IP Library Patent Application 14540749
Patent Application
App. No. 14/540,749

METHODS FOR TREATMENT OF CORONARY HEART DISEASE EVENTS BASED ON LIPOPROTEIN-ASSOCIATED PHOSPHOLIPASE A2 ACTIVITY

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Patent No.
US None
App. No.
14/540,749
Abstract

Methods of treating coronary heart disease (CHD) events by measuring Lp-PLA2 activity are described herein. Described herein are methods that compare Lp-PLA2 activity levels to a binary cut point to guide clinical diagnosis and treatment of CHD. The methods described herein provide robust treatment of patients regardless of race or gender, and may allow the simplification of complex treatment decisions and enhance patient care.

Claims (42)

1 . A method of treating a patient for coronary heart disease (CHD), the method comprising:

performing a test providing the amount of lipoprotein-associated phospholipase A2 (Lp-PLA2) activity in a patient sample, wherein the test comprises:

contacting a portion of the patient sample with an artificial substrate for Lp-PLA2 to enzymatically degrade the substrate,

detecting a signal that is proportional to the degradation of the artificial substrate for Lp-PLA2, and

determining an amount of Lp-PLA2 activity based on the signal;

determining that the amount of Lp-PLA2 activity is at or above a cut point when the amount of Lp-PLA2 activity is greater than or equal to a cut point comprising an amount equivalent to a measurement of Lp-PLA2 activity in serum or plasma value of 225 nmol/min/mL; and

treating the patient for CHD when the amount of Lp-PLA2 activity in the patient sample is at or above the cut point.

2 . The method of claim 1 , further comprising indicating that the amount of Lp-PLA2 activity is at or above the cut point when the amount of Lp-PLA2 activity in the patient sample is greater than or equal to an amount equivalent to the cut point.

3 . The method of claim 1 , wherein treating comprises administering an agent to treat CHD.

4 . The method of claim 2 , wherein administering comprises administering one or more medications selected from the group consisting of: an Lp-PLA2 inhibitor, an anti-inflammatory agent, an anti-thrombotic agent, an anti-platelet agent, a fibrinolytic agent, a lipid reducing agent, a direct thrombin inhibitor, a glycoprotein II b/IIIa receptor inhibitor, an agent that binds to cellular adhesion molecules and inhibits the ability of white blood cells to attach, an aldosterone antagonist, an angiotensin-converting enzyme (ACE) inhibitor, am angiotensin-receptor blocker (ARB), aspirin, a beta blocker, digoxin, a diuretic, an inotrope, digitalis, hydralazine, nitrates, statins, and warfarin.

5 . (canceled)

6 . The method of claim 1 , wherein treating the patient for CHD comprises treating the patient of any race or gender when the amount of Lp-PLA2 activity in the patient sample is greater than or equal to an amount equivalent to an Lp-PLA2 activity of 225 nmol/min/mL.

7 . A method of treating a patient for coronary heart disease (CHD), the method comprising:

performing a test providing the amount of Lp-PLA2 activity from a patient sample, wherein the test comprises:

contacting a portion of the patient sample with an artificial substrate for lipoprotein-associated phospholipase A2 (Lp-PLA2) to enzymatically degrade the substrate,

detecting a signal that is proportional to the degradation of the artificial substrate for Lp-PLA2, and

determining an amount of Lp-PLA2 activity based on the signal;

determining that the amount of Lp-PLA2 activity is at or above a cut point when the amount of Lp-PLA2 activity in the patient sample is greater than or equal to a cut point comprising an amount equivalent to a measurement of Lp-PLA2 activity in serum or plasma value of 225 nmol/min/mL; and

administering an agent to treat coronary heart disease when the amount of Lp-PLA2 activity in the patient sample is at or above the cut point.

8 . The method of claim 7 , further comprising indicating that the amount of Lp-PLA2 activity is at or above the cut point when the amount of Lp-PLA2 activity in the patient sample is greater than or equal to an amount equivalent to the cut point of 225 nmol/min/mL.

9 . The method of claim 7 , wherein administering comprises administering the agent to treat coronary heart disease when the amount of active Lp-PLA2 in the patient sample is greater than or equal to 220 ng/mL.

10 . The method of claim 7 , wherein administering comprises administering one or more medications selected from the group consisting of: an Lp-PLA2 inhibitor, an anti-inflammatory agent, an anti-thrombotic agent, an anti-platelet agent, a fibrinolytic agent, a lipid reducing agent, a direct thrombin inhibitor, a glycoprotein II b/IIIa receptor inhibitor, an agent that binds to cellular adhesion molecules and inhibits the ability of white blood cells to attach, an aldosterone antagonist, an angiotensin-converting enzyme (ACE) inhibitor, am angiotensin-receptor blocker (ARB), aspirin, a beta blocker, digoxin, a diuretic, an inotrope, digitalis, hydralazine, nitrates, statins, and warfarin.

