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Gonadotropin administration to mimic mini-puberty in hypogonadotropic males: pump or injections?
OBJECTIVE: Newborns with congenital hypogonadotropic hypogonadism (CHH) have an impaired postnatal activation of the gonadotropic axis. Substitutive therapy with recombinant gonadotropins can be proposed to mimic physiological male mini-puberty during the first months of life. The aim of this study...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bioscientifica Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10083662/ https://www.ncbi.nlm.nih.gov/pubmed/36724045 http://dx.doi.org/10.1530/EC-22-0252 |
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author | Avril, Tristan Hennocq, Quentin Lambert, Anne-Sophie Leger, Juliane Simon, Dominique Martinerie, Laetitia Bouvattier, Claire |
author_facet | Avril, Tristan Hennocq, Quentin Lambert, Anne-Sophie Leger, Juliane Simon, Dominique Martinerie, Laetitia Bouvattier, Claire |
author_sort | Avril, Tristan |
collection | PubMed |
description | OBJECTIVE: Newborns with congenital hypogonadotropic hypogonadism (CHH) have an impaired postnatal activation of the gonadotropic axis. Substitutive therapy with recombinant gonadotropins can be proposed to mimic physiological male mini-puberty during the first months of life. The aim of this study was to compare the clinical and biological efficacy of two treatment modalities of gonadotropins administration during mini-puberty in CHH neonates. DESIGN: Multicenter retrospective analytical epidemiological study comparing two treatments, pump vs injection, between 2004 and 2019. METHODS: Clinical (penile size, testis size, testicular descent) and biological parameters (serum concentrations of testosterone, anti-Müllerian hormone (AMH) and Inhibin B) were compared between the two groups by multivariate analyses. RESULTS: Thirty-five patients were included. A significantly higher increase in penile length and testosterone level was observed in the injection group compared to the pump group (+0.16 ± 0.02 mm vs +0.10 ± 0.02 mm per day, P = 0.002; and +0.04 ± 0.007 ng/mL vs +0.01 ± 0.008 ng/mL per day, P = 0.001). In both groups, significant increases in penile length and width, testosterone, AMH, and Inhibin B levels were observed, as well as improved testicular descent (odds ratio of not being in a scrotal position at the end of treatment = 0.97 (0.96; 0.99)). CONCLUSIONS: Early postnatal administration of recombinant gonadotropins in CHH boys is effective in stimulating penile growth, Sertoli cell proliferation, and testicular descent, with both treatment modalities. |
format | Online Article Text |
id | pubmed-10083662 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Bioscientifica Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-100836622023-04-11 Gonadotropin administration to mimic mini-puberty in hypogonadotropic males: pump or injections? Avril, Tristan Hennocq, Quentin Lambert, Anne-Sophie Leger, Juliane Simon, Dominique Martinerie, Laetitia Bouvattier, Claire Endocr Connect Research OBJECTIVE: Newborns with congenital hypogonadotropic hypogonadism (CHH) have an impaired postnatal activation of the gonadotropic axis. Substitutive therapy with recombinant gonadotropins can be proposed to mimic physiological male mini-puberty during the first months of life. The aim of this study was to compare the clinical and biological efficacy of two treatment modalities of gonadotropins administration during mini-puberty in CHH neonates. DESIGN: Multicenter retrospective analytical epidemiological study comparing two treatments, pump vs injection, between 2004 and 2019. METHODS: Clinical (penile size, testis size, testicular descent) and biological parameters (serum concentrations of testosterone, anti-Müllerian hormone (AMH) and Inhibin B) were compared between the two groups by multivariate analyses. RESULTS: Thirty-five patients were included. A significantly higher increase in penile length and testosterone level was observed in the injection group compared to the pump group (+0.16 ± 0.02 mm vs +0.10 ± 0.02 mm per day, P = 0.002; and +0.04 ± 0.007 ng/mL vs +0.01 ± 0.008 ng/mL per day, P = 0.001). In both groups, significant increases in penile length and width, testosterone, AMH, and Inhibin B levels were observed, as well as improved testicular descent (odds ratio of not being in a scrotal position at the end of treatment = 0.97 (0.96; 0.99)). CONCLUSIONS: Early postnatal administration of recombinant gonadotropins in CHH boys is effective in stimulating penile growth, Sertoli cell proliferation, and testicular descent, with both treatment modalities. Bioscientifica Ltd 2023-02-01 /pmc/articles/PMC10083662/ /pubmed/36724045 http://dx.doi.org/10.1530/EC-22-0252 Text en © the author(s) https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. (https://creativecommons.org/licenses/by-nc/4.0/) |
spellingShingle | Research Avril, Tristan Hennocq, Quentin Lambert, Anne-Sophie Leger, Juliane Simon, Dominique Martinerie, Laetitia Bouvattier, Claire Gonadotropin administration to mimic mini-puberty in hypogonadotropic males: pump or injections? |
title | Gonadotropin administration to mimic mini-puberty in hypogonadotropic males: pump or injections? |
title_full | Gonadotropin administration to mimic mini-puberty in hypogonadotropic males: pump or injections? |
title_fullStr | Gonadotropin administration to mimic mini-puberty in hypogonadotropic males: pump or injections? |
title_full_unstemmed | Gonadotropin administration to mimic mini-puberty in hypogonadotropic males: pump or injections? |
title_short | Gonadotropin administration to mimic mini-puberty in hypogonadotropic males: pump or injections? |
title_sort | gonadotropin administration to mimic mini-puberty in hypogonadotropic males: pump or injections? |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10083662/ https://www.ncbi.nlm.nih.gov/pubmed/36724045 http://dx.doi.org/10.1530/EC-22-0252 |
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