Craigavon Cardiac Centre, Southern Trust, Northern Ireland, UK.
Biomark Med. 2010 Jun;4(3):385-93. doi: 10.2217/bmm.10.16.
The diagnosis of acute myocardial infarction currently rests on the measurement of troponin, a biomarker of myocardial necrosis. Unfortunately, the current generation troponin assays detect troponin only 6-9 h after symptom onset. This can lead to a delay in diagnosis and also excessive resource utilization when triaging patients who, ultimately, have noncardiac causes of acute chest pain. For these reasons, there has been extensive research interest in biomarkers that can detect and rule out myocardial infarction early after symptom onset. These include markers of myocardial injury, such as myoglobin, heart-type fatty acid binding protein, glycogen phosphorylase BB; hemostatic markers, such as D-dimer; and finally, inflammatory markers, such as matrix metalloproteinase 9. Recently, highly sensitive troponin assays have reported an early sensitivity for myocardial infarction of greater than 95%, although at a cost of reduced specificity. The optimal strategy with which to use these novel biomarkers and highly sensitive troponins has yet to be determined, and interpretation of their results in light of thorough clinical assessment remains essential.
目前,急性心肌梗死的诊断依赖于肌钙蛋白的测量,肌钙蛋白是心肌坏死的生物标志物。不幸的是,目前的肌钙蛋白检测方法仅在症状发作后 6-9 小时才能检测到肌钙蛋白。这可能导致诊断延迟,并在对最终因非心脏原因引起急性胸痛的患者进行分诊时过度利用资源。出于这些原因,人们对能够在症状发作后早期检测和排除心肌梗死的生物标志物进行了广泛的研究。这些标志物包括心肌损伤标志物,如肌红蛋白、心脏型脂肪酸结合蛋白、糖原磷酸化酶 BB;止血标志物,如 D-二聚体;最后是炎症标志物,如基质金属蛋白酶 9。最近,高敏肌钙蛋白检测方法报告了心肌梗死的早期敏感性大于 95%,尽管特异性降低。尚未确定如何使用这些新型生物标志物和高敏肌钙蛋白的最佳策略,根据全面的临床评估对其结果进行解释仍然至关重要。