Use of oral estradiol plus vaginal progesterone in healthy postmenopausal women

被引:6
作者
Sriprasert, Intira [1 ]
Mert, Melissa [2 ]
Mack, Wendy J. [2 ,3 ]
Hodis, Howard N. [2 ,3 ,4 ]
Shoupe, Donna [1 ,2 ]
机构
[1] Univ Southern Calif, Keck Sch Med, Dept Obstet & Gynecol, 2020 Zonal Ave,IRD 218, Los Angeles, CA 90033 USA
[2] Univ Southern Calif, Keck Sch Med, Dept Populat & Publ Hlth Sci, Los Angeles, CA 90007 USA
[3] Univ Southern Calif, Keck Sch Med, Atherosclerosis Res Unit, Los Angeles, CA 90007 USA
[4] Univ Southern Calif, Keck Sch Med, Dept Med, Los Angeles, CA 90007 USA
基金
美国国家卫生研究院;
关键词
Vaginal progesterone; Estradiol; Postmenopause; Endometrium; Cervical cytology; HORMONE REPLACEMENT THERAPY; CORONARY-HEART-DISEASE; GLOBAL CONSENSUS STATEMENT; PRIMARY PREVENTION; REPRODUCTIVE LIFE; TIMING HYPOTHESIS; PARADIGM SHIFT; ARTERIES VARY; ATHEROSCLEROSIS; ESTROGEN;
D O I
10.1016/j.maturitas.2021.09.002
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Objectives: To compare the effect of oral estradiol (E2) plus vaginal progesterone (P4) against placebo on endometrial thickness, endometrial biopsy pathology, cervical cytology and total cancer incidence among healthy postmenopausal women. Study design: This study is a sub-analysis of the Early versus Late Intervention Trial with Estradiol (ELITE), a randomized, double-blinded, placebo-controlled trial that previously demonstrated that hormone therapy (HT) was associated with less progression of subclinical atherosclerosis than placebo when therapy was initiated within 6 years after menopause but not when it was initiated 10 or more years after menopause. This sub-analysis included only ELITE participants with an intact uterus, who were randomized to either daily oral micronized 17beta-E2 1 mg/day with 4% vaginal micronized P4 gel 45 mg/day for 10 days each month or placebo. Main outcome measures: Participants were evaluated at baseline and annually during a median follow-up of 4.8 years for endometrial thickness as determined by pelvic transvaginal ultrasound followed by an endometrial biopsy when indicated, and cervical cytology and cancer incidence. Results: Over up to 80 months of follow-up, participants randomized to oral E2 plus vaginal P4 had progressive and statistically significant increases in endometrial thickness (p<0.001), underwent more endometrial biopsies and had a higher rate of endometrial hyperplasia on endometrial biopsy compared with the placebo group. Due to the close follow-up of participants in the trial protocol, these abnormal findings were effectively treated. Conclusion: Our results suggest that 10 days of vaginal P4 45 mg/day is insufficient to completely oppose the effect of oral E2 1 mg/day on the endometrium. Further studies are needed to test alternative doses or frequencies of administration of vaginal P4 for adequate endometrial protection from E2 therapy among postmenopausal women. ClinicalTrials.gov registration NCT00114517
引用
收藏
页码:13 / 19
页数:7
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