Melanson Stacy E F, Morrow David A, Jarolim Petr
Department of Pathology, Division of Clinical Laboratories, Harvard Medical School, Boston, MA, USA.
Am J Clin Pathol. 2007 Aug;128(2):282-6. doi: 10.1309/Q9W5HJTT24GQCXXX.
Cardiac troponins are important biochemical markers for defining the presence of myocardial injury. However, limitations in troponin testing exist, including the relatively late increase in troponin after onset of ischemia. We therefore evaluated a more sensitive troponin assay for detection of myocardial injury in "early presenters." Discarded serial specimens were obtained from 103 patients who had a negative cardiac troponin I (cTnI) result followed by a positive cTnI result. Results were obtained using our current cTnI method and a new more sensitive assay, TnI-Ultra (Siemens Medical Solutions, Diagnostics Division, Tarrytown, NY). Medical records were reviewed to determine the clinical diagnosis. Precision studies yielded a 10% coefficient of variation at the diagnostic cut points for cTnI (0.10 ng/mL [0.10 microg/L]) and TnI-Ultra (0.04 ng/mL [0.04 microg/L]). TnI-Ultra was positive before cTnI in 66 (64.1%) of 103 cases. We conclude that the more sensitive assay, TnI-Ultra, has better analytic performance and has the potential to detect myocardial injury earlier than the current cTnI assay.
心肌肌钙蛋白是确定心肌损伤存在的重要生化标志物。然而,肌钙蛋白检测存在局限性,包括缺血发作后肌钙蛋白升高相对较晚。因此,我们评估了一种更敏感的肌钙蛋白检测方法,用于检测“早期就诊者”的心肌损伤。从103例心肌肌钙蛋白I(cTnI)结果为阴性随后为阳性的患者中获取废弃的系列标本。使用我们当前的cTnI方法和一种新的更敏感的检测方法TnI-Ultra(西门子医疗解决方案公司诊断部,纽约塔里敦)获得结果。查阅病历以确定临床诊断。精密度研究得出,cTnI(0.10 ng/mL [0.10 μg/L])和TnI-Ultra(0.04 ng/mL [0.04 μg/L])诊断切点处的变异系数为10%。在103例病例中的66例(64.1%)中,TnI-Ultra在cTnI之前呈阳性。我们得出结论,更敏感的检测方法TnI-Ultra具有更好的分析性能,并且有可能比当前的cTnI检测方法更早地检测到心肌损伤。