Testosterone undecanoate maintains spermatogenic suppression induced by cyproterone acetate plus testosterone undecanoate in normal men

dc.contributor.authorHuebler, Dorisen_US
dc.contributor.authorPelusi, C.en_US
dc.contributor.authorPelusi, G.en_US
dc.contributor.authorMeriggiola, M. Cristinaen_US
dc.contributor.authorBremner, William J.en_US
dc.contributor.authorMorselli-Labate, Antonio M.en_US
dc.contributor.authorCostantino, Antoniettaen_US
dc.contributor.authorCerpolini, S.en_US
dc.contributor.authorKirsch, B.en_US
dc.contributor.authorBertaccini, Alessandroen_US
dc.date.accessioned2008-10-17T20:41:22Z
dc.date.available2008-10-17T20:41:22Z
dc.date.issued2003-12en_US
dc.description.abstractIn this study we evaluated whether testosterone undecanoate (TU), alone or combined with low dose cyproterone acetate (CPA), can maintain spermatogenic suppression induced by higher doses of CPA plus TU. Twenty-four men received for 12 wk 20 mg/d CPA plus 1000 mg/6 wk TU and then 1000 mg/8 wk TU plus 20 mg/d CPA (n = 8), 2 mg/d CPA (n = 8), or plus placebo (n = 8) for 32 wk. Blood samples, physical examinations, hormones, chemistry, hematology, semen analysis, and sexual/behavioral assessments were performed throughout the study. Sperm counts decreased to less than 1 million/ml in all subjects by wk 12, and 54% of them achieved azoospermia. Suppression of sperm counts was maintained until wk 44. Serum LH and FSH levels were suppressed by wk 12 of hormone administration and remained suppressed until wk 44. No significant changes in any biochemical parameters were detected at wk 44 in any group. There was a slight increase in total prostate volume to within the normal range at wk 44 that returned to baseline 1 yr after stopping hormone administration. In conclusion, TU alone or combined with lower doses of CPA maintains sperm suppression induced by higher dose CPA plus TU for 32 wk. This prototype regimen represents a promising male contraceptive regimen.en_US
dc.identifier.citationJ Clin Endocrinol Metab. 2003 Dec;88(12):5818-26en_US
dc.identifier.urihttp://hdl.handle.net/1773/4349
dc.language.isoen_USen_US
dc.publisherEndocrine Societyen_US
dc.subjectmale contraceptionen_US
dc.subjectreifenstein's syndromeen_US
dc.subjectcolchicineen_US
dc.subject5-alpha reductase inhibitorsen_US
dc.subjecttestosteroneen_US
dc.subjectklinefelter's syndromeen_US
dc.subjectgonadotropinsen_US
dc.subjectspermatogenesisen_US
dc.subjectandrologyen_US
dc.subject.meshLuteinizing Hormone, antagonists & inhibitors, blooden_US
dc.subject.meshDrug Synergismen_US
dc.subject.meshFollicle Stimulating Hormone, antagonists & inhibitors, blooden_US
dc.subject.meshTime Factorsen_US
dc.subject.meshSingle-Blind Methoden_US
dc.subject.meshSperm Counten_US
dc.subject.meshHumansen_US
dc.subject.meshAdulten_US
dc.subject.meshContraceptive Agents, Male, administration & dosage, pharmacologyen_US
dc.subject.meshResearch Support, Non-U.S. Gov'ten_US
dc.subject.meshMaleen_US
dc.subject.meshCyproterone Acetate, administration & dosage, pharmacologyen_US
dc.subject.meshTestosterone, analogs & derivatives, pharmacologyen_US
dc.subject.meshReference Valuesen_US
dc.subject.meshSpermatogenesis, drug effectsen_US
dc.subject.meshDose-Response Relationship, Drugen_US
dc.titleTestosterone undecanoate maintains spermatogenic suppression induced by cyproterone acetate plus testosterone undecanoate in normal menen_US
dc.typeArticleen_US

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