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dc.contributor.authorReal Bolt, Álvaro del es_ES
dc.contributor.authorCiordia, Sergioes_ES
dc.contributor.authorSañudo Campo, María Carolina es_ES
dc.contributor.authorGarcía Ibarbia, María del Carmen es_ES
dc.contributor.authorRoa-Bautista, Adrieles_ES
dc.contributor.authorOcejo-Viñals, Javier G.es_ES
dc.contributor.authorCorrales, Fernandoes_ES
dc.contributor.authorRiancho Moral, José Antonio es_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2023-03-20T16:33:12Z
dc.date.available2023-03-20T16:33:12Z
dc.date.issued2022es_ES
dc.identifier.issn2218-1989es_ES
dc.identifier.urihttps://hdl.handle.net/10902/28266
dc.description.abstractThe aim of the study was to explore new markers in serum proteome associated with the response to antiosteoporosis drugs, namely teriparatide and denosumab. We obtained serum samples from 14 patients with osteoporosis, both at baseline and after 6 months of treatment with teriparatide (n = 10) or denosumab (n = 4). Samples were analyzed by nanoliquid chromatography coupled to high-resolution mass spectrometry on a QTOF 5600 (SCIEX) apparatus. The spectrometry data were analyzed with Mascot against the UniProtKB base and then several quality-control filters were applied for the identification of peptides (false discovery rate, FDR q < 0.02) and their quantification (FDR q < 0.05). In the group treated with teriparatide, 28 proteins were identified with significant differences before and after treatment. A pathway analysis by using the Reactome database revealed significant enrichment in the Insulin Like Growth Factor 1 (IGF-I) (FDR q 4 × 10-²) and innate immune system (FDR q 2 × 10-³) pathways. Among patients treated with denosumab, we observed significant differences in the levels of 10 proteins, which were also enriched in the pathways related to the innate immune system (FDR q 3 × 10-²). These results suggest that the innate immune system may be involved in the response to antiosteoporosis drugs.es_ES
dc.description.sponsorshipFunding: Supported by grants from FEIOMM (Grant No.17/0025) and ProteoRed-ISCIII. Acknowledgments: Alvaro del Real received support by the postdoctoral grant Augusto Gonzalez de Linares of the University of Cantabria.es_ES
dc.format.extent11 p.es_ES
dc.language.isoenges_ES
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)es_ES
dc.rightsAttribution 4.0 International*
dc.rights© 2022 by the authorses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceMetabolites 2022, 12, 399es_ES
dc.subject.otherProteomees_ES
dc.subject.otherOsteoporosises_ES
dc.subject.otherBonees_ES
dc.subject.otherAntiresorptive drugses_ES
dc.subject.otherTeriparatidees_ES
dc.titleAnalysis of serum proteome after treatment of osteoporosis with anabolic or antiresorptive drugses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.3390/metabo12050399es_ES
dc.type.versionpublishedVersiones_ES


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Attribution 4.0 InternationalExcepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International