Godsland I F, Crook D, Wynn V
Wynn Institute for Metabolic Research, London, United Kingdom.
Am J Obstet Gynecol. 1992 Jun;166(6 Pt 2):1955-63. doi: 10.1016/0002-9378(92)91395-q.
Newer lower dose formulations are associated with an improved cardiovascular disease risk marker profile, which supports their use for longer periods and among older women. Epidemiologic studies of the newer formulations are limited. Without clinical information, an evaluation of the effects of more recent formulations on metabolic risk markers for cardiovascular disease is useful. In a large cross-sectional study, a reduction in the progestin dose and use of alternative progestins substantially reduced the proportion of oral contraceptive users with values associated with an increased risk of cardiovascular disease. No progression in metabolic changes was found by analyzing the effect of the duration of oral contraceptive use. The user's age interacted positively with the oral contraceptive--induced increase in serum triglyceride levels, but there was no interaction of age with the oral contraceptive's effect on oral glucose tolerance, glucose and insulin responses, low-density lipoprotein cholesterol, or high-density lipoprotein subfraction 2 cholesterol levels.
新型低剂量制剂与改善的心血管疾病风险标志物谱相关,这支持它们在更长时期以及老年女性中使用。关于新型制剂的流行病学研究有限。在缺乏临床信息的情况下,评估最新制剂对心血管疾病代谢风险标志物的影响是有用的。在一项大型横断面研究中,孕激素剂量的降低和替代孕激素的使用大幅降低了口服避孕药使用者中与心血管疾病风险增加相关指标值的比例。通过分析口服避孕药使用时长的影响,未发现代谢变化的进展。使用者年龄与口服避孕药引起的血清甘油三酯水平升高呈正相关,但年龄与口服避孕药对口服葡萄糖耐量、血糖和胰岛素反应、低密度脂蛋白胆固醇或高密度脂蛋白亚组分2胆固醇水平的影响之间没有相互作用。