Methods for identifying patients with increased risk of an adverse cardiovascular event
View Patent ↗Methods, compositions and kits are disclosed for identifying patients with an increased risk of experiencing an adverse cardiovascular event where the patient is undergoing aspirin antiplatelet therapy. A platelet-containing sample from the patient is evaluated for platelet hyperactivity and platelet hyperactivity in the sample is related to the patient's risk of an adverse cardiovascular event. In some embodiments the evaluation for platelet hyperactivity is carried out by assessing the function of platelets in the sample using a high shear platelet function test.
1. A method for identifying a patient having an increased risk of an adverse cardiovascular event wherein the patient is undergoing aspirin antiplatelet therapy, said method comprising:
(a) evaluating a platelet-containing sample from the patient for platelet hyperactivity wherein the patient is aspirin sensitive, which is defined as a patient for whom aspirin therapy is considered effective as determined by an optical aggregation method utilizing arachidonic acid-induced and ADP-induced platelet aggregometry and
(b) relating platelet hyperactivity in the sample to the patient's risk of an adverse cardiovascular event.
2. A method according to claim 1 wherein the evaluating of step (a) is carried out by assessing the function of platelets in the sample using a high shear platelet function test.
3. A method according to claim 1 wherein platelet function is assessed by a high shear platelet function test using a platelet aggregation stimulator.
4. A method according to claim 3 wherein the platelet aggregation stimulator is selected from the group consisting of collagen, ristocetin, arachidonic acid, serotonin, adenosine-5′-diphosphate, epinephrine, and thrombin and combinations thereof.
5. A method according to claim 4 wherein the platelet aggregation stimulator is collagen and adenosine-5′-diphosphate.
6. A method according to claim 1 wherein the sample is drawn under vacuum through a capillary so that it contacts a membrane comprising an aperture and platelets in the sample are activated by means of shear force and the time to formation of a platelet plug that blocks the aperture is measured and related to the increased risk of an adverse cardiovascular event in the patient.
7. A method according to claim 6 wherein the membrane comprises a platelet aggregation stimulator.
8. A method according to claim 7 wherein the platelet aggregation stimulator is selected from the group consisting of collagen, ristocetin, arachidonic acid, serotonin, adenosine-5′-diphosphate, epinephrine, and thrombin and combinations thereof.
9. A method according to claim 7 wherein the platelet aggregation stimulator is collagen and adenosine-5′-diphosphate.
10. A method according to claim 1 wherein the platelet-containing sample is whole blood.
11. A method for assessing the risk of an adverse cardiovascular event in a patient undergoing antiplatelet aspirin therapy, said method comprising:
(a) drawing a platelet-containing sample from the patient under vacuum through a capillary so that it contacts a membrane comprising an aperture and platelets in the sample are activated by means of shear force, wherein the membrane comprises a platelet aggregation stimulator and wherein the patient is aspirin sensitive, which is defined as a patient for whom aspirin therapy is considered effective as determined by an optical aggregation method utilizing arachidonic acid-induced and ADP-induced platelet aggregometry,
(b) measuring the time to formation of a platelet plug that blocks the aperture of the membrane, and
(c) relating the time to formation of the platelet plug to the patient's risk of an adverse cardiovascular event.
12. A method according to claim 11 wherein the platelet aggregation stimulator is selected from the group consisting of collagen, ristocetin, arachidonic acid, serotonin, adenosine-5′-diphosphate, epinephrine, and thrombin and combinations thereof.
13. A method according to claim 11 wherein the platelet aggregation stimulator is collagen and adenosine-5′-diphosphate.
14. A method according to claim 11 wherein the platelet-containing sample is whole blood.
15. A method according to claim 11 wherein the time to formation of a platelet plug is compared to a predetermined time and a time to formation of a platelet plug less than the predetermined time is indicative of an increased risk of the patient for an adverse cardiovascular event.
16. A method for assessing the risk of an adverse cardiovascular event in a patient undergoing antiplatelet aspirin therapy, said method comprising:
(a) drawing a whole blood sample from the patient under vacuum through a capillary so that it contacts a membrane comprising an aperture and platelets in the sample are activated by means of shear force, wherein the membrane comprises a platelet aggregation stimulator and wherein the patient is aspirin sensitive, which is defined as a patient for whom aspirin therapy is considered effective as determined by an optical aggregation method utilizing arachidonic acid-induced and ADP-induced platelet aggregometry,
(b) measuring the time to formation of a platelet plug that blocks the aperture of the membrane, and
(c) relating the time to formation of the platelet plug to the patient's risk of an adverse cardiovascular event wherein the time to formation of a platelet plug is compared to a predetermined time and a time to formation of a platelet plug less than the predetermined time is indicative of an increased risk of the patient for an adverse cardiovascular event.
17. A method according to claim 16 wherein the platelet aggregation stimulator is selected from the group consisting of collagen, ristocetin, arachidonic acid, serotonin, adenosine-5′-diphosphate, epinephrine, and thrombin and combinations thereof.
18. A method according to claim 16 wherein the platelet aggregation stimulator is collagen and adenosine-5′-diphosphate.