Increased plasma levels of soluble CD40 ligand correlate with platelet activation markers and underline the need for standardized pre-analytical conditions

To investigate whether sCD40L dosage might represent a useful tool to explore in vivo platelet function. sCD40L and sP-selectin levels and light transmission aggregometry (LTA) were analyzed in 69 healthy donors. Immunoassays were performed on platelet-depleted citrate plasma samples. The effects of...

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Published inClinical biochemistry Vol. 43; no. 7; pp. 666 - 670
Main Authors Riondino, Silvia, Martini, Francesca, La Farina, Francesca, Spila, Antonella, Guadagni, Fiorella, Ferroni, Patrizia
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier Inc 01.05.2010
Elsevier
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Summary:To investigate whether sCD40L dosage might represent a useful tool to explore in vivo platelet function. sCD40L and sP-selectin levels and light transmission aggregometry (LTA) were analyzed in 69 healthy donors. Immunoassays were performed on platelet-depleted citrate plasma samples. The effects of in vitro aspirin treatment on the release of sCD40L were investigated in 15 subjects following platelet stimulation. The effects of a 1-month therapeutic course of low-dose aspirin on sP-selectin and sCD40L levels were also investigated. A significant correlation was observed between sCD40L and sP-selectin ( p < 0.01). In vitro aspirin treatment remarkably decreased sCD40L levels following platelet activation by exogenous agonists. sCD40L directly correlated with LTA (Rho = 0.62, p < 0.0001). In vivo aspirin treatment significantly reduced both sP-selectin and sCD40L levels (both p < 0.01) in a direct correlation (Rho = 0.66, p < 0.05). Citrated plasma samples reflect sCD40L released from platelets, thus yielding the most valid estimates of in vivo circulating levels of this platelet activation markers.
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ISSN:0009-9120
1873-2933
DOI:10.1016/j.clinbiochem.2009.12.021