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      Ovarian Lipid Metabolism Modulates Circulating Lipids in Premenopausal Women

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      The Journal of Clinical Endocrinology & Metabolism
      The Endocrine Society

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          Abstract

          <div class="section"> <a class="named-anchor" id="s1"> <!-- named anchor --> </a> <h5 class="section-title" id="d6905037e175">Context:</h5> <p id="d6905037e177">The premenopausal circulating lipid profile may be linked to the hormonal profile and ovarian lipid metabolism. </p> </div><div class="section"> <a class="named-anchor" id="s2"> <!-- named anchor --> </a> <h5 class="section-title" id="d6905037e180">Objective:</h5> <p id="d6905037e182">Assess how estradiol, progesterone, and ovarian lipid metabolism contributes to the premenopausal lipid profile; and evaluate the acute effects of a common hormonal oral contraceptive (OC) on circulating lipids. </p> </div><div class="section"> <a class="named-anchor" id="s3"> <!-- named anchor --> </a> <h5 class="section-title" id="d6905037e185">Design:</h5> <p id="d6905037e187">Experimental crossover with repeated measures.</p> </div><div class="section"> <a class="named-anchor" id="s4"> <!-- named anchor --> </a> <h5 class="section-title" id="d6905037e190">Setting:</h5> <p id="d6905037e192">Academic hospitals.</p> </div><div class="section"> <a class="named-anchor" id="s5"> <!-- named anchor --> </a> <h5 class="section-title" id="d6905037e195">Patients:</h5> <p id="d6905037e197">Eight healthy, regularly menstruating women.</p> </div><div class="section"> <a class="named-anchor" id="s6"> <!-- named anchor --> </a> <h5 class="section-title" id="d6905037e200">Interventions:</h5> <p id="d6905037e202">Participants underwent periodic serum sampling during a normal menstrual cycle; a standard 21-day, monophasic combined hormonal OC cycle (30 µg of ethinyl estradiol and 150 µg of levonorgestrel per day); menopause simulated by leuprolide acetate (22.5-mg depot); and an artificial menstrual cycle achieved via transdermal estradiol (50 to 300 µg/d) and vaginal micronized progesterone (100 to 300 mg/d). </p> </div><div class="section"> <a class="named-anchor" id="s7"> <!-- named anchor --> </a> <h5 class="section-title" id="d6905037e205">Main Outcome Measures:</h5> <p id="d6905037e207">Primary outcomes included evaluation of total cholesterol, high-density lipoprotein (HDL) cholesterol, low-density lipoprotein cholesterol, triglycerides, and the total cholesterol to HDL cholesterol ratio. To estimate the effect of estradiol, progesterone, and ovarian lipid metabolism, all specimens except those from the OC cycle were analyzed. Subgroup analysis was conducted on the follicular and luteal phases. In a separate analysis, the effect of the OC was evaluated relative to the normal menstrual cycle. </p> </div><div class="section"> <a class="named-anchor" id="s8"> <!-- named anchor --> </a> <h5 class="section-title" id="d6905037e210">Results:</h5> <p id="d6905037e212">Estradiol was significantly associated with increased levels of HDL cholesterol throughout the menstrual cycle and in the follicular phase. Ovarian effects were associated with reduced lipid levels, especially during the luteal phase. The OC was associated with an increased total cholesterol to HDL cholesterol ratio and triglycerides. </p> </div><div class="section"> <a class="named-anchor" id="s9"> <!-- named anchor --> </a> <h5 class="section-title" id="d6905037e215">Conclusion:</h5> <p id="d6905037e217">Previously unappreciated factors including ovarian lipid metabolism may contribute to the premenopausal lipid profile. </p> </div><p class="first" id="d6905037e220">We studied how estradiol, progesterone, and ovarian effects mediate circulating lipids in premenopausal women and found a novel role for the corpus luteum in reducing low-density lipoprotein cholesterol. </p>

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          Most cited references17

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          Sex differences in lipid and lipoprotein metabolism: it's not just about sex hormones.

