Abstract
The enzyme β-enolase (αβ and ββ forms) is present in skeletal and heart muscle and catalyses the glycolysis of 2-phosphoglycerate to phosphoenolpyruvate. The enzyme was measured in serum samples from patients with acute myocardial infarction, angina pectoris, congestive heart failure, and idiopathic cardiomyopathy. Serum concentrations of β-enolase were significantly increased in acute myocardial infarction but not in the other cardiovascular diseases. Activity peaked approximately 12 to 14 hours after an acute attack of chest pain, and then gradually decreased as the patient recovered. The rise and fall in β-enolase concentration were faster and steeper than those of creatine kinase activity, particularly in patients in whom activities of both these enzymes were less high. The assay of β-enolase, which is highly specific and sensitive, has considerable advantages for the early diagnosis of myocardial infarction and the diagnosis of a second episode of myocardial infarction because β-enolase concentration increases very early and rapidly and clears quickly. These data imply that serum β-enolase may be a more effective marker for early myocardial infarction, particularly in milder cases, than measurement of creatine kinase activity.
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CITATION STYLE
Nomura, M., Kato, K., Nagasaka, A., Shiga, Y., Miyagi, Y., Fukui, R., … Nakai, A. (1987). Serum β-enolase in acute myocardial infarction. British Heart Journal, 58(1), 29–33. https://doi.org/10.1136/hrt.58.1.29
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