在月经后过渡期有多囊卵巢综合征风险的女孩中不同生殖表型的个体发生。

IF 5.1
Laura C Torchen, Apoorva Aekka, Kelly Brewer, Ryan Sisk, Sarayu Ratnam, Camila Vendrami, Frank H Miller, Andrea Dunaif
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引用次数: 0

摘要

背景:多囊卵巢综合征(PCOS-d)女性和超重/肥胖(low -g)女孩的女儿在儿童期开始患有高雄激素血症(HA)。然而,他们早期生殖表型的其他特征不同,表明有不同的机制赋予多囊卵巢综合征的风险增加。目的:我们进行了一项横断面研究的青春期女孩在早期月经后的过渡。设计、环境和参与者:PCOS-d (n=15)、OW-g (n=12)和lean control女孩(LC, n=17)在月经初潮后0.2-1.2年内进行研究。评估代谢和生殖表型。结果:SHBG水平较低(P45 d)或结论:PCOS-d和low -g在月经后早期过渡期间均存在持续性HA。然而,仅在PCOS-d中观察到OD和神经内分泌异常,GnRH类似物的基础和刺激的LH反应升高。这些发现支持了导致PCOS的不同发育轨迹的存在,PCOS-d的早期神经内分泌失调和low -g的外周(可能与肥胖相关)雄激素过量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Ontogeny of Distinct Reproductive Phenotypes in Girls at Risk for PCOS During the Postmenarchal Transition.

Context: Daughters of women with PCOS (PCOS-d) and girls with overweight/obesity (OW-g) have hyperandrogenemia (HA) beginning in childhood. However, other features of their early reproductive phenotypes differ, suggesting that there are distinct mechanisms conferring increased risk for PCOS.

Objective: We performed a cross sectional study of adolescent girls during the early postmenarchal transition.

Design, setting, and participants: PCOS-d (n=15), OW-g (n=12) and lean control girls (LC, n=17), were studied within 0.2-1.2 yrs of menarche. Metabolic and reproductive phenotypes were assessed.

Results: SHBG levels were lower (P<0.0001) in PCOS-d and OW-g vs. LC. Free T levels were higher (P=0.02) in OW-g vs. LC. DHEAS levels were higher (P=0.04) in PCOS-d vs. LC, and trended higher in OW-g vs. LC (P=0.07). Morning LH levels were higher in PCOS-d vs. OW-g (P=0.02). LH and FSH responses to GnRH analog were also increased in PCOS-d vs. OW-g (LH AUC P=0.006, FSH AUC P=0.01). The prevalence of HA was similarly increased in PCOS-d and OW-g vs. LC (χ2 P=0.04). The prevalence of ovulatory dysfunction (OD, menses >45 d or <21 d) was increased (χ2 P=0.05) in PCOS-d vs. OW-g and LC.

Conclusions: Both PCOS-d and OW-g had persistent HA during the early postmenarchal transition. However, OD and neuroendocrine abnormalities, elevated basal and stimulated LH responses to GnRH analog, were observed only in PCOS-d. These findings support the existence of distinct developmental trajectories leading to PCOS, with early neuroendocrine dysregulation in PCOS-d and peripheral, likely adiposity-related, androgen excess in OW-g.

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