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Published on: August 8, 2013
Evaluation of CK-MB isoform analysis for early diagnosis of myocardial infarction
J L Bock1, G X Brogan, C F McCuskey
1Department of Pathology, State University of New York at Stony Brook, USA.
Insights
High-voltage electrophoresis of creatine kinase-MB (CK-MB) and its isoforms offers a sensitive method for early myocardial infarction (MI) detection. Isoform analysis significantly enhances early sensitivity for diagnosing heart attacks.
Area of Science:
- Clinical Chemistry
- Cardiology
- Diagnostic Medicine
Background:
- Early detection of myocardial infarction (MI) is crucial for timely intervention.
- Creatine kinase-MB (CK-MB) and its isoforms are established biomarkers for cardiac injury.
- High-voltage electrophoresis offers a method for precise CK-MB isoform analysis.
Purpose of the Study:
- To prospectively evaluate the diagnostic performance of CK-MB and its isoforms using high-voltage electrophoresis.
- To assess the sensitivity and specificity of this method for early detection of MI in emergency department patients.
Main Methods:
- Prospective study involving 231 patients with symptoms suggestive of ischemic chest pain.
- Plasma samples collected at 0, 1, and 3 hours post-presentation.
- Analysis of total CK-MB and isoforms (MB2/MB1 ratio) via high-voltage electrophoresis.
Main Results:
- The combined CK-MB and isoform test achieved 68% overall sensitivity and 92% specificity.
- The test was positive within 3 hours in 92% of confirmed MI cases.
- Isoform analysis improved early sensitivity (55% within 3 hours) compared to total CK-MB alone (39%).
Conclusions:
- Analysis of CK-MB and its isoforms by high-voltage electrophoresis is an effective tool for rapid MI diagnosis.
- Isoform analysis significantly enhances the sensitivity of early MI detection.
- This method provides a valuable approach for timely and accurate diagnosis of acute cardiac events.
Abstract:
Measurement of CK-MB and its isoforms by high-voltage electrophoresis has been proposed as a sensitive test for early detection of myocardial infarction (MI). We performed a prospective study of this test in 231 patients presenting to the Emergency Department with symptoms consistent with ischemic chest pain. Blood specimens were obtained at 0, 1, and 3 h following presentation, and plasma was immediately frozen and analyzed within 1 week by high-voltage electrophoresis for total CK-MB and isoforms. The test was considered positive whenever total CK-MB was elevated (>6 U/L) or the cardiac isoform MB2 was relatively increased (MB2 > 2 U/L and MB2/MB1 > 1.7). This test had a sensitivity of 68% overall and 55% for specimens collected within 3 h of symptom onset. It was positive within 3 h of presentation in 36/39 (92%) of patients with confirmed MI. Specificity was 92% overall and did not vary with time after symptoms. The CK-MB alone, at the cutoff of 6 U/L, had lower sensitivity overall (56%; p = 0.01) and within 3 h of onset (39%; p = 0.03), and higher specificity overall (98%; p < 0.001). Lowering the cutoff for CK-MB alone to match the sensitivity of the isoform test caused a greater loss of specificity. It is concluded that analysis of CK-MB by high-voltage electrophoresis is an effective method for rapid diagnosis of MI, with the isoform analysis enhancing early sensitivity.
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