Wu Vickie, Zhao Victoria, Issa Rula, Wilkes Meredith, Wallach Elizabeth, Rapaport Robert, Romero Christopher, Yau Mabel
Department of Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Department of Pediatric Endocrinology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Ann Pediatr Endocrinol Metab. 2021 Sep;26(3):185-191. doi: 10.6065/apem.2040220.110. Epub 2021 May 12.
This study aimed to evaluate the time interval to menarche after gonadotropin-releasing hormone agonist (GnRHa) treatment in females with central precocious puberty (CPP) and to identify factors contributing to timing of menarche.
We retrospectively reviewed medical records of 39 females with CPP who reached menarche after GnRHa treatment (leuprolide or histrelin). CPP diagnostic criteria were breast development at <8 years old, measurable pubertal luteinizing hormone and/or estradiol concentrations, and bone age advancement. Indications to treat were advanced bone age and psychosocial concerns. Descriptive summaries were reported as frequency and proportion for categorical variables and mean and standard deviation for continuous measures. Linear regression models were developed to evaluate the associations of clinical factors with the time interval to menarche.
Mean age was 9.4±1.6 years at treatment onset, and treatment duration was 2.2±1.4 years. Menarche occurred at 12.6±1.1 years, which was 1.04±0.5 years after treatment discontinuation. This was negatively associated with Tanner stage of breast development and bone age at treatment onset and change in bone age during treatment. No association was seen between time interval to menarche and treatment duration, medication, or body mass index.
We found the average time interval to menarche after GnRHa treatment in our population of female patients with CPP to be 1.04±0.5 years; this is in agreement with other reports. Tanner stage of breast development, bone age at treatment onset, and change in bone age were negatively associated with time interval to menarche. These data provide clinical correlates that assist providers during anticipatory guidance of patients with CPP after GnRHa treatment.
本研究旨在评估中枢性性早熟(CPP)女性患者接受促性腺激素释放激素激动剂(GnRHa)治疗后月经初潮的时间间隔,并确定影响月经初潮时间的因素。
我们回顾性分析了39例接受GnRHa(亮丙瑞林或戈舍瑞林)治疗后月经初潮的CPP女性患者的病历。CPP的诊断标准为8岁前乳房发育、可测量的青春期促黄体生成素和/或雌二醇浓度以及骨龄提前。治疗指征为骨龄提前和心理社会问题。分类变量的描述性总结以频率和比例报告,连续测量指标以均值和标准差报告。建立线性回归模型以评估临床因素与月经初潮时间间隔的关联。
治疗开始时的平均年龄为9.4±1.6岁,治疗持续时间为2.2±1.4年。月经初潮发生在12.6±1.1岁,即在停药后1.04±0.5年。这与治疗开始时乳房发育的 Tanner 分期和骨龄以及治疗期间骨龄的变化呈负相关。月经初潮时间间隔与治疗持续时间、药物或体重指数之间未发现关联。
我们发现,在我们的CPP女性患者群体中,GnRHa治疗后月经初潮的平均时间间隔为1.04±0.5年;这与其他报告一致。乳房发育的 Tanner 分期、治疗开始时的骨龄以及骨龄变化与月经初潮时间间隔呈负相关。这些数据提供了临床关联,有助于医生在对接受GnRHa治疗的CPP患者进行预期指导时提供参考。