Table 1.
The milestones of biomarker discoveries for myocardial infarction.
Years | Milestone | References |
---|---|---|
1954 | AST released from the necrotic cardiac myocytes to the circulation could be helpful in diagnosing AMI | (5) |
1954–1955 | LDH was considered as a useful marker in the diagnosis of AMI | (6, 7) |
1978 | CK activity was considered a better predictor of myocardial injury and an independent indicator in the diagnosis of AMI for 20 years | (8) |
1982 | Myoglobin occurs in the first 30 min while it has less specificity | (9) |
1982 | S100 gradually comes into spotlight and is related to MI | (10–14) |
1992 | Subtypes of IL play crucial roles in diagnosis and prognosis of MI | (15–21) |
1993 | “Decreased immunoreactivity for H-FABP may be a good histological marker of damaged cardiomyocytes” | (22) |
1997 | IGF may protect cardiac function after AMI | (23) |
1998 | cMyC is expressed in the heart specially | (24–27) |
2001 | uACR is associated with increased long-term risk of cardiovascular and total mortality in survivors of MI | (28) |
2003 | Atherosclerosis is proved to be associated with alterations in MMP activity | (29) |
2003 | MiRNAs are associated to MI | (30–41) |
2004 | VEGF is associated with diagnosis, infarction size, and clinical outcomes of MI | (42–45) |
2007 | Hs-cTn is current golden standard for AMI diagnosis | (46) |
2013 | HPA is associated with acute MI accompanied with elevated white blood cell count | (47) |
2013 | Copeptin: a new marker in cardiology | (48) |
2014 | Ischemia-reperfusion injury has been proved to decrease MG53 in heart | (49) |
2015 | PIK3C2A could affect angiogenesis contributing to the pathophysiology of coronary artery disease | (50) |
AST, aspartate aminotransferase; LDH, lactate dehydrogenase; CK, creatine kinase; IL, interleukin; H-FABP, heart type fatty acid-binding protein; IGF, insulin-like growth factor 1; cMyC, cardiac myosin-binding protein C; VEGF, vascular endothelial growth factor; hs-cTn, high sensitivity cardiac troponin; HPA, heparanase.