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Brief Communications |
1 Department of Internal Medicine, Division of Cardiology, 2 Central Institute for Medical and Chemical Laboratory Diagnostics, 3 Department of Neurology, and 4 Department of Internal Medicine, Division of General Internal Medicine, Innsbruck Medical University, Innsbruck, Austria;
aaddress correspondence to this author at: Universitaetsklinik fuer Innere Medizin III – Kardiologie, Anichstrasse 35, A-6020 Innsbruck, Austria. Fax +43 512 504 22767; e-mail Johannes.Mair{at}i-med.ac.at
Abstract
Background: Soluble CD40 ligand (sCD40L) has been proposed as a new risk marker for cardiovascular diseases; however, its possible role as a diagnostic marker in the emergency department (ED) has not yet been investigated.
Methods: We investigated sCD40L for the diagnosis of acute myocardial infarction or ischemic stroke in 1089 consecutive patients (525 males, 564 females; age, 17–98 years; median, 56 years) in an ED treating mainly adults with medical or neurologic emergencies. We used a research assay from Roche Diagnostics to measure sCD40L in heparinized plasma prepared from routinely drawn blood samples.
Results: Intraassay and interassay CVs in our laboratory ranged from 1.6%–4.2% and from 4.4%–4.9%, respectively. A multiple linear regression analysis revealed sCD40L concentration to be significantly associated with C-reactive protein concentration (P = 0.012) and platelet count (P < 0.001). In addition, a subgroup analysis revealed a significant association between smoking and sCD40L concentration (P = 0.006). All other tested variables, including discharge diagnosis, age, sex, and other laboratory variables, showed no significant associations.
Conclusions: In adults presenting to the ED, sCD40L is not useful as a diagnostic marker for acute cardiac, cerebrovascular ischemic, or thromboembolic events.
The following articles in journals at HighWire Press have cited this article:
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C. Antoniades, C. Bakogiannis, D. Tousoulis, A. S. Antonopoulos, and C. Stefanadis The CD40/CD40 ligand system: linking inflammation with atherothrombosis. J. Am. Coll. Cardiol., August 18, 2009; 54(8): 669 - 677. [Abstract] [Full Text] [PDF] |
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