Composition and Treatment Methods for Coronary Artery Disease
The present disclosure demonstrates that cholesterol-free discoidal reconstituted HDL (R-HDL), phosphatidyl-choline (PC) and PC liposomes effectively released cholesterol from ICP. Native HDL and its apolipoproteins were not able to release cholesterol from ICP. The release of ICP cholesterol by R-HDL was dose-dependent and accompanied by the transfer of >8× more PC in the reverse direction (i.e., from R-HDL to ICP), resulting in a marked enrichment of ICP with PC. The enrichment of ICP with PC resulted in the dissolution of cholesterol crystals on ICP and allowed the removal of ICP cholesterol by apo HDL and plasma. The present disclosure provides a method of treatment for removal of cholesterol from ICP in vivo and compositions for use in such method of treatment. Such methods may be used in the treatment and/or prevention of atherosclerosis, coronary artery disease, and related disease states and conditions.
1 . A method for reducing the volume of a plaque in a subject, said method comprising the step of administering to said subject a therapeutically effective amount of a lipid composition comprising phosphatidylcholine, said phosphatidylcholine being dimyristoyl phosphatidylcholine or egg phosphatidylcholine, whereby at least a portion of said phosphatidylcholine is transferred from said lipid composition to said plaque.
2 . A method for increasing the stability of a plaque in a subject, said method comprising the step of administering to said subject a therapeutically effective amount of a lipid composition comprising phosphatidylcholine, said phosphatidylcholine being dimyristoyl phosphatidylcholine or egg phosphatidylcholine, whereby at least a portion of said phosphatidylcholine is transferred from said lipid composition to said plaque.
3 . A method of increasing the percentage of a phospholipid component in a plaque in a subject, said method comprising the step of administering to said subject a therapeutically effective amount of a lipid composition comprising phosphatidylcholine, said phosphatidylcholine being dimyristoyl phosphatidylcholine or egg phosphatidylcholine, whereby at least a portion of said phosphatidylcholine is transferred from said lipid composition to said plaque.
4 . A method for enriching a plaque in a subject with phosphatidylcholine, said method comprising the step of administering to said subject a therapeutically effective amount of a lipid composition comprising phosphatidylcholine, said phosphatidylcholine being dimyristoyl phosphatidylcholine or egg phosphatidylcholine, whereby at least a portion of said phosphatidylcholine is transferred from said lipid composition to said plaque.
5 . A method for decreasing a free cholesterol to phospholipid ratio in a plaque from a subject, said method comprising the step of administering to said subject a therapeutically effective amount of a lipid composition comprising phosphatidylcholine, said phosphatidylcholine being dimyristoyl phosphatidylcholine or egg phosphatidylcholine, whereby at least a portion of said phosphatidylcholine is transferred from said lipid composition to said plaque.
6 . (canceled)
7 . (canceled)
8 . The method of any of claims 1 - 5 where said lipid composition further comprises a protein component.
9 . The method of claim 9 where said protein component is an apolipoprotein.
10 . The method of claim 10 where said apolipoprotein is apolipoprotein A1.
11 . The method of claim 10 where said apolipoprotein to phosphatidylcholine ration is from about 1:1 to about 1:8.
12 . The method of any of claims 1 - 5 where said lipid composition is a high density lipoprotein.
13 . (canceled)
14 . (canceled)
15 . The method of any of claims 1 - 5 where said lipid composition is a liposome.
16 . (canceled)
17 . (canceled)
18 . The method of any of claims 1 - 5 where said subject is a human.
19 . A method for releasing cholesterol from a plaque in a subject, said method comprising the steps of administering to said subject a therapeutically effective amount of a lipid composition comprising phosphatidylcholine, said phosphatidylcholine being dimyristoyl phosphatidylcholine or egg phosphatidylcholine, whereby at least a portion of said phosphatidylcholine is transferred from said lipid composition to said plaque, and further administering to said subject a therapeutically effective amount of a cholesterol mobilizing agent whereby at least a portion of the cholesterol component of the plaque is transferred from said plaque to said cholesterol mobilizing agent.
20 . The method of claim 19 where the cholesterol mobilizing agent is fresh plasma or a second lipid composition not comprising phosphatidylcholine.
21 . The method of claim 19 where said second lipid composition comprises at least one protein.
22 . The method of claim 21 where said at least one protein is an apolipoprotein.
23 . The method of claim 22 where said apolipoprotein is apolipoprotein A1.
24 . The method of claim 23 where said apolipoprotein to phospholipid ratio is from about 1:1 to about 1:8.
25 . (canceled)
26 . (canceled)
27 . The method of any of claims 19 - 24 where said lipid composition is a high density lipoprotein.
28 . (canceled)
29 . (canceled)
30 . The method of any of claims 19 - 24 where said lipid composition is a liposome.
31 . (canceled)
32 . (canceled)
33 . The method of any of claims 19 - 24 where said subject is a human.
34 . A method for releasing cholesterol from a plaque in a subject, said method comprising altering the lipid composition of said plaque in the subject by administering to said subject a therapeutically effective amount of a lipid composition comprising phosphatidylcholine, whereby at least a portion of said phosphatidylcholine is transferred from said lipid composition comprising phosphatidylcholine to said plaque, and further administering to said subject a therapeutically effective amount of a cholesterol mobilizing agent whereby at least a portion of the cholesterol component of the plaque is transferred from said plaque to said cholesterol mobilizing agent.
35 . The method of claim 34 where said phosphatidylcholine is dimyristoyl phosphatidylcholine or egg phosphatidylcholine.
36 . The method of claim 34 where the cholesterol mobilizing agent is fresh plasma or a second lipid composition not comprising phosphatidylcholine.
37 . The method of claim 34 where said second lipid composition comprises at least one protein.
38 . The method of claim 37 where said at least one protein is an apolipoprotein.
39 . The method of claim 37 where said apolipoprotein is apolipoprotein A1.
40 . The method of claim 39 where said apolipoprotein to phospholipid ratio is from about 1:1 to about 1:8.
41 . A method for increasing the stability of a plaque in a subject or regressing said plaque said subject, said method comprising altering the lipid composition of said plaque in the subject by administering to said subject a therapeutically effective amount of a lipid composition, whereby at least a portion of said phosphatidylcholine is transferred from said lipid composition to said plaque.
42 . The method of claim 41 where said phosphatidylcholine is dimyristoyl phosphatidylcholine or egg phosphatidylcholine.
43 . The method of claim 41 where said lipid composition is a high density lipoprotein or a liposome.
44 . The method of claim 41 where said lipid composition further comprises a protein component.
45 . The method of claim 44 where said protein component is an apolipoprotein.
46 . The method of claim 44 where said apolipoprotein is apolipoprotein A1.
47 . The method of claim 46 where said apolipoprotein to phosphatidylcholine ration is from about 1:1 to about 1:8.