The acute coronary syndromes represent a continuum of myocardial ische
mia ranging from angina, reversible tissue injury --> unstable angina,
frequently associated with minor myocardial damage --> myocardial inf
arction and extensive tissue necrosis. Historically, coronary artery d
isease assessment has been mainly binary, using WHO criteria of sympto
ms, electrocardiography, and biochemical markers. The creatine kinase-
MB isoenzyme (CK-MB) has been a benchmark for markers, but it is not s
pecific for myocardium. Cardiac-specific isoforms of troponin T and I
have emerged as sensitive myocardial infarction (MI) indicators and, i
mportantly, for risk stratification of acute coronary syndrome patient
s. In addition to markers of myocardial cell necrosis, markers of plaq
ue disruption (C-reactive protein and serum amyloid A), ''angry'' plat
elets (P-selectin), ischemia (glycogen phosphorylase-BB isoenzyme), an
d the procoagulant state and thrombosis (soluble fibrin) have potentia
l use. Also, CK-MB and myoglobin have been combined with clinical indi
cators for monitoring reperfusion after thrombolytic therapy. Biochemi
cal markers will continue to be an important clinical adjunct for MI d
iagnosis, risk assessment, and reperfusion monitoring in the future.