Markers for early detection of cardiac diseases
1Department of Laboratory Medicine University of California, San Francisco, CA, USA. awu@harthosp.org
Insights
New biomarkers show promise for early detection of acute coronary syndromes (ACS) in emergency departments. These novel markers may aid in timely diagnosis and treatment decisions for patients presenting with chest pain.
Area of Science:
- Cardiology
- Biomarker Discovery
- Emergency Medicine
Background:
- Current myocardial necrosis markers (troponin, CK-MB, myoglobin) are often negative in early acute coronary syndromes (ACS).
- Timely diagnosis and risk stratification are crucial for patients presenting to the emergency department (ED) within 3 hours of chest pain onset.
- Existing biomarkers lack the sensitivity for early ACS detection, necessitating research into novel diagnostic tools.
Purpose of the Study:
- To identify and evaluate novel biomarkers for the early diagnosis and risk stratification of acute coronary syndromes (ACS).
- To explore potential new diagnostic markers that can be utilized during initial emergency department (ED) presentations.
Main Methods:
- Review of active research identifying several classes of promising biomarkers for early ACS detection.
- Categorization of novel biomarkers based on their proposed mechanism: inflammation, plaque instability, platelet activation, and myocardial ischemia.
- Assessment of the utility of each biomarker class in diagnosing ACS during the critical early hours.
Main Results:
- Several classes of biomarkers show potential for early ACS detection, including those related to inflammation (hs-CRP, MPO), plaque instability (PAPP-A, PGF), platelet activation (whole blood choline, CD40L), and ischemia (IMA, FFAs, serum choline, BNP).
- Each investigated biomarker class demonstrated some diagnostic utility for early ACS identification.
- No single novel biomarker currently possesses sufficient specificity for routine myocardial disease diagnosis.
Conclusions:
- Novel biomarkers offer potential for improved early diagnosis and risk stratification of acute coronary syndromes (ACS).
- A multi-marker approach may be necessary to enhance diagnostic accuracy and specificity for myocardial disease.
- Further research and validation are required for the routine clinical application of these promising biomarkers.
Abstract:
The existing markers for myocardial necrosis, such as cardiac troponin, creatine kinase-MB, and myoglobin are thought to be released into blood following irreversible myocardial necrosis. Thus results of these tests are usually negative for patients with acute coronary syndromes (ACS) who present to the emergency department (ED) within the first 3 hours after the onset of chest pain. Given the need to make early therapeutic and triage decisions, biomarkers that can be used to diagnose and/or risk stratify ACS patients during their initial ED presentation will be important. Active research in this area has identified several classes of biomarkers that show promise for early detection of disease. These include tests for the presence of acute inflammation and infiltration (e.g., high sensitivity-C-reactive protein, myeloperoxidase), plaque instability (e.g., pregnancy-associated plasma protein-A, placental growth factor), platelet activation (e.g., whole blood choline, platelet density, CD40 ligand), and myocardial ischemia (e.g., ischemia modified albumin, free fatty acids, serum choline, and B-type natriuretic peptide). Each of these tests has demonstrated some utility for early diagnosis. However, as most lack specificity for myocardial disease, routine use may require a multi-marker approach.
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