Compositions and methods for lowering triglycerides without raising LDL-C levels in a subject on concomitant statin therapy
View Patent ↗In various embodiments, the present invention provides compositions and methods for treating and/or preventing cardiovascular-related diseases in subject in need thereof.
1. A method of lowering triglycerides in a subject on statin therapy having baseline fasting triglycerides of about 200 mg/dl to less than 500 mg/dl and a baseline fasting high density lipoprotein cholesterol (“HDL-C”) level of about 10 mg/dl to about 100 mg/dl, the method comprising determining a baseline fasting triglyceride level, a baseline fasting HDL-C level, and a baseline fasting Apolipoprotein B (“Apo B”) level associated with the subject; and thereafter administering to the subject about 2 grams or about 4 grams per day of ethyl eicosapentaenoate, wherein after the administering, an Apo B level associated with the subject decreases by at least about 5% compared to a second subject who has received statin therapy but not the ethyl eicosapentaenoate.
2. The method of claim 1 further comprising determining a baseline fasting low density lipoprotein cholesterol (“LDL-C”) level associated with the subject before the administering, wherein an LDL-C level associated with the subject after the administering is not increased compared to the baseline fasting LDL-C level.
3. The method of claim 1 , wherein the subject is administered about 2 grams per day of ethyl eicosapentaenoate, and wherein the triglycerides are lowered by about 10% compared to a second subject who has received statin therapy but not the ethyl eicosapentaenoate.
4. The method of claim 2 , wherein the subject is administered about 2 grams per day of ethyl eicosapentaenoate, and wherein the triglycerides are lowered by about 10% compared to a second subject who has received statin therapy but not the ethyl eicosapentaenoate.
5. The method of claim 1 , wherein the subject is administered about 4 grams per day of ethyl eicosapentaenoate, and wherein the triglycerides are lowered by about 21% compared to a second subject who has received statin therapy but not the ethyl eicosapentaenoate.
6. The method of claim 2 , wherein the subject is administered about 4 grams per day of ethyl eicosapentaenoate, and wherein the triglycerides are lowered by about 21% compared to a second subject who has received statin therapy but not the ethyl eicosapentaenoate.
7. The method of claim 1 farther comprising determining a baseline fasting very low density lipoprotein cholesterol (“VLDL-C”) level associated with the subject, wherein after the administering an VLDL-C level associated with the subject is lower than the baseline fasting VLDL-C level compared to a second subject who has received statin therapy but not the ethyl eicosapentaenoate.
8. The teethed of claim 1 further comprising determining a baseline fasting lipoprotein-associated phospholipase A2 (“LP-PLA 2 ”) level associated with the subject, wherein after the administering an LP-PLA 2 level associated with the subject is lower than the baseline fasting LP-PLA 2 level compared to a second subject who has received statin therapy but not the ethyl eicosapentaenoate.
9. The method of claim 1 further comprising determining baseline fasting levels of low density lipoprotein cholesterol “(LDL-C”), very low density lipoprotein cholesterol (“VLDL-C”) and lipoprotein-associated phospholipase A2 (“LP-PLA 2 ”) associated with the subject, wherein after the administering levels of LDL-C, Apo B, VLDL-C and Lp-PLA 2 associated with the subject are lower than the baseline fasting levels compared to a second subject who has received statin therapy but not the ethyl eicosapentaenoate.
10. The method of claim 9 , wherein the subject receives about 2 grams of ethyl eicosapentaenoate per day.
11. The method of claim 9 , wherein the subject receives about 4 grams of ethyl eicosapentaenoate per day.
12. The method of claim 2 , wherein the subject has a baseline fasting LDL-C level of about 82 mg/dl.
13. The method of claim 1 , wherein the subject has a baseline fasting Apo B level of about 21.7 mg/dl or about 227 mg/dl.
14. The method of claim 7 , wherein the subject has a baseline fasting VLDL-C level of about 225 mg/dl or about 233 mg/dl.
15. The method of claim 8 , wherein the subject has a baseline fasting Lp-PLA 2 level of about 217 mg/dl or about 224 mg/dl.
16. The method of claim 9 , wherein the subject has:
a baseline fasting LDL-C level of about 82 mg/dl;
the baseline fasting Apo B level of about 217 mg/dl or about 227 mg/dl;
a baseline fasting VLDL-C level of about 225 mg/dl or about 233 mg/dl; and
a baseline fasting Lp-PLA 2 level of about 217 mg/dl or about 224 mg/dl.