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Changes in body mass index during gonadotropin-releasing hormone agonist treatment for central precocious puberty and early puberty

机译:促性腺激素释放激素激动剂治疗中枢性早熟和青春期早期的体重指数变化

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Gonadotropin-releasing hormone agonists (GnRHa) have been widely used for decades to treat patients with central precocious puberty (CPP). Several studies have investigated changes in body composition in patients with CPP following GnRHa treatment, but the results are inconsistent. The aim of this study was to investigate changes in body mass index (BMI) in children treated with GnRHa for 2 years. We also assessed whether BMI affects treatment outcomes. This study included 383 girls (214 girls with central precocious puberty and 169 girls who underwent early puberty) treated with depot leuprolide acetate monthly for at least 2 years. We analyzed changes in BMI standard deviation score (SDS). Furthermore, blood luteinizing hormone (LH) levels were determined 30 min after depot leuprolide acetate administration every 6 months to evaluate adequate suppression of the hypothalamic-pituitary-gonadal axis. Pretreatment mean BMI SDS values were 0.07 +/- 0.69, 1.29 +/- 0.16, and 1.95 +/- 0.32 in the normal weight, overweight, and obese subjects, respectively. Mean BMI SDS values after 2 years of treatment increased significantly only in normal weight children (0.07 +/- 0.69 vs. 0.25 +/- 0.73, P < 0.001). LH levels 30 min after leuprolide injection after 2 years of treatment were not different among normal weight, overweight, and obese subjects. Although the difference in BMI SDS was relatively small, it standard deviation score increased significantly after 2 years of treatment in normal weight girls with early pubertal development.
机译:促性腺激素释放激素激动剂(GnRHa)已广泛用于治疗中枢性性早熟(CPP)的患者数十年。几项研究调查了GnRHa治疗后CPP患者身体成分的变化,但结果不一致。这项研究的目的是调查接受GnRHa治疗2年的儿童的体重指数(BMI)的变化。我们还评估了BMI是否会影响治疗效果。这项研究包括383名女孩(其中214名患有中枢性早熟的女孩,还有169名经历了青春期的年轻女孩),每月接受醋酸亮丙瑞林治疗至少2年。我们分析了BMI标准差评分(SDS)的变化。此外,每6个月注射醋酸亮丙瑞林30分钟后,测定血液黄体生成素(LH)水平,以评估下丘脑-垂体-性腺轴的充分抑制。正常体重,超重和肥胖受试者的治疗前平均BMI SDS值分别为0.07 +/- 0.69、1.29 +/- 0.16和1.95 +/- 0.32。治疗2年后的平均BMI SDS值仅在正常体重儿童中显着增加(0.07 +/- 0.69对0.25 +/- 0.73,P <0.001)。正常体重,超重和肥胖受试者在治疗2年后注射亮丙瑞林30分钟后LH水平无差异。尽管BMI SDS的差异相对较小,但在正常体重的青春期早期发育女孩中,治疗2年后其标准差评分显着增加。

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