Risk stratification in patients with unstable angina using absolute serial changes of 3 high-sensitive troponin
Tobias Reichlin1, Raphael Twerenbold, Claudia Maushart
1Department of Cardiology, University Hospital Basel, Basel, Switzerland.
Insights
Most unstable angina (UA) patients show no significant high-sensitivity cardiac troponin (hs-cTn) changes. However, UA patients with hs-cTn changes face a worse prognosis, indicating potential myocardial necrosis.
Area of Science:
- Cardiology
- Biomarker Research
- Emergency Medicine
Background:
- Unstable angina (UA) diagnosis and its association with myocardial necrosis remain unclear.
- High-sensitivity cardiac troponin (hs-cTn) assays are crucial for detecting myocardial injury.
- This study investigates hs-cTn patterns in UA compared to acute myocardial infarction (AMI) and noncardiac chest pain (NCCP).
Purpose of the Study:
- To determine if unstable angina (UA) is associated with previously undetected low-level myocardial necrosis.
- To compare myocardial necrosis patterns in UA, AMI, and NCCP using three hs-cTn assays.
- To assess the prognostic significance of hs-cTn changes in UA patients.
Main Methods:
- A multicenter study enrolled 842 patients with acute chest pain.
- Three hs-cTn assays (Roche hs-cTnT, Beckman Coulter hs-cTnI, Siemens hs-cTnI) were used.
- hs-cTn levels were measured at presentation and at 1, 2, 3, and 6 hours; final diagnoses were adjudicated.
Main Results:
- A ≥2 ng/L hs-cTn change within 1 hour was observed in 26-32% of UA patients, versus 91-96% in AMI and 12-23% in NCCP.
- This hs-cTn change in UA was linked to increased 30-day and 2-year risks of death or recurrent AMI.
- P-values indicate significant differences between UA and AMI, but not between UA and NCCP for hs-cTn changes.
Conclusions:
- Most unstable angina (UA) patients do not exhibit significant high-sensitivity cardiac troponin (hs-cTn) level changes.
- A minority of UA patients with hs-cTn changes experience significantly worse short- and long-term outcomes.
- These findings suggest that hs-cTn changes in UA may indicate a higher risk of adverse events.
Background:
It is unknown whether unstable angina (UA) results in previously nondetectable low-level myocardial necrosis. We compared the pattern of myocardial necrosis between patients with UA, acute myocardial infarction (AMI), and noncardiac chest pain (NCCP) using 3 high-sensitive cardiac troponin (hs-cTn) assays.
Methods:
In a multicenter study, we enrolled 842 unselected patients with acute chest pain in the emergency department. Roche hs-cTnT, Beckman Coulter hs-cTnI, and Siemens hs-cTnI were determined in a blinded fashion at presentation and after 1, 2, 3, and 6 hours. The final diagnosis was adjudicated by 2 independent cardiologists.
Results:
A change in hs-cTn of ≥2 ng/L within the first hour after presentation as assessed with Roche hs-cTnT, Beckman Coulter hs-cTnI, and Siemens hs-cTnI was observed in 26%, 31%, and 32% of patients with UA (n = 115) compared with 91%, 92%, and 96% in patients with AMI (n = 120) and 12%, 23%, and 16% in patients with NCCP (n = 415; P < .001 for all comparisons between UA and AMI, P > .05 for all comparisons between UA and NCCP). In patients with UA, such a 1-hour change in hs-cTn of ≥2 ng/L was associated with an increased risk of death or AMI during the 30-day follow-up (P = .003, .03, .03) and 2-year follow-up (P < .001, .002, and .006).
Conclusions:
In marked contrast to patients with AMI, most patients with UA do not exhibit relevant hs-cTn changes. The minority of UA with hs-cTn changes, however, has a significantly worse short- and long-term outcome.
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