1999
DOI: 10.1159/000023413
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Auxological and Biochemical Evaluation of Pubertal Suppression with the GnRH Agonist Leuprolide Acetate in Early and Precocious Puberty

Abstract: We studied the auxological effects of treatment with the GnRH agonist leuprolide acetate (Lucrin®) at 3.75 mg/ 28 days in 38 children with early or precocious puberty. We present our newly developed scoring system, the Puberty Suppression Score (PSS), in which clinical and biochemical parameters determine whether suppression was effective. Leuprolide acetate suppressed pubertal development in the majority of cases. During treatment there was a significant correlation between the number of times that… Show more

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Cited by 40 publications
(21 citation statements)
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“…According to some reports, adult height after the GnRHa treatment increases although there are some different effects in number13,14,15,16). In our study, pretreatment mean BA was 1.9 years advanced compare to mean CA.…”
Section: Discussionsupporting
confidence: 42%
“…According to some reports, adult height after the GnRHa treatment increases although there are some different effects in number13,14,15,16). In our study, pretreatment mean BA was 1.9 years advanced compare to mean CA.…”
Section: Discussionsupporting
confidence: 42%
“…Clinical scoring systems have been devised in an attempt to standardize assessment of CPP patients on therapy, 16 but most continue to rely on subjective measures such as change in bone age. 10 Although careful clinical assessment is crucial in follow-up of these patients, an objective and prompt laboratory measure of treatment success or failure is needed.…”
Section: Discussionmentioning
confidence: 99%
“…The inhibition of gonadotropin secretion was checked the morning after the second overnight profile by a GnRH agonist test, as follows: 0.5 mg (0.5 ml) of leuprorelide acetate was injected subcutaneously, and after 3 h, a blood sample was taken for determination of LH, FSH and testosterone levels [29, 30]. In the 4 boys in whom overnight profiles were not performed, fasting IGF-I and IGFBP-3 levels and a GnRH agonist test were performed during the second visit, after 3 months of GnRHa treatment.…”
Section: Methodsmentioning
confidence: 99%