E. Bonnefoy et al., MYOGLOBIN AND CPK-MM ISOFORMS DURING ACUT E MYOCARDIAL-INFARCTION, Archives des maladies du coeur et des vaisseaux, 86(9), 1993, pp. 1367-1371
The biological diagnosis is usually late with respect to clinical and
electrocardiographic signs of acute myocardial infarction. Recent labo
ratory methods have stimulated renewed interest in very early marker o
f infarction : myoglobin and CPK isoforms. The authors undertook a pro
spective study of the diagnostic sensitivity of myoglobin (MG), CPK an
d CPK-MM isoforms in 30 consecutive patients undergoing intravenous th
rombolytic therapy in the acute phase of myocardial infarction. Blood
samples were obtained on admission and every 30 minutes for 1 h 30. Th
e Mb contributed to diagnosis of infarction on admission in 89 % of pa
tients. This percentage fell to 44 % for the ratio MM3/MM1 > 0.5 to 27
% for the CPK and to 24 % for the ratio MM3/MM1 > 1. The sensitivity
of all tests increased in the later blood samples but it remained low
in the CPK and MM3/MM1 > 1 criteria. The diagnostic sensitivity of the
first sample was also better in patients admitted after the 3rd hour
(Mb = 100 %; MM3/MM1 > 0.5: 58 %; CPK: 41 %) compared with those admit
ted before the 3rd hour (Mb = 82 %; MM3/MM1 > 0.5: 35 %; CPK: 17 %). T
hese results show that the diagnostic sensitivity of biological marker
s of myocardial infarction is very different. The serum myoglobin is a
n earlier and more sensitive marker than the CPK or CPK-MM isoforms.