CREATINE-KINASE MB DURING MYOCARDIAL-INFARCTION - RELATIONSHIP TO PREEXISTING CORONARY HEART-DISEASE AND MEDICATION

Citation
H. Sax et al., CREATINE-KINASE MB DURING MYOCARDIAL-INFARCTION - RELATIONSHIP TO PREEXISTING CORONARY HEART-DISEASE AND MEDICATION, Acta cardiologica, 52(5), 1997, pp. 423-430
Citations number
23
Categorie Soggetti
Cardiac & Cardiovascular System
Journal title
ISSN journal
00015385
Volume
52
Issue
5
Year of publication
1997
Pages
423 - 430
Database
ISI
SICI code
0001-5385(1997)52:5<423:CMDM-R>2.0.ZU;2-I
Abstract
Creatine kinase (CK) and its isoenzyme CK-MB are important tools for t he diagnosis of acute myocardial infarction. The content of CK-MB rela tive to total CK in myocardial cells is variable; it is low in normal myocardium and increased several-fold in hypoxic myocardium. We tested the hypothesis that CK-MB mass (CK-MBm) could be related to cardiovas cular history, preinfarctional medication and clinical course during m yocardial infarction. In a prospective study CK and CK-MBm were measur ed 0, 6, 12, 18, 24, 48 and 72 h after the admission to the coronary c are unit. Peak values and areas under the curve (AUC) were determined and normalized for total CK activity (CK-MBm/CK). Of 185 patients with acute chest pain, 70 patients had 71 acute myocardial infarctions and were enrolled in the study. A history of chronic angina pectoris or h ypertension had no influence on CK-MBm/CK levels. In contrast, treatme nt with beta-blockers before infarction resulted in a lower relative C K-MBm peak value (CK-MBm/CK 6.0 (median value), range 3.1-15.3, versus 7.0, range 0.5-17.3; p < 0.05). Other drugs had no influence. Patient s with persistent pain on admission tended to have higher relative CK- MBm values (peak CK-MBm/CK: 68, range 0.5-17.3, versus 5.3, range 1.4- 7.9, p = 0.08; AUC CK-MBm/CK: 0.05, range 0.01-0.10, versus 0.03, rang e 0.01-0.06, p < 0.05). Three vessel disease on coronary angiography w as associated with higher CK-MBm/CK values during the acute phase of m yocardial infarction that those with 1-2 vessel disease (Peak CK-MBm/C K: 7.9, range 5.5-17.3, versus 6.4, range 3.1-10.1, p < 0.05; AUC CK-M Bm/CK: 0.06, range 0.02-0.11, versus 0.04, range 0.02-0.07, p < 0.05). We conclude that relative CK-MBm/CK levels reflect to a certain degre e the extent of the coronary disease and that preinfarctional beta-blo ckade may result in lower CK-MBm levels.