2007
DOI: 10.1002/cyto.b.20377
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Flow cytometric assessment of platelet aspirin resistance using light scattering

Abstract: Background: A simple and reliable assay is needed for the prediction of the clinical efficacy of antiplatelet aspirin therapy. We have devised another method for the evaluation of platelet function and aspirin resistance (AR), via conventional flow cytometry (FCM).Methods: To devise an optimized protocol for the assessment of platelet AR, various analytic variables of FCM were investigated. Using this devised protocol, AR was assessed in healthy subjects as an example.Results: The protocol utilized herein is a… Show more

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Cited by 3 publications
(3 citation statements)
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References 22 publications
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“…Using this plot, the real‐time change of red cell numbers could be measured efficiently with only a single tube for comparison before and after DW spiking. We have also successfully applied this plot for the measurement of platelet aggregation (15). The time‐dependent plot is already widely used for many kinetic assays such as intracellular ionized calcium measurement (16).…”
Section: Discussionmentioning
confidence: 99%
“…Using this plot, the real‐time change of red cell numbers could be measured efficiently with only a single tube for comparison before and after DW spiking. We have also successfully applied this plot for the measurement of platelet aggregation (15). The time‐dependent plot is already widely used for many kinetic assays such as intracellular ionized calcium measurement (16).…”
Section: Discussionmentioning
confidence: 99%
“…While it is well known that autofluorescence generates false-positive monocytes [124], this aspect is neglected in platelet assays. Despite controversy regarding the relationship between CVD and platelet size, measured as mean platelet volume (MPV) or FS [97, 125, 126], it is well known that FS increases after platelet activation [127] and that large and small platelet subpopulations have different autofluorescence profiles [128] (Figure 1). Consequently, differences in autofluorescence in unstimulated and stimulated samples imply that stimulation indexes do not necessarily measure ROS production.…”
Section: Measurement Of Reactive Species In Leukocytes and Platelementioning
confidence: 99%
“…Samples were acquired on a BD FACSCalibur cytometer. In order to avoid artefacts in fluorescence signal due to platelets' dimension and aggregation [ 36 , 37 ], platelets were divided in two populations (R1 and R2) according to their FSC and CD61 staining. CD61 negative events, imputable to debris, were excluded from the analysis.…”
Section: Methodsmentioning
confidence: 99%