(TG), increased total and LDL-cholesterol concentrations and decreased HDL-cholesterol concentration, is an important risk factor for cardiovascular disease. Premenopausal women have a less atherogenic plasma lipid profile and a lower risk of cardiovascular disease than men, but this female advantage disappears after menopause. This suggests that female sex steroids affect lipoprotein metabolism. The impact of variations in the availability of ovarian hormones during the menstrual cycle on lipoprotein metabolism is not known. We therefore investigated whether very-low-density lipoprotein (VLDL)-TG and VLDL-apolipoprotein B-100 (apoB-100) kinetics are different during the follicular (FP) and luteal phases (LP) of the menstrual cycle. We studied seven healthy, premenopausal women (age 27 Ϯ 2 yr, BMI 25 Ϯ 2 kg/m 2 ) once during FP and once during LP. We measured VLDL-TG, VLDL-apoB-100, and plasma free fatty acid (FFA) kinetics by using stable isotope-labeled tracers, VLDL subclass profile by nuclear magnetic resonance spectroscopy, whole body fat oxidation by indirect calorimetry, and the plasma concentrations of lipoprotein lipase (LPL) and hepatic lipase (HL) by ELISA. VLDL-TG and VLDLapoB-100 concentrations in plasma, VLDL-TG and VLDL-apoB-100 secretion rates and mean residence times, VLDL subclass distribution, FFA concentration and rate of appearance in plasma, whole body substrate oxidation, and LPL and HL concentrations in plasma were not different during the FP and the LP. We conclude that VLDL-TG and VLDL-apoB-100 metabolism is not affected by menstrual cycle phase. sex hormones; stable isotope; lipid DYSLIPIDEMIA, characterized by increased plasma triglyceride (TG), increased total and LDL-cholesterol, and reduced HDLcholesterol concentrations, is a major risk factor for cardiovascular disease (41). Premenopausal women have a lesser risk of developing cardiovascular disease than age-matched men, but the "female advantage" disappears after menopause (26). Differences in plasma lipid concentrations, particularly plasma TG concentration, between men and women and pre-and postmenopausal women are likely responsible for this phenomenon. The increase in cardiovascular disease risk resulting from a given rise in plasma TG concentration is more than twofold higher for women than for men (23). Premenopausal women have lower plasma TG concentration than men (55); this difference between the sexes is abolished after menopause because of an increase in plasma TG concentration that coincides with the onset of menopause (10). This suggests a beneficial effect of ovarian hormones on plasma TG metabolism. Findings from studies in postmenopausal women receiving hormone replacement therapy and premenopausal women taking hormonal contraceptives indicate that this is likely due to the lack of progesterone rather than estradiol.Hormone replacement therapy providing progestins alone to postmenopausal women decreases fasting plasma TG concentration, whereas estrogens increase fasting plasma TG concentration (19). Also, estroge...