cMyBP-C release, whereas valve replacement/plasty surgery produced higher release, in particular the multiple-valve surgery. Both cMyBP-C and hs-cTnT correlated with surgical techniques, postoperative intensive care unit stay, and hospital stay.
Circulating cMyBP-C is a promising novel biomarker for evaluating cardiac surgical trauma in patients undergoing a cardiac operation.
心脏外科手术会导致医源性心肌细胞损伤和坏死,从而导致生物标志物的必然释放。心肌肌球蛋白结合蛋白 C(cMyBP-C)最近已成为急性心肌损伤患者的一种特异性和敏感性生物标志物。因此,我们旨在研究心脏外科手术后 cMyBP-C 的释放情况。
使用针对人 cMyBP-C N 端的两种单克隆抗体,建立了用于检测血液 cMyBP-C 的酶联免疫吸附测定法。本研究纳入了连续接受心脏手术的患者(n=151)。在术前、重症监护病房到达时(手术后 0 小时)、2 至 48 小时以及出院前检测血液 cMyBP-C。记录特征和详细的手术过程。
所建立的免疫测定法能够检测人 cMyBP-C(0 至 1000ng/L)。cMyBP-C 在心脏手术后立即释放(0 小时),达到术前的 3.8 倍,在 24 小时内迅速下降,并在出院前保持在较高水平。术后 cMyBP-C 水平与高敏心肌肌钙蛋白 T(hs-cTnT)、肌酸激酶、肌红蛋白和肌酸激酶 MB 同工酶呈正相关。不同的心脏手术过程具有不同的心脏生物标志物释放水平。非体外循环冠状动脉旁路移植术与较少的 cMyBP-C 释放相关,而瓣膜置换/成形术产生了更高的释放,特别是多瓣膜手术。cMyBP-C 和 hs-cTnT 均与手术技术、术后重症监护病房停留时间和住院时间相关。
循环 cMyBP-C 是评估心脏手术创伤的一种很有前途的新型生物标志物,适用于接受心脏手术的患者。