Postprandial Fatty Acid Metabolism in Subjects With Lipoprotein Lipase Deficiency

Who May Qualify: - 8 healthy LPL-deficient individuals (LPLD subjects) with history of fasting TG \> 5 mmol/l and homozygote or compound heterozygote for a LPL-gene mutation; - 8 control subjects (fasting glucose \< 5.6, 2-hour post 75g OGTT glucose \< 7.8 mmol/l and HbA1c \< 5.8%; fasting TG \< 1.5 mmol/l); - age 18 to 75 yo; - To be willing and able to adhere to the specifications of the protocol; - To have signed an willing to sign a consent form document indicating that they understood the purpose Who Should NOT Join This Trial: - age \< 18 yo; - overt cardiovascular disease as assessed by medical history, physical exam, and abnormal ECG - Treatment with a fibrate, thiazolidinedione, beta-blocker or other drug known to affect lipid or carbohydrate metabolism (except statins, metformin, and other antihypertensive agents that can be safely interrupted); - Treatment with anti-hypertensive medication (only for LPL-deficient individuals); - presence of liver or renal disease; uncontrolled thyroid disorder; - previous diagnosis of heparin-induced thrombocytopenia; - Treatment with oral anticoagulation medication or platelet aggregation inhibiting drugs; - A history of major hemorrhagic event; - smoking (\>1 cigarette/day) and/or consumption of \>2 alcoholic beverages per day;; - Female of child-bearing potential who is pregnant, breast feeding or intends to become pregnant or pre-menopausal female with a positive serum pregnancy test at the time of enrollment. Always talk to your doctor about whether this trial is right for you.