          It is commonly thought that sex hormones are important regulators of plasma lipid kinetics and are responsible for sexual dimorphism in the plasma lipid profile. Here we discuss the findings from studies evaluating lipid and lipoprotein kinetics in men and women in the context of what we know about the effects of exogenous sex hormone administration, and we conclude that it is more complicated than that. It has become clear that normal physiological alterations in the hormonal milieu (i.e. due to menopause or throughout the menstrual cycle) do not significantly affect plasma lipid homeostasis. Furthermore, parenterally administered estrogens have either no effect or only very small beneficial effects, whereas orally administered estrogens raise plasma triglyceride concentrations--a phenomenon that is not consistent with the observed sex differences and likely results from the hepatic "first-pass effect." The effects of progestogens and androgens mimic only in part the differences in plasma lipids between men and women. Thus, the underlying physiological modulators of plasma lipid metabolism responsible for the differences between men and women remain to be elucidated.
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            Effects of Estrogen or Estrogen/ Progestin Regimens on Heart Disease Risk Factors in Postmenopausal Women

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              • Record: found
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              • Article: not found

              Effects of postmenopausal estrogen replacement on the concentrations and metabolism of plasma lipoproteins.

              Postmenopausal estrogen-replacement therapy may reduce the risk of cardiovascular disease, and this beneficial effect may be mediated in part by favorable changes in plasma lipid levels. However, the effects on plasma lipoprotein levels of postmenopausal estrogens in the low doses currently used have not been precisely quantified, and the mechanism of these effects is unknown. We conducted two randomized, double-blind crossover studies in healthy postmenopausal women who had normal lipid values at base line. In study 1, 31 women received placebo and conjugated estrogens at two doses (0.625 mg and 1.25 mg per day), each treatment for three months. In study 2, nine women received placebo, oral micronized estradiol (2 mg per day), and transdermal estradiol (0.1 mg twice a week), each treatment for six weeks. The metabolism of very-low-density lipoprotein (VLDL) and low-density lipoprotein (LDL) was measured by endogenously labeling their protein component, apolipoprotein B. In study 1, the conjugated estrogens at doses of 0.625 mg per day and 1.25 mg per day decreased the mean LDL cholesterol level by 15 percent (95 percent confidence interval, 11 to 19 percent; P less than 0.0001) and 19 percent (95 percent confidence interval, 15 to 23 percent; P less than 0.0001), respectively; increased the HDL cholesterol level by 16 percent (95 percent confidence interval, 12 to 20 percent; P less than 0.0001) and 18 percent (95 percent confidence interval, 14 to 22 percent; P less than 0.0001), respectively; and increased VLDL triglyceride levels by 24 percent (95 percent confidence interval, 8 to 40 percent; P less than 0.003) and 42 percent (95 percent confidence interval, 26 to 58 percent; P less than 0.0001), respectively. In study 2, oral estradiol increased the mean concentration of large VLDL apolipoprotein B by 30 +/- 10 percent (P = 0.05) by increasing its production rate by 82 +/- 18 percent (P less than 0.01). Most of this additional large VLDL was cleared directly from the circulation and was not converted to small VLDL or LDL. Oral estradiol reduced LDL cholesterol concentrations by 14 +/- 3 percent (P less than 0.005), because LDL catabolism increased by 36 +/- 7 percent (P less than 0.005). The oral estradiol increased the HDL cholesterol level by 15 +/- 2 percent (P less than 0.0001). Transdermal estradiol had no effect. The postmenopausal use of oral estrogens in low doses favorably alters LDL and HDL levels that may protect women against atherosclerosis, while minimizing potentially adverse effects on triglyceride levels. The decrease in LDL levels results from accelerated LDL catabolism; the increase in triglyceride levels results from increased production of large, triglyceride-rich VLDL.
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                Author and article information

                Journal
                The Journal of Clinical Endocrinology & Metabolism
                The Endocrine Society
                0021-972X
                1945-7197
                September 01 2017
                September 01 2017
                January 06 2017
                September 01 2017
                September 01 2017
                January 06 2017
                : 102
                : 9
                : 3138-3145
                Article
                10.1210/jc.2016-3456
                5587059
                28323981
                570f52f5-ea60-4bfb-80e9-89802e5a13e4
                © 2017
                History

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