Legro Richard S, Kunselman Allen R, Stetter Christy M, Gnatuk Carol L, Estes Stephanie J, Brindle Eleanor, Vesper Hubert W, Botelho Julianne C, Lee Peter A, Dodson William C
Departments of Obstetrics and Gynecology.
Public Health Sciences, and.
J Clin Endocrinol Metab. 2017 Jan 1;102(1):122-131. doi: 10.1210/jc.2016-2707.
Daughters of women with polycystic ovary syndrome (PCOS) are thought to be at increased risk for developing stigmata of the syndrome, but the ontogeny during puberty is uncertain.
We phenotyped daughters (n = 76) of mothers with PCOS and daughters (n = 80) from control mothers for reproductive and metabolic parameters characteristic of PCOS.
DESIGN, SETTING, AND PARTICIPANTS: We performed a matched case/control study at Penn State Hershey Medical Center that included non-Hispanic, white girls 4 to 17 years old.
We obtained birth history, biometric, ovarian ultrasounds, whole-body dual-energy X-ray absorptiometry scan for body composition, 2-hour glucose challenged salivary insulin levels, and two timed urinary collections (12 hours overnight and 3 hours in the morning) for gonadotropins and sex steroids.
We measured integrated urinary levels of adrenal (dehydroepiandrosterone sulfate) and ovarian [testosterone (TT)] steroids. Other endpoints included integrated salivary insulin levels and urinary luteinizing hormone levels.
There were no differences in detection rates or mean levels for gonadotropins and sex steroids in timed urinary collections between PCOS daughters and control daughters, nor were there differences in integrated salivary insulin levels. Results showed that 69% of Tanner 4/5 PCOS daughters vs 31% of control daughters had hirsutism defined as a Ferriman-Gallwey score >8 (P = 0.04). There were no differences in body composition as determined by dual-energy X-ray absorptiometry between groups in the three major body contents (i.e., bone, lean body mass, and fat) or in ovarian volume between groups.
Matched for pubertal stage, PCOS daughters have similar levels of urinary androgens and gonadotropins as well as glucose-challenged salivary insulin levels.
多囊卵巢综合征(PCOS)女性的女儿被认为患该综合征特征性体征的风险增加,但青春期的个体发育情况尚不确定。
我们对患有PCOS母亲的女儿(n = 76)和对照母亲的女儿(n = 80)进行了PCOS特征性生殖和代谢参数的表型分析。
设计、地点和参与者:我们在宾夕法尼亚州立大学赫尔希医学中心进行了一项匹配病例/对照研究,纳入了4至17岁的非西班牙裔白人女孩。
我们获取了出生史、人体测量数据、卵巢超声检查、用于身体成分分析的全身双能X线吸收法扫描、2小时葡萄糖激发唾液胰岛素水平,以及两次定时尿液收集(夜间12小时和上午3小时)以检测促性腺激素和性类固醇。
我们测量了肾上腺(硫酸脱氢表雄酮)和卵巢[睾酮(TT)]类固醇的综合尿液水平。其他终点指标包括综合唾液胰岛素水平和尿液促黄体生成素水平。
PCOS女儿和对照女儿在定时尿液收集的促性腺激素和性类固醇检测率或平均水平上没有差异,综合唾液胰岛素水平也没有差异。结果显示,69%的坦纳4/5期PCOS女儿与31%的对照女儿有多毛症,定义为费里曼 - 盖尔韦评分>8(P = 0.04)。两组在三种主要身体成分(即骨骼、瘦体重和脂肪)的双能X线吸收法测定的身体成分或卵巢体积方面没有差异。
在青春期阶段匹配的情况下,PCOS女儿的尿液雄激素、促性腺激素水平以及葡萄糖激发唾液胰岛素水平相似。