leuprolide and Brain-Diseases

leuprolide has been researched along with Brain-Diseases* in 4 studies

Other Studies

4 other study(ies) available for leuprolide and Brain-Diseases

ArticleYear
Near final height after GnRH agonist treatment in central precocious puberty.
    Journal of pediatric endocrinology & metabolism : JPEM, 2000, Volume: 13 Suppl 1

    The impact of treatment of central precocious puberty (CPP) with gonadotropin-releasing hormone agonists (GnRHa) on final height remains controversial. We analyzed the long term results of 23 girls with CPP treated with triptorelin or leuprolide. Their "near final height" (NFH) assessed at a bone age of at least 14 years and expressed as SDS, was compared either with predicted height before treatment (PAH) or with parental height (TH). We also compared NFH of 12 girls treated before 8 years of age (7.0 +/- 0.5 yr) with NFH of 11 girls treated after 8 years old (8.5 +/- 0.3 yr). The NFH of the 23 girls (-0.9 +/- 1.0 SDS) was not different either from PAH (-0.85 +/- 1.5 SDS) or from TH (-0.5 +/0.6 SDS). Earlier treated girls reached a NFH (-0.97 +/- 1.0 SDS) not different from later treated girls (-0.91 +/- 1.0 SDS; p = ns) and both groups reached parental height (NFH - TH = -0.44 +/- 1 and -0.09 +/- 0.83 SDS, respectively). In conclusion, our patients, treated either earlier or later, reached a near final height comparable to predicted height and familial target; however, these results might still improve further because the girls have not yet reached their final adult height.

    Topics: Body Height; Bone Development; Brain Diseases; Child; Female; Gonadotropin-Releasing Hormone; Humans; Leuprolide; Puberty, Precocious; Triptorelin Pamoate

2000
Precocious puberty and body composition: effects of GnRH analog treatment.
    Journal of pediatric endocrinology & metabolism : JPEM, 2000, Volume: 13 Suppl 1

    Body composition changes with age and sex differences become significant only after puberty. Boys and girls before the age of 8 yr do not differ in fat, lean or bone mineral mass. Hormonal influences during pubertal development determine the physiological adult male and female body composition phenotype.. The aim of our study was to evaluate body composition changes due to central precocious puberty (PP) and the specific effects of therapy on these modifications.. Sixteen patients (14 girls, 2 boys) were included in the study. They were diagnosed as affected by idiopathic PP according to standard hormonal and clinical criteria; anatomic alterations of hypothalamus-hypophysis region were excluded by MRI. Mean age at diagnosis was 5.9 +/- 1.9 yr. All patients received GnRH analog (Leuprolide or Triptorelin) treatment subcutaneously every 4 weeks for at least 1 yr. Mean period of treatment was 3.4 +/- 1.9 yr. Standard anthropometry and body composition analysis were performed at baseline and every 6-12 months. A group of healthy subjects with normal timing of puberty was matched (for age or for pubertal stage) served as the control group (CA or CP, respectively).. Patients with PP showed at baseline a significant increase of BMI and relative body weight; lean and fat compartments were also increased but not significantly. During treatment, the PP group showed increased fat mass compared to CA (p<0.05), while no difference was found between PP and CP. Lean mass was similar to CA but lower than in CP (p<0.05). During treatment a significant increase in lean mass (both as total as well as limb mass) was observed. After stopping treatment there was no difference between PP and CP, except for lower lean mass (p<0.04).. When puberty occurs precociously, lean and fat mass are not significantly different from age-matched control subjects. Data collected during treatment confirm a shortening of prepubertal lean mass development and the block of further lean mass development due to puberty itself, while fat mass accumulation continues. The net result of these modifications determines a typical body composition pattern in PP patients, after the end of therapy: lean mass is reduced by a shortening of the prepubertal growing period and by the "menopausal effect" of treatment itself. Fat mass is increased as a consequence of therapy and could lead to future obesity.

    Topics: Adipose Tissue; Anthropometry; Body Composition; Body Mass Index; Body Weight; Brain Diseases; Child, Preschool; Female; Gonadotropin-Releasing Hormone; Humans; Leuprolide; Male; Puberty, Precocious; Triptorelin Pamoate

2000
[Seizure exacerbation by the use of leuprorelin acetate for treatment of central precocious puberty in a female patient with symptomatic localization-related epilepsy].
    No to hattatsu = Brain and development, 1999, Volume: 31, Issue:5

    Topics: Brain Diseases; Child; Epilepsies, Partial; Female; Humans; Leuprolide; Progesterone; Puberty, Precocious; Recurrence

1999
Leuprolide treatment of sexual aggression in a patient with Dementia and the Klüver-Bucy syndrome.
    Clinical neuropharmacology, 1995, Volume: 18, Issue:5

    A patient with dementia and features of the Klüver-Bucy syndrome was treated for verbal, physical, and sexually aggressive behavior disturbances. Propranolol was effective in controlling verbal and physical aggression but not sexually aggressive and inappropriate behaviors. The latter responded completely to treatment with leuprolide. The differential response to these treatments suggests that two basic forms of aggressive behavior in demented men can be identified and treated with relative specificity.

    Topics: Adult; Aggression; Brain Diseases; Dementia; Humans; Leuprolide; Male; Sexual Behavior

1995