Methods of treating hypertriglyceridemia
View Patent ↗In various embodiments, the present invention provides methods of treating and/or preventing cardiovascular-related disease and, in particular, a method of blood lipid therapy comprising administering to a subject in need thereof a pharmaceutical composition comprising eicosapentaenoic acid or a derivative thereof.
1. A method of reducing high-sensitivity C-reactive protein and triglycerides in a subject having a fasting baseline triglyceride level of 500 mg/dl to about 1500 mg/dl, who does not receive a concurrent lipid altering therapy, comprising administering orally to the subject about 4 g per day of a pharmaceutical composition comprising at least about 96% by weight, ethyl eicosapentaenoate (ethyl-EPA) and substantially no docosahexaenoic acid (DHA) or its esters for a period of at least 12 weeks to effect a reduction in high-sensitivity C-reactive protein and triglycerides in the subject compared to a group of subjects having a median fasting baseline triglyceride level of 500 mg/dl to about 1500 mg/dl, who do not receive a concurrent lipid altering therapy, and who have not received the pharmaceutical composition.
2. The method of claim 1 , wherein the subject has a fasting baseline triglyceride level of 750 mg/dl to about 1500 2000 mg/dl.
3. The method of claim 1 , wherein the subject is diabetic.
4. The method of claim 1 comprising administering the pharmaceutical composition to the subject daily for a period of at least 12 weeks to effect a reduction in high-sensitivity C-reactive protein of at least about 10% compared to the group of subjects.
5. The method of claim 1 comprising administering the pharmaceutical composition to the subject daily for a period of at least 12 weeks to effect a reduction in high-sensitivity C-reactive protein of at least about 20% compared to the group of subjects.
6. The method of claim 5 wherein the subject exhibits at least a 35% reduction in fasting triglycerides and no statistically significant increase in LDL-C compared to a baseline triglyceride and LDL-C level prior to initial administration of the pharmaceutical composition.
7. The method of claim 1 wherein the subject exhibits at least a 10% reduction in high-sensitivity C-reactive protein after the period of at least 12 weeks compared to a baseline high-sensitivity C-reactive protein level prior to initial administration of the pharmaceutical composition.
8. The method of claim 1 wherein the subject exhibits at least a 20% reduction in high-sensitivity C-reactive protein after the period of at least 12 weeks compared to a baseline high-sensitivity C-reactive protein level prior to initial administration of the pharmaceutical composition.
9. The method of claim 1 , wherein comprising administering to effect a reduction in apolipoprotein B without increasing LDL C compared to the group of subjects.
10. The method of claim 1 , wherein about one gram of the pharmaceutical composition is present in each of four capsules.
11. The method of claim 10 , wherein 2 of the capsules are administered to the subject twice each day.
12. The method of claim 1 , wherein the subject and the second subject consume a Western diet.
13. The method of claim 1 , wherein the concomitant lipid-altering therapy is a statin.
14. The method of claim 1 comprising administering the pharmaceutical composition to the subject to effect a reduction in triglycerides of at least 15% in the subject compared to the group of subjects.