机构:[1]Department of Endocrine and Genetic Metabolic, Beijing Children's Hospital, Capital Medical University, Beijing 100045, China临床科室内分泌科首都医科大学附属北京儿童医院[2]Department of Adolescent Medicine, Harbin Children’s Hospital, Harbin, Heilongjiang 150010, China[3]Department of Developmental Pediatrics, The Second Hospital of Jilin University, Changchun, Jilin 130041, China[4]Department of Pediatrics, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266003, China[5]Department of Endocrinology, Shanxi Children’s Hospital, Taiyuan, Shanxi 030013, China[6]Department of Pediatrics, Tongji Hospital, TongJi Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430030, China其他科室儿科华中科技大学同济医学院附属同济医院
Background: In central precocious puberty (CPP), the pulse secretion and release of gonadotropin-releasing hormone (GnRH) are increased due to early activation of the hypothalamic-pituitary-gonadal axis, resulting in developmental abnormalities with gonadal development and appearance of secondary sexual characteristics. The CPP without organic disease is known as idiopathic CPP (ICPP). The objective of the study was to evaluate the clinical efficacy and safety of domestic leuprorelin (GnRH analog) in girls with ICPP. Methods: A total of 236 girls with ICPP diagnosed from April 2012 to January 2014 were selected and were randomized into two groups. One hundred fifty-seven girls in the test group were treated with domestic leuprorelin acetate, 79 girls in the control group were treated with imported leuprorelin acetate. They all were treated and observed for 6 months. After 6-month treatment, the percentage of children with peak luteinizing hormone (LH) <= 3.3 U/L, the percentage of children with peak LH/peak follicle stimulating hormone (FSH) ratio <0.6, the improvements of secondary sexual characteristics, gonadal development and sex hormone levels, the change of growth rate of bone age (BA) and growth velocity, and drug adverse effects between two groups were compared. Results: After the treatment, the percentage of children with a suppressed LH response to GnRH, defined as a peak LH <= 3.3 U/L, at 6 months in test and control groups were 96.80% and 96.20%, respectively, and the percentage of children with peak LH/FSH ratio <= 0.6 at 6 months in test and control groups were 93.60% and 93.70%, respectively. The sizes of breast, uterus and ovary of children and the levels of estradiol (E-2) were significantly reduced, and the growth rate of BA was also reduced. All the differences between pre- and post-treatment in each group were statistically significant (P < 0.05), but the differences of the parameters between two groups were not significant (P > 0.05). Conclusions: Domestic leuprorelin is effective and safe in the treatment of Chinese girls with ICPP. Its effectiveness and safety are comparable with imported leuprorelin.
第一作者机构:[1]Department of Endocrine and Genetic Metabolic, Beijing Children's Hospital, Capital Medical University, Beijing 100045, China
通讯作者:
通讯机构:[*1]Department of Endocrine and Genetic Metabolic, Beijing Children’s Hospital, Capital Medical University, Nan Lishi Road 56#, West District, Beijing 100045, China
推荐引用方式(GB/T 7714):
Wen-Jing Li,Chun-Xiu Gong,Mei-Jie Guo,et al.Efficacy and Safety of Domestic Leuprorelin in Girls with Idiopathic Central Precocious Puberty: A Multicenter, Randomized, Parallel, Controlled Trial[J].CHINESE MEDICAL JOURNAL.2015,128(10):1314-1320.doi:10.4103/0366-6999.156773.
APA:
Wen-Jing Li,Chun-Xiu Gong,Mei-Jie Guo,Jie Xing,Tang Li...&Feng-Ting Li.(2015).Efficacy and Safety of Domestic Leuprorelin in Girls with Idiopathic Central Precocious Puberty: A Multicenter, Randomized, Parallel, Controlled Trial.CHINESE MEDICAL JOURNAL,128,(10)
MLA:
Wen-Jing Li,et al."Efficacy and Safety of Domestic Leuprorelin in Girls with Idiopathic Central Precocious Puberty: A Multicenter, Randomized, Parallel, Controlled Trial".CHINESE MEDICAL JOURNAL 128..10(2015):1314-1320