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Analysis of Serum Proteome after Treatment of Osteoporosis with Anabolic or Antiresorptive Drugs

The 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 de...

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Autores principales: del Real, Alvaro, Ciordia, Sergio, Sañudo, Carolina, Garcia-Ibarbia, Carmen, Roa-Bautista, Adriel, Ocejo-Viñals, Javier G., Corrales, Fernando, Riancho, Jose A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9143104/
https://www.ncbi.nlm.nih.gov/pubmed/35629903
http://dx.doi.org/10.3390/metabo12050399
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author del Real, Alvaro
Ciordia, Sergio
Sañudo, Carolina
Garcia-Ibarbia, Carmen
Roa-Bautista, Adriel
Ocejo-Viñals, Javier G.
Corrales, Fernando
Riancho, Jose A.
author_facet del Real, Alvaro
Ciordia, Sergio
Sañudo, Carolina
Garcia-Ibarbia, Carmen
Roa-Bautista, Adriel
Ocejo-Viñals, Javier G.
Corrales, Fernando
Riancho, Jose A.
author_sort del Real, Alvaro
collection PubMed
description The 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.
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spelling pubmed-91431042022-05-29 Analysis of Serum Proteome after Treatment of Osteoporosis with Anabolic or Antiresorptive Drugs del Real, Alvaro Ciordia, Sergio Sañudo, Carolina Garcia-Ibarbia, Carmen Roa-Bautista, Adriel Ocejo-Viñals, Javier G. Corrales, Fernando Riancho, Jose A. Metabolites Article The 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. MDPI 2022-04-28 /pmc/articles/PMC9143104/ /pubmed/35629903 http://dx.doi.org/10.3390/metabo12050399 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
del Real, Alvaro
Ciordia, Sergio
Sañudo, Carolina
Garcia-Ibarbia, Carmen
Roa-Bautista, Adriel
Ocejo-Viñals, Javier G.
Corrales, Fernando
Riancho, Jose A.
Analysis of Serum Proteome after Treatment of Osteoporosis with Anabolic or Antiresorptive Drugs
title Analysis of Serum Proteome after Treatment of Osteoporosis with Anabolic or Antiresorptive Drugs
title_full Analysis of Serum Proteome after Treatment of Osteoporosis with Anabolic or Antiresorptive Drugs
title_fullStr Analysis of Serum Proteome after Treatment of Osteoporosis with Anabolic or Antiresorptive Drugs
title_full_unstemmed Analysis of Serum Proteome after Treatment of Osteoporosis with Anabolic or Antiresorptive Drugs
title_short Analysis of Serum Proteome after Treatment of Osteoporosis with Anabolic or Antiresorptive Drugs
title_sort analysis of serum proteome after treatment of osteoporosis with anabolic or antiresorptive drugs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9143104/
https://www.ncbi.nlm.nih.gov/pubmed/35629903
http://dx.doi.org/10.3390/metabo12050399
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