US2013316377A1PendingUtilityA1
Methods for predicting and treating myocardial damage
Est. expirySep 21, 2030(~4.2 yrs left)· nominal 20-yr term from priority
A61K 9/0053G01N 2800/324G01N 33/92G01N 2800/56A61K 31/122A61K 45/06G01N 33/6887
45
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Claims
Abstract
A method for predicting myocardial damage in a subject having or at risk of cardiac disease includes determining a level of apolipoprotein AI (ApoAI) and a level of Coenzyme Q 10 (CoQ 10 ) in the subject and comparing the determined levels of ApoAI and CoQ 10 to control levels.
Claims
exact text as granted — not AI-modified1 . A method for predicting myocardial damage in a subject having or at risk of cardiac disease, the method comprising:
determining a level of apolipoprotein AI (ApoAI) in the subject; determining a level of Coenzyme Q 10 (CoQ 10 ) in the subject; comparing the determined levels of ApoA1 and CoQ 10 to control levels, wherein a decreased level of ApoAI and a decreased level of CoQ 10 compared to control levels are indicative of the subject having an increased risk of greater myocardial damage following a myocardial infarction.
2 . The method of claim 1 , further comprising the step of obtaining one or more bodily samples from the subject, the one or more bodily samples including CoQ 10 and ApoAI.
3 . The method of claim 2 , the one or more bodily samples comprising plasma.
4 . The method of claim 1 , wherein the level of ApoAI in the subject is determined using an ELISA assay.
5 . The method of claim 1 , wherein the level of CoQ 10 in the subject is determined using high-performance liquid chromatography.
6 . The method of claim 1 , wherein the myocardial damage comprises a ratio of an area of ischemic myocardial tissue to total area of myocardial tissue.
7 . The method of claim 1 , the control levels include normal levels of ApoA1 and CoQ10 in a population of apparently healthy subjects.
8 . The method of claim 1 , wherein the cardiac disease is selected from the group consisting of myocardial infarction, coronary artery disease, angina, atherosclerosis, aneurysm, congestive heart failure, left ventricular dysfunction, cerebrovascular disease, and cerebrovascular accident.
9 . A method of determining increased risk of greater myocardial damage in a subject having or at risk of cardiac disease, the method comprising:
determining a level of apolipoprotein AI (ApoAI) in the subject; determining a level of Coenzyme Q 10 (CoQ 10 ) in the subject; comparing the determined levels of ApoA1 and CoQ 10 to control levels, wherein a decreased level of ApoAI and a decreased level of CoQ 10 compared to control levels are indicative of the subject having an increased risk of greater myocardial damage following a myocardial infarction.
10 . The method of claim 9 , further comprising the step of obtaining one or more bodily samples from the subject, the one or more bodily samples including CoQ 10 and ApoAI.
11 . The method of claim 10 , the one or more bodily samples comprising plasma.
12 . The method of claim 9 , wherein the level of ApoAI in the subject is determined using an ELISA assay.
13 . The method of claim 9 , wherein the level of CoQ 10 in the subject is determined using high-performance liquid chromatography.
14 . The method of claim 9 , wherein the myocardial damage comprises a ratio of an area of ischemic myocardial tissue to total area of myocardial tissue.
15 . The method of claim 9 , the control levels include normal levels of ApoA1 and CoQ10 in a population of apparently healthy subjects.
16 . The method of claim 9 , wherein the cardiac disease is selected from the group consisting of myocardial infarction, coronary artery disease, angina, atherosclerosis, aneurysm, congestive heart failure, left ventricular dysfunction, cerebrovascular disease, and cerebrovascular accident.
17 . A method of determining increased risk of greater myocardial damage in a subject having or at risk of cardiac disease, the method comprising:
determining a level of HDL in the subject; determining a level of Coenzyme Q 10 (CoQ 10 ) in the subject; comparing the determined levels of ApoA1 and CoQ 10 to control levels, wherein a decreased level of ApoAI and a decreased level of CoQ 10 compared to control levels are indicative of the subject having an increased risk of greater myocardial damage following a myocardial infarction.
18 . The method of claim 17 , further comprising the step of obtaining one or more bodily samples from the subject, the one or more bodily samples including CoQ 10 and HDL.
19 . The method of claim 18 , the one or more bodily samples comprising plasma.
20 . The method of claim 17 , wherein the level of HDL in the subject is determined using a fluorometric assay.
21 . The method of claim 17 , wherein the level of CoQ 10 in the subject is determined using high-performance liquid chromatography.
22 . The method of claim 17 , wherein the myocardial damage comprises a ratio of an area of ischemic myocardial tissue to total area of myocardial tissue.
23 . The method of claim 17 , the control levels include normal levels of HDL and CoQ10 in a population of apparently healthy subjects.
24 . The method of claim 17 , wherein the cardiac disease is selected from the group consisting of myocardial infarction, coronary artery disease, angina, atherosclerosis, aneurysm, congestive heart failure, left ventricular dysfunction, cerebrovascular disease, and cerebrovascular accident.
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