Gaspard U, Endrikat J, Desager J P, Buicu C, Gerlinger C, Heithecker R
Department of Gynecology, University of Liege, Sart Tilman University Hospital, Liège, Belgium.
Contraception. 2004 Apr;69(4):271-8. doi: 10.1016/j.contraception.2003.11.003.
In this open-label, randomized study we compared the influence of a new oral contraceptive containing 30 microg ethinylestradiol and 3 mg drospirenone (EE + DRSP = Yasmin), with a reference preparation containing 30 microg ethinylestradiol and 150 microg desogestrel (EE + DSG = Marvelon) on the lipid profile. The primary target variables were total high-density lipoprotein (HDL) cholesterol, HDL2 cholesterol and low-density lipoprotein (LDL) cholesterol. These and additional lipid and lipoprotein fractions were measured at baseline and in the 3rd, 6th and 13th treatment cycles in a total of 50 volunteers, and also assessed after density gradient ultracentrifugation. A slight increase in mean total HDL cholesterol vs. baseline was found for the DRSP group (+12.8%) and the DSG group (+11.8%) after 13 treatment cycles. HDL2 cholesterol did not change remarkably in both groups. The mean LDL cholesterol values increased by 10.6% vs. baseline in the DSG group and remained nearly stable in the DRSP group (+1.8%). All measured values remained within the reference ranges. No statistically significant differences were found between the two treatment groups for those primary endpoints. A slight rise in mean total cholesterol was found for all cycles after the initiation of treatment. The mean increase after 1 year of treatment was approximately 8% in both treatment groups. Mean triglyceride levels increased for both treatment groups without leaving the reference range. The increase for total triglycerides was +73.6 % in the DRSP group and +61.3% in DSG group. For total phospholipids, an increase of +13.6% (DRSP) and +18.5% (DSG) over 13 cycles was measured. The apolipoproteins Apo A-I, Apo A-II and Apo B increased slightly more during DRSP treatment than during DSG treatment. The reduction of Apo E was similar in both groups. Lipoprotein (a) remained stable in the DRSP group, whereas it increased by +10.8% in the DSG group. In conclusion, the combined low-dose oral contraceptive Yasmin, with 30 microg ethinylestradiol and 3 mg of the novel progestogen drospirenone, as well as the reference preparation, had little impact on the lipid profile. While both preparations displayed a favorable lipid profile with increased total HDL cholesterol, the antiandrogenic or missing androgenic activity of Yasmin may be regarded as responsible for the stable LDL cholesterol levels. As a result, the ratio of total HDL:LDL was increased, a pattern that is usually considered clinically beneficial with respect to cardiovascular disease risk.
在这项开放标签的随机研究中,我们比较了一种含30微克炔雌醇和3毫克屈螺酮的新型口服避孕药(炔雌醇 + 屈螺酮 = 优思明)与一种含30微克炔雌醇和150微克去氧孕烯的对照制剂(炔雌醇 + 去氧孕烯 = 妈富隆)对血脂谱的影响。主要目标变量为总高密度脂蛋白(HDL)胆固醇、HDL2胆固醇和低密度脂蛋白(LDL)胆固醇。在总共50名志愿者的基线期以及第3、6和13个治疗周期测量了这些以及其他脂质和脂蛋白组分,并在密度梯度超速离心后进行了评估。在13个治疗周期后,屈螺酮组(+12.8%)和去氧孕烯组(+11.8%)的平均总HDL胆固醇相较于基线有轻微升高。两组的HDL2胆固醇均无明显变化。去氧孕烯组的平均LDL胆固醇值相较于基线升高了10.6%,而屈螺酮组几乎保持稳定(+1.8%)。所有测量值均保持在参考范围内。两个治疗组在这些主要终点方面未发现统计学上的显著差异。治疗开始后的所有周期中,平均总胆固醇均有轻微升高。两个治疗组在治疗1年后的平均升高幅度约为8%。两个治疗组的平均甘油三酯水平均升高,但未超出参考范围。屈螺酮组总甘油三酯的升高幅度为 +73.6%,去氧孕烯组为 +61.3%。在13个周期中,总磷脂的升高幅度为屈螺酮组 +13.6%,去氧孕烯组 +18.5%。载脂蛋白Apo A-I、Apo A-II和Apo B在屈螺酮治疗期间的升高幅度略大于去氧孕烯治疗期间。两组中Apo E的降低情况相似。脂蛋白(a)在屈螺酮组保持稳定,而在去氧孕烯组升高了 +10.8%。总之,含30微克炔雌醇和3毫克新型孕激素屈螺酮的复方低剂量口服避孕药优思明以及对照制剂对血脂谱影响较小。虽然两种制剂均显示出总HDL胆固醇升高的有利血脂谱,但优思明的抗雄激素活性或缺乏雄激素活性可能是LDL胆固醇水平稳定的原因。因此,总HDL:LDL的比值升高,这种模式通常被认为对心血管疾病风险在临床上有益。