Literature DB >> 29931143

Oxandrolone Treatment Results in an Increased Risk of Gonadarche in Prepubertal Boys With Klinefelter Syndrome.

Shanlee M Davis1,2, Najiba Lahlou3,4, Matthew Cox-Martin5, Karen Kowal6,7, Philip S Zeitler1,2, Judith L Ross6,7.   

Abstract

Context: Klinefelter syndrome (KS) is a common genetic condition in which males have an extra X chromosome. KS is associated with testosterone deficiency, neurodevelopmental delays, and cardiometabolic disorders. There has been recent interest in prepubertal androgen treatment; however, the effects on puberty and gonadal function are unknown. Objective: To compare onset of puberty and testicular function in prepubertal boys treated with 2 years of oxandrolone (Ox) vs placebo (Pl). Design: Double-blind, randomized, controlled trial. Setting: Single tertiary care referral center. Participants: Eighty prepubertal boys with KS; mean age: 8.0 ± 2.2 years (range: 4 to 12). Interventions: Ox 0.05 mg/kg vs identical-appearing Pl capsule given for 2 years. Outcome Measures: Onset of gonadarche (testicular volume ≥4 mL) and onset of pubarche (Tanner 2 pubic hair); change in testicular hormone concentrations.
Results: Ox-treated group had 20.5 times higher odds of reaching gonadarche (OR 95% CI: 6.5, 77.8) and 28.1 times higher odds of reaching pubarche (OR 95% CI: 8.8, 110.4) during the 2-year study period after adjusting for baseline age. Gonadarche and pubarche both occurred at a younger age in the Ox group (gonadarche: 9.8 ± 1.5 vs 12.1 ± 1.0 years, P < 0.001; pubarche: 10.2 ± 1.1 vs 11.6 ± 1.3 years, P = 0.02). Serum concentrations of testicular hormones and gonadotropins were not different between groups. Conclusions: Two years of Ox treatment in prepubertal boys with KS results in an increased risk of early gonadarche, on average 2 years earlier than in Pl-treated boys. Ox did not affect serum concentrations of testicular hormones.

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Year:  2018        PMID: 29931143      PMCID: PMC6126887          DOI: 10.1210/jc.2018-00682

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  21 in total

1.  Prenatal and postnatal prevalence of Klinefelter syndrome: a national registry study.

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2.  A double-blind, placebo-controlled comparison of letrozole to oxandrolone effects upon growth and puberty of children with constitutional delay of puberty and idiopathic short stature.

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4.  Positive effects of short course androgen therapy on the neurodevelopmental outcome in boys with 47,XXY syndrome at 36 and 72 months of age.

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5.  Androgen Treatment Effects on Motor Function, Cognition, and Behavior in Boys with Klinefelter Syndrome.

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Review 7.  Advances in the Interdisciplinary Care of Children with Klinefelter Syndrome.

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Review 8.  The anabolic androgenic steroid oxandrolone in the treatment of wasting and catabolic disorders: review of efficacy and safety.

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Review 9.  Pubertal timing in girls and depression: a systematic review.

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10.  Etiology and therapeutic outcomes of children with gonadotropin-independent precocious puberty.

Authors:  Eungu Kang; Ja Hyang Cho; Jin-Ho Choi; Han-Wook Yoo
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Review 1.  Morbidity in Klinefelter syndrome and the effect of testosterone treatment.

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2.  Sex chromosome aneuploidies in 2020-The state of care and research in the world.

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Journal:  Am J Med Genet C Semin Med Genet       Date:  2020-06-04       Impact factor: 3.908

Review 3.  Effects of the Timing of Sex-Steroid Exposure in Adolescence on Adult Health Outcomes.

Authors:  Yee-Ming Chan; Amalia Feld; Elfa Jonsdottir-Lewis
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Review 4.  Androgen Treatment in Adolescent Males With Hypogonadism.

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5.  Fast and Sensitive Screening of Oxandrolone and Its Major Metabolite 17-Epi-Oxandrolone in Human Urine by UHPLC-MS/MS with On-Line SPE Sample Pretreatment.

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Journal:  Molecules       Date:  2021-01-18       Impact factor: 4.411

6.  Cortical Bone Mass is Low in Boys with Klinefelter Syndrome and Improves with Oxandrolone.

Authors:  Maria G Vogiatzi; Shanlee M Davis; Judith L Ross
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7.  Attenuated androgen discontinuation in patients with hereditary angioedema: a commented case series.

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Review 8.  Recent advancement in the treatment of boys and adolescents with hypogonadism.

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  8 in total

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