Detection of macro-creatine kinase and macroamylase by polyethylene glycol precipitation and ultrafiltration methods
Macroenzymes may cause elevations in serum enzyme activity. Macroenzymes are not common; however their detection is important because they cause diagnostic confusion and therapeutic errors. We analyzed 2 of the most prevalent macroenzymes in the literature, macro-creatine kinase (macro-CK) and macro...
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Published in | Clinica chimica acta Vol. 412; no. 23-24; pp. 2052 - 2057 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
20.11.2011
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Subjects | |
Online Access | Get full text |
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Summary: | Macroenzymes may cause elevations in serum enzyme activity. Macroenzymes are not common; however their detection is important because they cause diagnostic confusion and therapeutic errors.
We analyzed 2 of the most prevalent macroenzymes in the literature, macro-creatine kinase (macro-CK) and macroamylase, using 2 methods for detection, polyethylene glycol (PEG) precipitation and ultrafiltration (UF). Enzyme measurements were made using a Roche Modular Analytics P analyzer. Imprecision was assessed using quality control material. We evaluated 125 samples from apparently healthy subjects to establish reference intervals. For macro-CK comparison, 94 samples with activities>200U/l were analyzed with both PEG precipitation and UF and compared to electrophoresis. PEG precipitation and UF were compared for macroamylase detection using 130 samples with amylase activities>110U/l.
UF was more precise and demonstrated narrower reference intervals for both analytes. PEG precipitation and UF were able to detect true cases of macro-CK with overall agreement with electrophoresis of 79.8% and 80.9%, respectively. Both methods detected the same number of ‘positive’ macroamylase samples; however PEG precipitation resulted in a greater number of ‘indeterminate’ cases.
This is the first report where UF has been shown useful for the detection of both macro-CK and macroamylase. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0009-8981 1873-3492 1873-3492 |
DOI: | 10.1016/j.cca.2011.01.023 |