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Heart-type, fatty-acid binding protein can be a diagnostic marker in acute coronary syndromes
Umut Cavus1, Figen Coskun, Bunyamin Yavuz
1Departments of Emergency Medicine, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Insights
Heart-type fatty acid-binding protein (H-FABP) shows high sensitivity and specificity for early acute coronary syndrome (ACS) diagnosis. This biomarker aids in rapid, bedside detection of myocardial injury within 20 hours of symptom onset.
Area of Science:
- Cardiology
- Biomarker Discovery
- Emergency Medicine
Background:
- Acute coronary syndrome (ACS) diagnosis relies on cardiac biomarkers like troponins, CK-MB, and myoglobin.
- These traditional markers often lack sensitivity in the early hours of ACS, delaying diagnosis.
- There is a need for more effective early diagnostic tools for chest pain evaluation.
Purpose of the Study:
- To evaluate the efficacy of heart-type fatty acid-binding protein (H-FABP) compared to CK-MB and myoglobin for the early diagnosis of ACS.
- To assess the sensitivity and specificity of H-FABP in the initial hours of suspected myocardial injury.
Main Methods:
- A study involving 67 patients diagnosed with ACS.
- Initial blood samples analyzed for CK-MB, troponin T (cTnT), myoglobin, and H-FABP.
- Serial ECGs and cardiac enzyme samples collected at 4, 8, and 12 hours post-admission.
- H-FABP levels were re-assessed at the 4-hour mark.
Main Results:
- H-FABP demonstrated high sensitivity (97.6%) in the first hour, comparable to CK-MB (96.7%) and superior to myoglobin (85.4%).
- H-FABP exhibited superior specificity (38.5%) at the first hour compared to CK-MB (34.6%), myoglobin (34.6%), and troponin T (23.1%).
- These performance trends for H-FABP were maintained up to the fourth hour of myocardial injury.
Conclusions:
- H-FABP is a sensitive and specific biomarker for the early diagnosis of ACS.
- Point-of-care H-FABP testing offers advantages of rapid, bedside results for patients presenting with chest pain.
- H-FABP measurement is recommended for patients with suspected ACS within 20 hours of symptom onset.
Objectives:
Chest pain is one of the most common complaints among patients admitted to emergency departments. Cardiac troponins, CK-MB and myoglobin, which are used routinely in the diagnosis of acute coronary syndrome (ACS), are not elevated in the initial hours of ACS--precluding their usefulness in the early diagnosis. The aim of this study is to determine the efficacy of H-FABP compared to myoglobin and CK-MB in the early diagnosis of ACS.
Methods:
Sixty-seven patients with ACS were enrolled in the study. An initial blood sample was obtained for CK-MB, cTnT, myoglobin and H-FABP. At the fourth, eighth, and 12th hours, repeat ECGs and cardiac enzyme samples were obtained. H-FABP test was repeated at the fourth hour.
Results:
H-FABP has sensitivity equal to that of CK-MB and superior to that of myoglobin (97.6%, 96.7%, 85.4%, respectively) on the first hour. This trend extends to the fourth hour of myocardial injury as well. H-FABP was more specific than CK-MB, myoglobin and troponin T at the first hour (38.5%, 34.6%, 34.6%, 23.1%, respectively), whereas its specificity at the fourth hour was equal to those of CK-MB and troponin T and exceeded that of myoglobin.
Conclusions:
It can be suggested that in patients with an initial diagnosis of ACS and within 20 hours from symptom onset, H-FABP levels may be measured. For this purpose, point-of-care H-FABP test may be utilized, which has the advantage of bedside testing and rapid test results.
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