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Influence of hyperbaric oxygen therapy on bone metabolism in patients with neoplasm

BACKGROUND: Hyperbaric oxygen therapy (HBOT) is useful in the treatment of complications due to radiotherapy in patients with neoplasm. Its effects on bone metabolism are unclear. In our study, we analyzed the effects of HBOT on bone remodeling in oncological patients with radiotherapy. MATERIALS AN...

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Autores principales: Salmón-González, Zaida, Anchuelo, Javier, Borregán, Juan C., Del Real, Alvaro, Riancho, José A., Valero, Carmen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Via Medica 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8241294/
https://www.ncbi.nlm.nih.gov/pubmed/34211765
http://dx.doi.org/10.5603/RPOR.a2021.0022
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author Salmón-González, Zaida
Anchuelo, Javier
Borregán, Juan C.
Del Real, Alvaro
Riancho, José A.
Valero, Carmen
author_facet Salmón-González, Zaida
Anchuelo, Javier
Borregán, Juan C.
Del Real, Alvaro
Riancho, José A.
Valero, Carmen
author_sort Salmón-González, Zaida
collection PubMed
description BACKGROUND: Hyperbaric oxygen therapy (HBOT) is useful in the treatment of complications due to radiotherapy in patients with neoplasm. Its effects on bone metabolism are unclear. In our study, we analyzed the effects of HBOT on bone remodeling in oncological patients with radiotherapy. MATERIALS AND METHODS: Prospective clinical study in 23 patients with neoplasms undergoing treatment with HBOT due to complications of radiotherapy (hemorrhagic cystitis, proctitis or radionecrosis) and 25 patients with chronic anal fissure. The average number of HBOT sessions was 20 ± 5 (100% oxygen, 2.3 atmospheres and 90 min per day). Serum levels of aminoterminal propeptide of type I collagen (P1NP), C terminal telopeptide of type I collagen (CTX), alkaline phosphatase (AP), 25hydroxyvitamin D (25-OHD), parathyroid hormone (PTH), were measured at 3 time points: T0 (before beginning HBOT), T1 (at the end of HBOT) and T2 (6 months after HBOT). RESULTS: At baseline, the patients with neoplasm have higher bone turnover than those with anal fissure. These differences were 41% in CTX (0.238 ± 0.202 ng/mL in neoplasm and 0.141 ± 0.116 ng/mL in fissure; p = 0.04), 30% for PTH (46 ± 36 pg/mL in neoplasm and 32 ± 17 pg/mL in fissure; p = 0.04) and 15% for alkaline phosphatase (80 ± 24 U/L in neoplasm and 68 ± 16 U/L in fissure; p = 0.04). In the group with neoplasm, the values of P1NP decreased 6% after HBOT (T0: 49 ± 31 ng/mL, T2: 46 ± 12 ng/mL; p = 0.03). Also, there were non-significant decreases in PTH (−34%) and CTX (−30%). CONCLUSIONS: Patients with neoplasm and complications with radiotherapy have an increase in bone remodeling that may be diminished after HBOT.
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spelling pubmed-82412942021-06-30 Influence of hyperbaric oxygen therapy on bone metabolism in patients with neoplasm Salmón-González, Zaida Anchuelo, Javier Borregán, Juan C. Del Real, Alvaro Riancho, José A. Valero, Carmen Rep Pract Oncol Radiother Research Paper BACKGROUND: Hyperbaric oxygen therapy (HBOT) is useful in the treatment of complications due to radiotherapy in patients with neoplasm. Its effects on bone metabolism are unclear. In our study, we analyzed the effects of HBOT on bone remodeling in oncological patients with radiotherapy. MATERIALS AND METHODS: Prospective clinical study in 23 patients with neoplasms undergoing treatment with HBOT due to complications of radiotherapy (hemorrhagic cystitis, proctitis or radionecrosis) and 25 patients with chronic anal fissure. The average number of HBOT sessions was 20 ± 5 (100% oxygen, 2.3 atmospheres and 90 min per day). Serum levels of aminoterminal propeptide of type I collagen (P1NP), C terminal telopeptide of type I collagen (CTX), alkaline phosphatase (AP), 25hydroxyvitamin D (25-OHD), parathyroid hormone (PTH), were measured at 3 time points: T0 (before beginning HBOT), T1 (at the end of HBOT) and T2 (6 months after HBOT). RESULTS: At baseline, the patients with neoplasm have higher bone turnover than those with anal fissure. These differences were 41% in CTX (0.238 ± 0.202 ng/mL in neoplasm and 0.141 ± 0.116 ng/mL in fissure; p = 0.04), 30% for PTH (46 ± 36 pg/mL in neoplasm and 32 ± 17 pg/mL in fissure; p = 0.04) and 15% for alkaline phosphatase (80 ± 24 U/L in neoplasm and 68 ± 16 U/L in fissure; p = 0.04). In the group with neoplasm, the values of P1NP decreased 6% after HBOT (T0: 49 ± 31 ng/mL, T2: 46 ± 12 ng/mL; p = 0.03). Also, there were non-significant decreases in PTH (−34%) and CTX (−30%). CONCLUSIONS: Patients with neoplasm and complications with radiotherapy have an increase in bone remodeling that may be diminished after HBOT. Via Medica 2021-04-14 /pmc/articles/PMC8241294/ /pubmed/34211765 http://dx.doi.org/10.5603/RPOR.a2021.0022 Text en © 2021 Greater Poland Cancer Centre https://creativecommons.org/licenses/by-nc-nd/4.0/This article is available in open access under Creative Common Attribution-Non-Commercial-No Derivatives 4.0 International (CC BY-NC-ND 4.0) license, allowing to download articles and share them with others as long as they credit the authors and the publisher, but without permission to change them in any way or use them commercially
spellingShingle Research Paper
Salmón-González, Zaida
Anchuelo, Javier
Borregán, Juan C.
Del Real, Alvaro
Riancho, José A.
Valero, Carmen
Influence of hyperbaric oxygen therapy on bone metabolism in patients with neoplasm
title Influence of hyperbaric oxygen therapy on bone metabolism in patients with neoplasm
title_full Influence of hyperbaric oxygen therapy on bone metabolism in patients with neoplasm
title_fullStr Influence of hyperbaric oxygen therapy on bone metabolism in patients with neoplasm
title_full_unstemmed Influence of hyperbaric oxygen therapy on bone metabolism in patients with neoplasm
title_short Influence of hyperbaric oxygen therapy on bone metabolism in patients with neoplasm
title_sort influence of hyperbaric oxygen therapy on bone metabolism in patients with neoplasm
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8241294/
https://www.ncbi.nlm.nih.gov/pubmed/34211765
http://dx.doi.org/10.5603/RPOR.a2021.0022
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