Sensitive, rapid assay of subforms of creatine kinase MB in plasma.
Open Access
- 1 July 1989
- journal article
- research article
- Published by Oxford University Press (OUP) in Clinical Chemistry
- Vol. 35 (7) , 1452-1455
- https://doi.org/10.1093/clinchem/35.7.1452
Abstract
The subforms of creatine kinase (CK; EC 2.7.3.2) in plasma have received recent attention as potential markers for the early diagnosis of acute myocardial infarction. Because changes in CK-MM subforms are not specific for myocardial injury, we developed an assay, based on high-voltage electrophoresis, that is sufficiently sensitive to detect the CK-MB subforms at concentrations substantially below the upper limit of normal (14 U/L). The assay can detect 1.25 U of either MB subform per liter with a precision of 0.20 U/L and gives responses that vary linearly with activity concentration from 0.0 through 30.0 U/L, with an identical signal response for both subforms. When both subforms are present in a serum sample, the assay accurately measures both the relative percentage and the absolute quantity of each: assay activity/known activity was 1.03 for each subform at a total MB subform activity of 5.0 U/L (r = 0.98). Assay time is 25 min, and there is no loss of CK during electrophoresis. Thus, this system can be used to rapidly, sensitively, and precisely quantify the two CK-MB subforms at activities well within the normal reference interval.This publication has 3 references indexed in Scilit:
- Sensitivity of Routine Clinical Criteria for Diagnosing Myocardial Infarction Within 24 Hours of HospitalizationAnnals of Internal Medicine, 1987
- Creatine kinase isoenzyme MM variants in skeletal muscle and plasma from marathon runners.Clinical Chemistry, 1986
- Purification and characterization of naturally occurring and in vitro induced multiple forms of MM creatine kinase.Journal of Biological Chemistry, 1984