About Cardiac Biomarkers
The Tests
Only a few cardiac biomarker tests are routinely used by physicians. The current biomarker test of choice for detecting heart damage is troponin. Other cardiac biomarkers are less specific for the heart and may be elevated in other situations such as skeletal muscle injury.
Current cardiac biomarker tests that may be used to help diagnose, evaluate, and monitor individuals suspected of having acute coronary syndrome (ACS) include:
- Troponin (I or T)—this is the most commonly ordered and most specific of the cardiac markers. It is elevated (positive) within a few hours of heart damage and remains elevated for up to two weeks. Rising levels in a series of troponin tests performed over several hours can help diagnose a heart attack.
- High-sensitivity troponin—this test detects the same protein that the standard test does, just at much lower levels. Because this version of the test is more sensitive, it becomes positive sooner and may help detect ACS earlier than the standard test. The hs-troponin test may also be positive in people with stable angina and even in people with no symptoms. When it is elevated in these individuals, it indicates an increased risk of future heart events such as heart attacks. This test may not be available in all labs.
- Creatine kinase (CK) and CK-MB—in the U.S., CK has been largely replaced by troponin. It may sometimes be used to help detect a second heart attack that occurs shortly after the first. CK-MB is one particular form of the enzyme creatine kinase that is found mostly in heart muscle; it rises when there is damage to the heart muscle cells and may be used in follow up to an elevated CK and/or when the troponin test is not available.
- Myoglobin—this test may be used along with troponin to detect a heart attack early, but in the U.S., it is used less frequently.
Other biomarker tests that may be used include:
- hs-CRP—this test may be used to help determine risk of future heart attacks in people who have already suffered one in the past.
- BNP (or NT-proBNP)—although usually used to recognize heart failure, an increased level in people with ACS indicates an increased risk of recurrent events.
On the horizon: several biomarkers are being investigated for their potential use in helping to evaluate people for ACS. These are currently only used in research settings and are not available in clinical practice.
General lab tests are frequently ordered along with cardiac biomarkers to evaluate a person’s general health status and the current status of the individual’s kidneys, liver, electrolyte and acid/base balance, blood sugar, and blood proteins. They may include:
- Blood gases
- Comprehensive metabolic panel (CMP) or basic metabolic panel (BMP)
- Electrolytes
- Complete blood count (CBC)
Non-laboratory Tests
These tests allow health practitioners to look at the size, shape, and function of the heart as it is beating. They can be used to detect changes to the rhythm of the heart as well as to detect and evaluate damaged tissues and blocked arteries.
- EKG (ECG, electrocardiogram)
- Nuclear scan
- Coronary angiography (or arteriography)
- Echocardiogram (Cardiac echo, transthoracic echocardiography (TTE))
- Stress testing
- Chest X-ray
For more about these, visit the Non-Invasive Tests and Procedures article on the American Heart Association web site.
Table of biomarkers used for diagnosing and monitoring acute coronary syndrome
Marker | what it is | Tissue source | Reason for Increase | Time to Increase | Time Back to Normal | When/How Used |
---|---|---|---|---|---|---|
Cardiac Troponin | Regulatory protein complex; two cardiac-specific isoforms: T and I | Heart | Injury to heart | 3 to 4 hours | Remains elevated for 10 to 14 days | Diagnose heart attack, risk stratification, assist in deciding management, assess degree of damage |
High-sensitivity cardiac troponin | Same as above, just measures the same protein at a much lower level | Heart | Injury to heart | Within 3 hours of onset of symptoms | Same as above | Same as above; may also be elevated in stable angina and people without symptoms and indicates risk of future cardiac events (e.g., heart attacks) |
CK | Enzyme; total of three different isoenzymes | Heart, brain, and skeletal muscle | Injury to skeletal muscle and/or heart cells | 3 to 6 hours after injury, peaks in 18 to 24 hours | 48 to 72 hours, unless due to continuing injury | Frequently performed in combination with CK-MB; sometimes to detect second heart attack occurring shortly after the first |
CK-MB | Heart-related isoenzymes of CK | Heart primarily, but also in skeletal muscle | Injury to heart and/or muscle cells | 3 to 6 hours after heart attack, peaks in 12 to 14 hours | 48 to 72 hours, unless new or continuing damage | Less specific than troponin, may be ordered when troponin is not available |
Myoglobin | Oxygen-storing protein | Heart and other muscle cells | Injury to muscle and/or heart cells | 2 to 3 hours after injury, peaks in 8 to 12 hours | Within one day after injury | Used less frequently; sometimes performed with troponin to provide early diagnosis |
Table of Biomarkers Used for Prognosis
bioMarker | what it is | Reason for Increase | When/How Used |
---|---|---|---|
hs-CRP | Protein | Inflammation | May help determine risk of future cardiac events in those patients who have had a heart attack |
BNP and NT-proBNP | Heart hormone | Heart failure; increased risk of another heart attack | Usually used to recognize heart failure, but an increased level in people with ACS indicates an increased risk of recurrent events |
Related Tests
- Troponin Test (cTN) Learn More
- hs-CRP Test (C-Reactive Protein High-Sensitivity) Learn More
- Brain Natriuretic Peptide Test (BNP and NT-proBNP) Learn More
- American Heart Association: Diagnosing a Heart Attack Learn More
- American Academy of Family Physicians: Heart Attack Learn More
- National Heart Lung and Blood Institute: Heart Attack Learn More
- American Heart Association: Understand Your Risks to Prevent a Heart Attack Learn More
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Robert H. Christenson, Ph.D., DABCC, FACB. Professor of Pathology, Professor of Medical and Research Technology. Director, Rapid Response Laboratories, University of Maryland School of Medicine, Baltimore, Maryland.