Vurallı Doğuş, Gönç E Nazlı, Özön Z Alev, Alikaşifoğlu Ayfer
Division of Pediatric Endocrinology, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Turk Pediatri Ars. 2020 Jun 19;55(2):131-138. doi: 10.14744/TurkPediatriArs.2019.03708. eCollection 2020.
To determine the clinical, anthropometric, and laboratory parameters that could be used for differentiating central precocious puberty from premature thelarche in girls who had breast development between the ages of 3 and 8 years.
The study included 344 girls (196 girls with idiopathic central precocious puberty, 148 girls with premature thelarche) who underwent gonadotropin- releasing hormone stimulation tests for breast development. Age at diagnosis, bone age, anthropometric measurements, basal/stimulated hormone levels were recorded. Univariate regression analysis was performed to determine the parameters that could be used for differentiating precocious puberty from premature thelarche. Significant parameters in univariate analyses were grouped according to the thresholds determined using receiver operating characteristic curves and reevaluated through multivariate analysis.
The bone age, height-standard deviation score, body mass index-standard deviation score, and growth velocity-standard deviation score at diagnosis were found to be higher; pubertal stages were found to be more advanced; uterus and ovary volumes were found to be larger; and the basal/peak luteinizing hormone, follicle-stimulating hormone, luteinizing hormone/follicle-stimulating hormone levels were found to be higher in the subjects with precocious puberty. There was no difference between estradiol levels between the two groups. The best thresholds to differentiate the two groups were found as 0.65 IU/L (78% sensitivity, 100% specificity), 1.9 IU/L (100% sensitivity, 72% specificity), 0.25 (67% sensitivity, 100% specificity) and 1.1 (69% sensitivity, 71% specificity), respectively, for basal luteinizing hormone, follicle-stimulating hormone, luteinizing hormone/follicle-stimulating hormone ratio, and the growth velocity-standard deviation score.
In girls presenting with early breast development, a basal luteinizing hormone level of ≥0.65 IU/L and a luteinizing hormone/follicle-stimulating hormone ratio of ≥0.25 are sensitive ways to demonstrate activation of the hypothalamo-pituitary-gonadal axis. Among these, the variable that gives the best sensitivity and specificity is the measurement of basal luteinizing hormone levels (≥0.65 IU/L), which can be used as a screening test in the diagnosis of central precocious puberty.
确定可用于区分3至8岁乳房发育女童中枢性性早熟与单纯性乳房早发育的临床、人体测量学和实验室参数。
该研究纳入了344名因乳房发育接受促性腺激素释放激素刺激试验的女童(196名特发性中枢性性早熟女童,148名单纯性乳房早发育女童)。记录诊断时的年龄、骨龄、人体测量数据、基础/刺激后激素水平。进行单因素回归分析以确定可用于区分性早熟与单纯性乳房早发育的参数。单因素分析中的显著参数根据使用受试者工作特征曲线确定的阈值进行分组,并通过多因素分析重新评估。
发现性早熟女童诊断时的骨龄、身高标准差评分、体重指数标准差评分和生长速度标准差评分更高;青春期阶段更 advanced;子宫和卵巢体积更大;基础/峰值促黄体生成素、促卵泡生成素、促黄体生成素/促卵泡生成素水平更高。两组之间雌二醇水平无差异。区分两组的最佳阈值分别为基础促黄体生成素0.65 IU/L(灵敏度78%,特异度100%)、促卵泡生成素1.9 IU/L(灵敏度100%,特异度72%)、促黄体生成素/促卵泡生成素比值0.25(灵敏度67%,特异度100%)和生长速度标准差评分1.1(灵敏度69%,特异度71%)。
在出现乳房早发育的女童中,基础促黄体生成素水平≥0.65 IU/L和促黄体生成素/促卵泡生成素比值≥0.25是证明下丘脑-垂体-性腺轴激活的敏感方法。其中,灵敏度和特异度最佳的变量是基础促黄体生成素水平测量(≥0.65 IU/L),可作为中枢性性早熟诊断的筛查试验。