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KMID : 1036920130180040173
Annals of Pediatric Endocrinology & Metabolism
2013 Volume.18 No. 4 p.173 ~ p.178
Multicenter clinical trial of leuprolide acetate depot (Luphere depot 3.75 mg) for efficacy and safety in girls with central precocious puberty
Kim You-Jin

Lee Hae-Sang
Lee Young-Jun
Lim Jung-Sub
Kim Se-Young
Kim Eun-Young
Jin Dong-Kyu
Hwang Il-Tae
Hwang Jin-Soon
Abstract
Purpose: We evaluated the efficacy, safety and psychological aspect of monthly administrations of the gonadotropin-releasing hormone agonists (GnRHa), leuprolide acetate depot (Luphere depot 3.75 mg), in patients with precocious puberty.

Methods: A total of 54 girls with central precocious puberty were administered with leuprolide acetate (Luphere depot 3.75 mg) every four weeks over 24 weeks. We evaluated the percentage of children exhibiting a suppressed luteinizing hormone (LH) response to GnRH (LH peak¡Â3 IU/L), peak LH/follicle stimulating hormone (FSH) ratio of GnRH stimulation test less than 1, change in bone age/chronologic age ratio, change in the Tanner stage and change in eating habit and psychological aspect.

Results: (1) The percentage of children exhibiting a suppressed LH response to GnRH, defined as an LH peak¡Â3 IU/L at 24 weeks was 96.3 % (52/54). (2) The percentage of children exhibiting peak LH/FSH ratio<1 at 24 weeks of the study was 94.4 % (51/54). (3) The ratio of bone age and chronological age significantly declined from 1.27¡¾0.07 to 1.24¡¾0.01 after the 6 months of the study. (4) The mean Tanner stage manifested a significant change 2.3¡¾0.48 at baseline, down to 1.70¡¾0.61 at 24 weeks. (5) Based on the questionnaires, the score for eating habits showed a significant change from the baseline 34.0¡¾6.8 to 31.3¡¾6.8. (6) The psychological assessment did not exhibit a significant difference except with scores for sociability, problem behavior total score and other problems.

Conclusion: The leuprolide 3.75 mg (Luphere depot) is useful and safety for treating children with central precocious puberty.
KEYWORD
Leuprolide acetate, Central precocious puberty, Treatment outcome
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