Key result
Canine malignancy is linked to faster, stronger platelet aggregation and higher ATP secretion versus controls.
Why the study?
The platelet function characteristics in dogs with malignancies compared to healthy controls were not well defined.
Case-Control (n=83)
p-value: p=<.05
May indicate heightened thrombotic risk in canine malignancy; hypothesis-generating and requires in vivo confirmation.
In vitro platelet aggregometry was performed on whole blood samples from 59 dogs with malignancies and 24 control dogs. Three reagents were used for the aggregation studies: collagen, arachidonic acid, and adenosine diphosphate (ADP). The parameters measured to evaluate response to collagen included delay in the aggregation response, slope of the aggregation curve, maximum aggregation, and adenosine triphosphate (ATP) secretion. The platelets of dogs with malignancies exhibited significantly (P < .05) shorter delays in the aggregation response, higher maximum aggregation, and higher ATP secretion when compared to control dogs. For the weaker reagents, ADP and arachidonic acid, the lowest concentration resulting in aggregation was determined. Platelets of dogs with malignancies tended to aggregate in response to lower concentrations of ADP than did those of controls (P < .05). The response of platelets to the concentrations of arachidonic acid employed in this study was poor, with few samples achieving measurable aggregation. The findings of this study suggest that dogs with malignancies have hyperaggregable platelets.
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McNiel et al. (1997) conducted a case-control in Malignancies (n=83). Malignancies vs. Control dogs was evaluated on Platelet aggregation response (delay, maximum aggregation, ATP secretion) (p=<.05). Dogs with malignancies exhibited significantly shorter delays in aggregation response, higher maximum aggregation, and higher ATP secretion compared to control dogs (P < .05).
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