This is a prospective randomized, double-blind placebo-controlled trial of 6 months' duration evaluating the effect of fenofibrate (200 mg/day) in females with polycystic ovary syndrome and mild hypertriglyceridemia. The investigators primary objective will be to determine whether fenofibrate will reduce hepatic adiposity as measured using MRI, and our secondary outcomes will be to delineate the impact of fenofibrate on biochemical or clinical parameters for insulin resistance, cardiovascular disease, and reproductive status.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
4
fenofibrate 200 mg daily for 6-months
Placebo match for 6 months
St. Joseph's Health Care
London, Ontario, Canada
Hepatic adiposity as assessed using MRI
Time frame: 6-months
Body composition using bioelectrical impedance analysis (BIA), anthropometry (skin-fold thickness measurement), and MRI
Time frame: 6-months
Insulin resistance using HOMA-IR
Time frame: 6 months
Biochemical parameters related to insulin resistance (adipocytokines, free fatty acids, 25-hydroxyvitamin D)
Time frame: 6 months
Traditional and non-traditional cardiovascular risk factors (lipids, apolipoproteins, fibrinogen, PAI-1, CRP)
Time frame: 6 months
Reproductive parameters (androgens, hirsutism)
Time frame: 6 months
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