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Updated: Sep 21, 2026

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Published on: August 8, 2013
Release of heart fatty acid-binding protein into plasma after acute myocardial infarction in man
A H Kleine1, J F Glatz, F A Van Nieuwenhoven
1Department of Physiology, University of Limburg, Maastricht, The Netherlands.
Insights
Heart fatty acid-binding protein (H-FABP) is a more suitable early indicator for acute myocardial infarction (AMI) than CK-MB or alpha-HBDH. H-FABP levels rise significantly within 3 hours of AMI onset, aiding faster diagnosis.
Area of Science:
- Biochemistry
- Cardiology
- Clinical Diagnostics
Background:
- Acute myocardial infarction (AMI) diagnosis relies on detecting cardiac biomarkers.
- Current biomarkers like CK-MB and alpha-HBDH have limitations in early detection.
- Heart fatty acid-binding protein (H-FABP) is a potential early diagnostic marker.
Purpose of the Study:
- To evaluate the diagnostic utility of H-FABP for early detection of AMI.
- To compare the release kinetics of H-FABP with established cardiac enzymes (CK-MB, alpha-HBDH).
Main Methods:
- Development of a sensitive sandwich ELISA for human H-FABP quantification in plasma.
- Measurement of plasma H-FABP, CK-MB, and alpha-HBDH levels in AMI patients.
- Comparison of biomarker levels against established normal thresholds and time of symptom onset.
Main Results:
- H-FABP levels significantly elevated within 3 hours post-AMI, exceeding normal thresholds.
- Peak H-FABP levels observed at 4.1 hours, compared to 8.4 hours for CK-MB and 25 hours for alpha-HBDH.
- H-FABP detected above threshold in 18/22 patients within 3.5 hours, versus 9/22 for CK-MB and 6/22 for alpha-HBDH.
Conclusions:
- H-FABP is released rapidly and substantially from the heart following myocardial infarction.
- H-FABP demonstrates superior sensitivity and earlier detection capability for AMI compared to CK-MB and alpha-HBDH.
- H-FABP is a promising biomarker for early diagnosis of acute myocardial infarction.
Abstract:
The release of cytoplasmic heart fatty acid-binding protein (H-FABP) into the plasma of cardiac patients up to 38 hr after the onset of the first clinical symptoms of acute myocardial infarction (AMI) was studied, using a sensitive direct and noncompetitive Enzyme Linked Immunosorbent Assay of the antigen capture type (sandwich ELISA), newly developed for the measurement of small amounts of human H-FABP in plasma samples. Plasma levels of H-FABP were compared with plasma activity levels of the myocardial cytoplasmic enzymes creatine kinase MB (CK-MB) and alpha-hydroxybutyrate dehydrogenase (alpha-HBDH). Upper normal levels of H-FABP (19 micrograms/l), CK-MB (10 U/l) and alpha-HBDH (160 U/l) as determined in plasma from 72 blood donors served as threshold levels. H-FABP levels were significantly elevated above their threshold level within 3 hr after AMI. Peak levels of H-FABP, CK-MB and alpha-HBDH were reached 4.1 +/- 0.9 hr, 8.4 +/- 1.4 hr and 25.0 +/- 9.5 hr (means +/- S.D., n = 10) after acute myocardial infarction, respectively. Serial time curves of the plasma contents of H-FABP reveal that after myocardial infarction H-FABP is released in substantial amounts from human hearts. In 18 out of 22 patients with established AMI the plasma FABP level was at or above the threshold level in blood-samples taken within 3.5 hr after the first onset of symptoms of AMI, while for CK-MB this applied to 9 patients and for alpha-HBDH to 6 patients. These findings suggest that for an early indication of acute myocardial infarction in man cytoplasmic heart fatty acid-binding protein is more suitable than heart type creatine kinase MB and/or alpha-hydroxybutyrate dehydrogenase.
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