Effect of Fish Oil Enriched In Omega-11 Fatty Acid On Lipoprotein Metabolism In Adults

Serum cholesterol is transported by lipoproteins, such as very low-density lipoprotein (VLDL), low-density lipoproteins (LDL) and high-density lipoproteins (HDL), which vary in their relationship to cardiovascular disease risk. LDL, for example, is proatherogenic, whereas HDL is cardio-protective. Long-chain monounsaturated fatty acids (LCMUFA), fatty acids over 18 carbons in length with a single double bond, have been shown in mice to decrease proatherogenic lipoproteins, such as LDL, and reduce atherosclerosis. This study will test the hypothesis that LCMUFA supplementation in humans will favorably alter the lipoprotein lipid profile in regard to cardiovascular disease risk. In addition, we will assess other parameters related to lipoprotein composition and function, as well as other biomarkers related to coagulation and inflammation, which have previously been shown to be affected by supplementation with omega-3 fatty acids.

This clinical research project is designed as a pilot, randomized, double-blinded, crossover study that will investigate the effect of a fish oil enriched with LCMUFA on lipoprotein metabolism. Subjects will receive control fish oil enriched in oleic acid, a monounsaturated fatty acid (C18:1), or a fish oil supplement produced from Saury fish (rich in LCMUFA) for approximately 8-10 weeks, with a wash out period of 8-10 weeks between the two arms of the study. The study consists of 4 outpatient visits when laboratory or research samples and CAVI tests will be performed. A 7-day food diary, pill count, and red cell membrane fatty acid levels will be monitored to assess compliance.

• INCLUSION CRITERIA:
• Male and female participants 18 years of age or above.
• Subject must be healthy, with no known history of cardiovascular disease.
• Pre-menopausal or women of childbearing potential must be non-lactating and using an effective form of birth control during the course of the study.
• Subject understands protocol and provides written, informed consent in addition to a willingness to comply with specified follow-up evaluations.

Exclusion criteria

• Pregnancy, planned pregnancy (within the study period) or women currently breastfeeding.
• Subjects with weight changes greater than 20% over the past 3 months.
• Subjects planning a significant change in diet or exercise levels.
• Subjects already consuming more than 1.5 g per day of eicosapentaenoic acid (EPA) or docosahexaenoic acid (DHA) in any form.
• Known sensitivity or allergy to fish, shellfish or omega-3 fatty acids supplements
• Subjects with known bleeding disorders (for example, Hemophilia)
• Subjects previously diagnosed with atrial fibrillation
• Subjects with clinically diagnosed hepatic disease (including but not limited to auto immune disease, hepatitis and cirrhosis)
• Subjects with chronic diarrhea, gastric bypass or lap-band procedures, ostomies, bowel motility problems, or other conditions that could affect intestinal fat absorption
• Subjects with any acute and life-threatening condition, such as prior sudden cardiac arrest, acute myocardial infarction (last three months), stroke, embolism
• Liver enzymes (aspartate aminotransferase (AST) or alanine aminotransferase (ALT)) levels above 3x upper limit of normal
• Subjects with a thyroid-stimulating hormone (TSH) greater than 1.5x upper limits of normal (ULN) or clinical evidence of hypo or hyperthyroidism
• Subjects taking supplements or medications that affect lipoproteins for at least the past 8 weeks, such as fish oil supplements, bile-acid sequestrants, plant sterol supplements, fibrates, statins or Niacin.
• Subjects with hemoglobin <10g/dL
• Subject with platelet counts <60x103/microliter
• Subjects with uncontrolled hypertension (resting blood pressure > 160 mmHg systolic and /or > 100 mm Hg diastolic)
• Subject with uncontrolled diabetes (hemoglobin A1c (HbA1c) greater than or equal to 10)
• Subjects who consume excessive alcohol (binge drinking on 5 or more days in the past month)
• Subject participating in other clinical studies and/or receiving other investigational drug products prior to randomization
• Subject taking PCSK9 inhibitors within 8 weeks prior to enrollment
• Subjects being treated with tamoxifen, estrogens, or progestins that have not been stable for >4 weeks.
• Subjects initiating new medications or patients on multiple medications may also be excluded according to investigator discretion
• Anticipated surgery during the study period
• Blood donation in the last 2 weeks or planned blood donation during the study
• Subjects requiring regular transfusions for any reason
• Subjects may also be excluded for any reason that may compromise their safety or the accuracy of research data.