Department of Obstetrics, Gynecology and Reproductive Sciences, College of Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Department of Community Health and Epidemiology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Menopause. 2018 Apr;25(4):399-407. doi: 10.1097/GME.0000000000001021.
The aim of the study was to test the hypothesis that the development of luteal phase dominant follicles (LPDFs) as women age is associated with abnormal luteal function.
Luteal and antral follicle diameter were quantified in ovulatory women of midreproductive age (MRA; 18-35 y; n = 9) and advanced reproductive age (ARA; 45-55 y; n = 16) every 1 to 3 days during one complete interovulatory interval. Blood was drawn at each visit and assayed for progesterone, estradiol, inhibin A, follicle-stimulating hormone, and luteinizing hormone. Luteal diameter and hormone profiles were compared within MRA and ARA women with versus without LPDFs.
Luteal growth and regression profiles were similar in MRA women with typical versus no LPDFs (13.9, 14.8 mm; P > 0.1); however, luteal phase estradiol and progesterone were greater in MRA women with typical (91.1 ng/L, 8.81 μg/L) versus no (48.8 ng/L, 7.32 μg/L) LPDFs, respectively (LPDF effect, P < 0.1). In the ARA group, mean luteal diameter was lowest in women with atypical LPDFs (12.3 mm), greatest in those with typical LPDFs (16.0 mm), and moderate in those with no LPDFs (13.6 mm), (P < 0.1). Reduced luteal growth in ARA women with atypical versus typical and/or no LPDFs occurred simultaneously to greater luteal phase estradiol (199 vs 69.0, 78.4 ng/L) lower progesterone (7.38 vs 10.7, 13.8 ug/L), and lower inhibin A (36.3, 35.6, 51.2) (P < 0.1).
The development of LPDFs as women age was associated with reduced luteal growth, greater estradiol, lower progesterone, and lower inhibin A. These findings provide preliminary evidence that variations in antral folliculogenesis contribute to luteal insufficiency during the menopausal transition.
本研究旨在验证这样一个假设,即随着女性年龄的增长,黄体期主导卵泡(LPDFs)的发育与黄体功能异常有关。
在一个完整的排卵间期内,每隔 1 至 3 天,对处于生育中期(18-35 岁;n=9)和生育晚期(45-55 岁;n=16)的排卵女性的黄体和窦卵泡直径进行量化。每次就诊时都抽取血液并检测孕激素、雌二醇、抑制素 A、卵泡刺激素和黄体生成素。比较生育中期和晚期有和无 LPDFs 的女性的黄体直径和激素谱。
生育中期有典型和无典型 LPDFs 的女性黄体生长和退化曲线相似(13.9、14.8mm;P>0.1);然而,生育中期有典型(91.1ng/L,8.81μg/L)和无 LPDFs(48.8ng/L,7.32μg/L)的女性黄体中期雌二醇和孕激素水平更高(LPDF 效应,P<0.1)。在生育晚期组中,无典型 LPDFs 的女性平均黄体直径最低(12.3mm),有典型 LPDFs 的女性最大(16.0mm),无 LPDFs 的女性居中(13.6mm)(P<0.1)。与典型和/或无 LPDFs 的女性相比,生育晚期有非典型 LPDFs 的女性黄体生长减少,黄体中期雌二醇水平升高(199 比 69.0、78.4ng/L),孕激素水平降低(7.38 比 10.7、13.8μg/L),抑制素 A 水平降低(36.3、35.6、51.2)(P<0.1)。
随着女性年龄的增长,LPDFs 的发育与黄体生长减少、雌二醇升高、孕激素降低和抑制素 A 降低有关。这些发现初步表明,窦卵泡发生的变化可能导致绝经过渡期间黄体功能不足。