Carr B R, Marshburn P B, Weatherall P T, Bradshaw K D, Breslau N A, Byrd W, Roark M, Steinkampf M P
Department of Obstetrics and Gynecology, University of Texas Southwestern Medical Center, Dallas 75235-9032.
J Clin Endocrinol Metab. 1993 May;76(5):1217-23. doi: 10.1210/jcem.76.5.8496313.
The purpose of this study was to prospectively compare the effectiveness of administering medroxyprogesterone acetate (MPA; 20 mg/day) in either the first (protocol A) or last (protocol B) 12-week period along with a 6-month course of the GnRH analog (GnRH-a; leuprolide acetate; 1 mg/day, sc) on uterine and leiomyomata volumes and hormone (estradiol, LH, and FSH) and serum lipid (total cholesterol, triglycerides, and high and low density lipoprotein) levels. Sixteen women were randomized into protocol A or B, received either MPA or placebo along with GnRH-a, respectively, and were then crossed over at 12 weeks to placebo or MPA, respectively, for the final 12-week interval of GnRH-a therapy. Total, myoma, and nonmyoma uterine volumes were determined by magnetic resonance imaging, and serum studies were performed at the beginning of the study and at 12 and 24 weeks. In both protocols, LH and estradiol levels declined by 80-90% (P < 0.03) and 55-72% (P < 0.02) of the baseline, respectively, at 12 weeks and remained at this level at 24 weeks. There were no significant changes in the other laboratory tests between protocols or longitudinally over time. Total uterine volume decreased to 73% of the baseline at 12 weeks in protocol B (P < 0.04), but did not change in protocol A. After crossover at 12 weeks, the total uterine volume of women in protocol A decreased to 74% of the baseline (P < 0.02) at 24 weeks. Between-protocol comparisons demonstrated a greater decline in total uterine volume in protocol B than A at 12 weeks, but after cross-over, MPA addition was associated with a significant increase in total uterine volume (protocol B) compared to a decrease in protocol A at 24 weeks (P < 0.005). In contrast, although myoma volume declined in both protocols, no significant changes in myoma volume were detected within or between groups over the treatment period. Nonmyoma volume changes in protocols A and B roughly paralleled total uterine volume changes, with MPA coadministration showing a correlation with a reversal in the GnRH-a-associated decrease in nonmyomatous tissue volume.(ABSTRACT TRUNCATED AT 400 WORDS)
本研究的目的是前瞻性地比较在GnRH类似物(GnRH-a;醋酸亮丙瑞林;1毫克/天,皮下注射)6个月疗程的第一个12周期间(方案A)或最后12周期间(方案B)给予醋酸甲羟孕酮(MPA;20毫克/天)对子宫及子宫肌瘤体积以及激素(雌二醇、促黄体生成素和促卵泡生成素)和血脂(总胆固醇、甘油三酯以及高密度和低密度脂蛋白)水平的影响。16名女性被随机分为方案A或方案B,分别接受MPA或安慰剂联合GnRH-a治疗,然后在12周时交叉分别接受安慰剂或MPA,用于GnRH-a治疗的最后12周间隔。通过磁共振成像测定子宫总体积、肌瘤体积和非肌瘤子宫体积,并在研究开始时、12周和24周进行血清学检查。在两个方案中,促黄体生成素和雌二醇水平在12周时分别下降至基线水平的80 - 90%(P < 0.03)和55 - 72%(P < 0.02),并在24周时维持在该水平。方案之间或随时间纵向观察,其他实验室检查均无显著变化。方案B中子宫总体积在12周时降至基线的73%(P < 0.04),但方案A中未发生变化。在12周交叉后,方案A中女性的子宫总体积在24周时降至基线的74%(P < 0.02)。方案间比较显示,方案B在12周时子宫总体积的下降幅度大于方案A,但交叉后,与方案A在24周时子宫总体积下降相比,方案B中添加MPA与子宫总体积显著增加相关(P < 0.005)。相比之下,虽然两个方案中肌瘤体积均下降,但在治疗期间组内或组间均未检测到肌瘤体积的显著变化。方案A和方案B中非肌瘤体积变化大致与子宫总体积变化平行,联合使用MPA显示与GnRH-a相关的非肌瘤组织体积减少的逆转存在相关性。(摘要截选至400字)