Quantitative analysis of the seminal plasma proteome in secondary hypogonadism

dc.contributor.authorGrande, Giuseppe
dc.contributor.authorVincenzoni, Federica
dc.contributor.authorMancini, Francesca
dc.contributor.authorBarrachina, Ferran
dc.contributor.authorGiampietro, Antonella
dc.contributor.authorCastagnola, Massimo
dc.contributor.authorUrbani, Andrea
dc.contributor.authorOliva Virgili, Rafael
dc.contributor.authorMilardi, Domenico
dc.contributor.authorPontecorvi, Alfredo
dc.date.accessioned2021-04-15T09:07:16Z
dc.date.available2021-04-15T09:07:16Z
dc.date.issued2019-12-03
dc.date.updated2021-04-15T09:07:16Z
dc.description.abstractIn the grey zone of testosterone levels between 8 and 12 nmol/L, the usefulness of therapy is controversial; as such, markers of tissue action of androgens may be helpful in adjusting clinical decisions. To better understand the effect of the hypothalamic-pituitary-testicular axis on male accessory secretion, we performed a proteomic quantitative analysis of seminal plasma in patients with secondary hypogonadism, before and after testosterone replacement therapy (TRT). Ten male patients with postsurgical hypogonadotrophic hypogonadism were enrolled in this study, and five of these patients were evaluated after testosterone treatment. Ten men with proven fertility were selected as a control group. An aliquot of seminal plasma from each individual was subjected to an in-solution digestion protocol and analyzed using an Ultimate 3000 RSLC-nano HPLC apparatus coupled to a LTQ Orbitrap Elite mass spectrometer. The label-free quantitative analysis was performed via Precursor Ions Area Detector Node. Eleven proteins were identified as decreased in hypogonadic patients versus controls, which are primarily included in hydrolase activity and protein binding activity. The comparison of the proteome before and after TRT comes about within the discovery of six increased proteins. This is the primary application of quantitative proteomics pointed to uncover a cluster of proteins reflecting an impairment not only of spermatogenesis but of the epididymal and prostate epithelial cell secretory function in male hypogonadism. The identified proteins might represent putative clinical markers valuable within the follow-up of patients with distinctive grades of male hypogonadism.
dc.format.extent13 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec696995
dc.identifier.issn2077-0383
dc.identifier.urihttps://hdl.handle.net/2445/176317
dc.language.isoeng
dc.publisherMDPI
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.3390/jcm8122128
dc.relation.ispartofJournal of Clinical Medicine, 2019, vol. 8, num. 12, p. 2128
dc.relation.urihttps://doi.org/10.3390/jcm8122128
dc.rightscc-by (c) Grande, Giuseppe et al., 2019
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Biomedicina)
dc.subject.classificationTestosterona
dc.subject.classificationProteòmica
dc.subject.classificationHipogonadisme
dc.subject.otherTestosterone
dc.subject.otherProteomics
dc.subject.otherHypogonadism
dc.titleQuantitative analysis of the seminal plasma proteome in secondary hypogonadism
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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