Variability of Lipoprotein-Associated Phospholipase A2 Measurements
Author(s) -
Joseph P. McConnell,
Allan S. Jaffe
Publication year - 2008
Publication title -
clinical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.705
H-Index - 218
eISSN - 1530-8561
pISSN - 0009-9147
DOI - 10.1373/clinchem.2008.103358
Subject(s) - lipoprotein associated phospholipase a2 , myocardial infarction , biomarker , inflammation , phospholipase a2 , lipoprotein , medicine , cardiology , stroke (engine) , lipoprotein(a) , acute phase protein , coronary heart disease , phospholipase , bioinformatics , chemistry , biology , enzyme , biochemistry , cholesterol , physics , thermodynamics
We read with interest the recent report in this journal by Khuseyinova and colleagues regarding the variability of serial lipoprotein-associated phospholipase A2 (Lp-PLA2) measurements in postmyocardial infarction patients(1). Because Lp-PLA2 plays a role in inflammation but, unlike other inflammatory proteins, is not an acute-phase reactant(2), nonspecificity issues associated with acute-phase reactants may be averted. Indeed, recent reviews verify that several epidemiologic studies have demonstrated a strong association between Lp-PLA2 and ischemic events(2)(3)(4). Thus, as indicated by Khuseyinova and colleagues, Lp-PLA2 appears to be a promising emerging biomarker for coronary heart disease and stroke. We applaud the effort of this group to evaluate the performance of Lp-PLA2 measurements.With all assay development, multiple iterations of assays are often developed before a given …
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