Chan Crystal, Liu Kimberly
Centre for Fertility and Reproductive Health, Mount Sinai Hospital, 7th floor, 250 Dundas Street West, Toronto, ON, M5T 2Z5, Canada,
J Assist Reprod Genet. 2014 Oct;31(10):1317-21. doi: 10.1007/s10815-014-0312-2. Epub 2014 Aug 12.
Serum anti-mullerian hormone (AMH) has been proposed as a useful marker of ovarian reserve that is cycle-independent and predictive of outcome in assisted reproduction cycles. However, there is evidence that AMH production is gonadotropin-dependent, and that under the influence of FSH, growing follicles contribute to circulating AMH levels. Therefore, AMH testing may not be universally reflective of the primordial follicle pool in certain conditions. We demonstrate that in patients with idiopathic hypogonadotropic hypogonadism (IHH) and deficient gonadotropin production, AMH and antral follicle count (AFC) may not be reliable markers of ovarian reserve.
Case report.
Fertility clinic at a tertiary academic hospital.
A 30-year-old nulligravid patient with IHH who presented for fertility treatment with low FSH (0.3 IU/L), LH (0.1 IU/L), estradiol (77 pmol/L) and AMH levels (0.65 pmol/L), and an unmeasurable AFC.
A three-month course of priming with oral micronized 17β-estradiol, followed by daily injections of human menopausal gonadotropins (hMG).
AMH level and follicular development.
After 60 days of stimulation with hMG, the patient's AMH level increased to a peak of 1.27 pmol/L. After 102 days of stimulation, her estradiol level rose to 480 pmol/L and a 19 mm dominant follicle was detected. The patient successfully conceived with intrauterine insemination.
Ovarian reserve testing in patients with IHH can be challenging due to the contracted appearance of the ovaries and deficient FSH production. In these patients, AMH levels may underestimate ovarian reserve due to the lack of FSH-dependent growing follicles. When treated with a long course of hMG, these patients may exhibit increased AMH levels and demonstrate adequate follicular development.
血清抗苗勒管激素(AMH)已被认为是一种有用的卵巢储备标志物,它不受月经周期影响,可预测辅助生殖周期的结局。然而,有证据表明AMH的产生依赖促性腺激素,并且在促卵泡生成素(FSH)的影响下,生长中的卵泡会影响循环中的AMH水平。因此,在某些情况下,AMH检测可能无法普遍反映原始卵泡池的情况。我们证明,对于特发性低促性腺激素性性腺功能减退(IHH)且促性腺激素分泌不足的患者,AMH和窦卵泡计数(AFC)可能不是可靠的卵巢储备标志物。
病例报告。
一家三级学术医院的生殖诊所。
一名30岁未孕的IHH患者,前来接受生育治疗,其促卵泡生成素(FSH)水平低(0.3 IU/L)、促黄体生成素(LH)水平低(0.1 IU/L)、雌二醇水平低(77 pmol/L)、AMH水平低(0.65 pmol/L),且无法检测到AFC。
口服微粉化17β-雌二醇进行为期三个月的启动治疗,随后每日注射人绝经期促性腺激素(hMG)。
AMH水平和卵泡发育情况。
用hMG刺激60天后,患者的AMH水平升至峰值1.27 pmol/L。刺激102天后,其雌二醇水平升至480 pmol/L,并检测到一个19 mm的优势卵泡。该患者通过宫内人工授精成功受孕。
由于卵巢外观缩小和FSH分泌不足,对IHH患者进行卵巢储备检测可能具有挑战性。在这些患者中,由于缺乏FSH依赖的生长卵泡,AMH水平可能会低估卵巢储备。当接受长时间的hMG治疗时,这些患者可能会出现AMH水平升高,并表现出足够的卵泡发育。