Oxidative and inflammatory effects of pulmonary rehabilitation in patients with bronchiectasis. A prospective, randomized study.

dc.centroFacultad de Ciencias de la Saludes_ES
dc.contributor.authorOlveira-Fuster, Casilda
dc.contributor.authorGarcía-Escobar, Eva
dc.contributor.authorDoña, Esperanza
dc.contributor.authorPalenque-Lobato, Francisco Javier
dc.contributor.authorPorras, Nuria
dc.contributor.authorDorado, Antonio
dc.contributor.authorGodoy, Ana Maria
dc.contributor.authorRubio-Martín, Elezahara
dc.contributor.authorBermúdez Silva, Francisco Javier
dc.contributor.authorRomero-Zerbo, Silvana Yanina
dc.contributor.authorRojo-Martínez, Gemma
dc.contributor.authorMartín-Valero, Rocío
dc.contributor.authorAbuín-Fernández, José
dc.contributor.authorOlveira-Fuster, Gabriel María
dc.date.accessioned2024-11-25T12:43:52Z
dc.date.available2024-11-25T12:43:52Z
dc.date.issued2020
dc.departamentoFisioterapia
dc.description.abstractBackground: systemic inflammation and oxidative stress are important factors in the pathogenesis of bronchiectasis. Pulmonary rehabilitation (PR) is recommended for bronchiectasis, but there is no data about its effect on the inflammatory and REDOX status of these patients. Aims: to investigate the effect of PR in non-cystic-fibrosis bronchiectasis (NCFB) patients, and to compare it with the effect of PR plus a hyperproteic oral nutritional supplement (PRS) enriched with beta-hydroxy-beta-methylbutyrate (HMB) on serum inflammatory and oxidative biomarkers. Materials and methods: this was an open randomized, controlled trial. Thirty individuals (65 years old or younger with a body mass index over 18.5, older than 65 years with a body mass index over 20) were recruited from September 2013 to September 2014, and randomly assigned to receive PR or PRS. Total neutrophils, and inflammatory and oxidative biomarker levels were measured at baseline, and then at 3 and 6 months. Results: in the PRS group neutrophil levels were decreased from baseline at 6 months. A significantly different fold change was found between the PR and PRS groups. In the PR group, IL-6 and adiponectin were increased by the end of the study while TNFα levels were decreased from baseline at 6 months. REDOX biomarkers remained stable throughout the study except for 8-isoprostane levels, which were increased from baseline at 6 months in both groups of patients. Conclusions: a PR program induced a pro-oxidative effect accompanied by changes in circulating inflammatory cytokine levels in NCFB patients. Our results would also suggest a possible beneficial effect of the HMB enriched supplement on neutrophil level regulation in these patients. The information provided in this study could be useful for choosing the right therapeutic approach in the management of bronchiectasis.es_ES
dc.identifier.citationOlveira C, García-Escobar E, Doña E, Palenque FJ, Porras N, Dorado A, Godoy AM, Rubio-Martín E, Bermúdez-Silva FJ, Romero-Zerbo SY, Rojo-Martínez G, Martín-Valero R, Abuín Fernández J, Olveira G. Oxidative and inflammatory effects of pulmonary rehabilitation in patients with bronchiectasis. A prospective, randomized study. Nutr Hosp 2020;37(1):6-13es_ES
dc.identifier.doi10.20960/nh.02763
dc.identifier.urihttps://hdl.handle.net/10630/35298
dc.language.isoenges_ES
dc.publisherAránes_ES
dc.rightsAttribution-NonCommercial-ShareAlike 4.0 Internacional*
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.subjectBronquiectasia - Tratamientoes_ES
dc.subjectInsuficiencia respiratoriaes_ES
dc.subject.otherBronchiectasises_ES
dc.subject.otherPulmonary rehabilitationes_ES
dc.subject.otherHMB (beta-hydroxy-beta-methylbutyrate)es_ES
dc.subject.otherOxidative stresses_ES
dc.subject.otherCytokineses_ES
dc.titleOxidative and inflammatory effects of pulmonary rehabilitation in patients with bronchiectasis. A prospective, randomized study.es_ES
dc.title.alternativeEfectos oxidativos e inflamatorios de la rehabilitación pulmonar en pacientes con bronquiectasia. Estudio prospectivo aleatorizado.es_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
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relation.isAuthorOfPublicationa1e08cff-0e42-48ca-bfdb-cbf7298e491a
relation.isAuthorOfPublication.latestForDiscovery329039ab-26c8-4de5-84b5-084686c67afe

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