Koehler B, Koehler M, Osuch-Jaczewska R
Pediatric Endocrinology Clinic, Silesian Academy of Medicine, Katowice, Poland.
Exp Clin Endocrinol. 1988 Mar;92(3):252-6. doi: 10.1055/s-0029-1210811.
The agonistic analogues of luteinizing hormone releasing hormone were used in the treatment of precocious puberty (pp) in children. 12 children with pp were treated for 6 months with an intranasal LH-RH analogue (C6-C3-C2-naphtyl/D-alanine)-LHRH. The majority of the children had central precocious puberty. Only one child had peripheral pp. Laboratory assessment of estradiol, testosterone, LH and FSH levels revealed that 1,000 micrograms/day of this analogue diminished the hormone levels only in the group of children with central and combined pp. Bone age, pelvic ultrasound examination, sexual development and growth rate were determined pre-, during and after the treatment. The growth velocity decreased and gonadal and sexual characteristic ceased advancing after the LH-RH therapy. Biochemical and hematological studies performed in our children did not show any significant changes during the treatment periods. No adverse effects were noted from the intranasal therapy. We conclude, that intranasal therapy is safe, convenient and effective in pp, but not of peripheral origin.
促黄体生成激素释放激素的激动剂类似物被用于治疗儿童性早熟(PP)。12名患有PP的儿童接受了鼻内促黄体生成激素释放激素类似物(C6-C3-C2-萘基/D-丙氨酸)-促黄体生成激素释放激素治疗6个月。大多数儿童患有中枢性性早熟。只有一名儿童患有外周性PP。对雌二醇、睾酮、促黄体生成素和促卵泡生成素水平的实验室评估显示,每天1000微克这种类似物仅能降低中枢性和混合型PP儿童组的激素水平。在治疗前、治疗期间和治疗后测定骨龄、盆腔超声检查、性发育和生长速度。促黄体生成激素释放激素治疗后,生长速度下降,性腺和性征停止发育。在我们的儿童中进行的生化和血液学研究在治疗期间未显示任何显著变化。鼻内治疗未观察到不良反应。我们得出结论,鼻内治疗在PP中是安全、方便且有效的,但不适用于外周性起源的PP。