11 . The method of claim 7 , wherein administering the agent comprises administering the agent to the patient, wherein the patient is of any race or gender when the amount of Lp-PLA2 activity in the patient sample is greater than or equal to an amount equivalent to 225 nmol/min/mL using a substrate of 1-myristoyl-2-(4-nitrophenyl succinyl) phosphatidylcholine.

12 . A method of treating a patient for coronary heart disease (CHD), the method comprising:

contacting a portion of a sample from the patient with an artificial substrate for lipoprotein-associated phospholipase A2 (Lp-PLA2) comprising 1-myristoyl-2-(p-nitrophenylsuccinyl) phosphatidylcholine, to enzymatically degrade the substrate;

detecting a signal that is proportional to the degradation of the artificial substrate for Lp-PLA2;

calculating an amount of Lp-PLA2 activity based on the signal;

determining that the amount of Lp-PLA2 activity is at or above a cut point when the amount of Lp-PLA2 activity in the patient sample is greater than or equal to a cut point comprising an amount equivalent to a measurement of Lp-PLA2 activity in serum or plasma value of 225 nmol/min/mL; and

treating the patient for CHD when the amount of Lp-PLA2 activity in the patient sample is greater than or equal to the cut point.

13 . The method of claim 12 , further comprising indicating that the amount of Lp-PLA2 activity is at or above the cut point.

14 . The method of claim 12 , wherein treating comprises instructing a physician that the patient is at risk for coronary heart disease so that the physician may administer to the patient a therapy for CHD.

15 . The method of claim 12 , wherein treating comprises instructing a physician that the patient's Lp-PLA2 activity is greater than or equal to 225 nmol/min/mL and the patient is at risk for coronary heart disease so that the physician may administer to the patient a therapy for CHD.

16 . The method of claim 12 , wherein treating comprises administering an agent to treat CHD.

17 . The method of claim 12 , wherein treating comprises administering one or more medications selected from the group consisting of: an Lp-PLA2 inhibitor, an anti-inflammatory agent, an anti-thrombotic agent, an anti-platelet agent, a fibrinolytic agent, a lipid reducing agent, a direct thrombin inhibitor, a glycoprotein II b/IIIa receptor inhibitor, an agent that binds to cellular adhesion molecules and inhibits the ability of white blood cells to attach, an aldosterone antagonist, an angiotensin-converting enzyme (ACE) inhibitor, am angiotensin-receptor blocker (ARB), aspirin, a beta blocker, digoxin, a diuretic, an inotrope, digitalis, hydralazine, nitrates, statins, and warfarin.

18 . A method of treating a patient of any race for coronary heart disease (CHD), the method comprising:

contacting a portion of a sample from the patient with an artificial substrate for lipoprotein-associated phospholipase A2 (Lp-PLA2) comprising 1-myristoyl-2-(p-nitrophenylsuccinyl) phosphatidylcholine, to enzymatically degrade the substrate;

detecting a signal that is proportional to the degradation of the artificial substrate for Lp-PLA2;

calculating an amount of Lp-PLA2 activity based on the signal;

determining that the amount of Lp-PLA2 activity is at or above a cut point when the amount of Lp-PLA2 activity in the patient sample is greater than or equal to a cut point comprising an amount equivalent to a measurement of Lp-PLA2 activity in serum or plasma value of 225 nmol/min/mL; and

administering an agent to the patient to treat coronary heart disease when the amount of Lp-PLA2 activity in the patient sample is at or above the cut point.

19 . The method of claims 18 , wherein administering comprising instructing a medical professional to administer an agent to the patient the patient to treat CHD.

20 . The method of claim 18 , wherein administering comprises administering one or more medications selected from the group consisting of: an Lp-PLA2 inhibitor, an anti-inflammatory agent, an anti-thrombotic agent, an anti-platelet agent, a fibrinolytic agent, a lipid reducing agent, a direct thrombin inhibitor, a glycoprotein II b/IIIa receptor inhibitor, an agent that binds to cellular adhesion molecules and inhibits the ability of white blood cells to attach, an aldosterone antagonist, an angiotensin-converting enzyme (ACE) inhibitor, am angiotensin-receptor blocker (ARB), aspirin, a beta blocker, digoxin, a diuretic, an inotrope, digitalis, hydralazine, nitrates, statins, and warfarin.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 7, 2017
From: GENERAL ATOMICS
To: DIAZYME LABORATORIES, INC.
Reel/Frame 041651/0661 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 4, 2017
From: DIADEXUS, INC.
To: GENERAL ATOMICS
Reel/Frame 041245/0899 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 28, 2016
From: ARENSDORF, PATRICK ALFRED; CERELLI, MARY JANE; GERWIEN JR., ROBERT WILLIAM; ZYCHLINSKY, EMI
To: DIADEXUS, INC.
Reel/Frame 040791/0656 →
CHANGE OF NAME Recorded Dec 28, 2016
From: DIADEXUS, INC.
To: DIADEXUS, INC.
Reel/Frame 040791/0732 →