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dc.contributor.authorAlexander, ECen_US
dc.contributor.authorFaruqi, Den_US
dc.contributor.authorFarquhar, Ren_US
dc.contributor.authorUnadkat, Aen_US
dc.contributor.authorNg Yin, Ken_US
dc.contributor.authorHoskyns, Ren_US
dc.contributor.authorVarughese, Ren_US
dc.contributor.authorHoward, SRen_US
dc.date.accessioned2024-02-02T10:54:20Z
dc.date.available2023-11-09en_US
dc.date.issued2024-01-03en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/94409
dc.description.abstractOBJECTIVE: Hypogonadotropic hypogonadism is characterized by inadequate secretion of pituitary gonadotropins, leading to absent, partial, or arrested puberty. In males, classical treatment with testosterone promotes virilization but not testicular growth or spermatogenesis. To quantify treatment practices and efficacy, we systematically reviewed all studies investigating gonadotropins for the achievement of pubertal outcomes in males with hypogonadotropic hypogonadism. DESIGN: Systematic review and meta-analysis. METHODS: A systematic review of Medline, Embase, Global Health, and PsycINFO databases in December 2022. Risk of Bias 2.0/Risk Of Bias In Non-randomized Studies of Interventions/National Heart, Lung, and Blood Institute tools for quality appraisal. Protocol registered on PROSPERO (CRD42022381713). RESULTS: After screening 3925 abstracts, 103 studies were identified including 5328 patients from 21 countries. The average age of participants was <25 years in 45.6% (n = 47) of studies. Studies utilized human chorionic gonadotropin (hCG) (n = 93, 90.3% of studies), human menopausal gonadotropin (n = 42, 40.8%), follicle-stimulating hormone (FSH) (n = 37, 35.9%), and gonadotropin-releasing hormone (28.2% n = 29). The median reported duration of treatment/follow-up was 18 months (interquartile range 10.5-24 months). Gonadotropins induced significant increases in testicular volume, penile size, and testosterone in over 98% of analyses. Spermatogenesis rates were higher with hCG + FSH (86%, 95% confidence interval [CI] 82%-91%) as compared with hCG alone (40%, 95% CI 25%-56%). However, study heterogeneity and treatment variability were high. CONCLUSIONS: This systematic review provides convincing evidence of the efficacy of gonadotropins for pubertal induction. However, there remains substantial heterogeneity in treatment choice, dose, duration, and outcomes assessed. Formal guidelines and randomized studies are needed.en_US
dc.format.extentS1 - S11en_US
dc.languageengen_US
dc.relation.ispartofEur J Endocrinolen_US
dc.rightsThis is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
dc.subjectKallmann syndromeen_US
dc.subjectgonadotropinsen_US
dc.subjecthypogonadotropic hypogonadismen_US
dc.subjectpubertyen_US
dc.subjectspermatogenesisen_US
dc.subjectHumansen_US
dc.subjectMaleen_US
dc.subjectChorionic Gonadotropinen_US
dc.subjectFollicle Stimulating Hormoneen_US
dc.subjectGonadotropin-Releasing Hormoneen_US
dc.subjectGonadotropinsen_US
dc.subjectHypogonadismen_US
dc.subjectKlinefelter Syndromeen_US
dc.subjectSpermatogenesisen_US
dc.subjectTestisen_US
dc.subjectTestosteroneen_US
dc.subjectYoung Adulten_US
dc.titleGonadotropins for pubertal induction in males with hypogonadotropic hypogonadism: systematic review and meta-analysis.en_US
dc.typeArticle
dc.rights.holderCopyright © 2023, © The Author(s) 2023. Published by Oxford University Press on behalf of European Society of Endocrinology.
dc.identifier.doi10.1093/ejendo/lvad166en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/38128110en_US
pubs.issue1en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume190en_US
dcterms.dateAccepted2023-11-09en_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US
qmul.funderDisorders of human pubertal timing::Wellcome Trusten_US


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