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Arthritis induces early bone high turnover, structural degradation and mechanical weakness

dc.contributor.authorVidal, Bruno
dc.contributor.authorCascão, Rita
dc.contributor.authorVale, Ana Catarina
dc.contributor.authorCavaleiro, Inês
dc.contributor.authorVaz, Maria Fátima
dc.contributor.authorBrito, José Américo Almeida
dc.contributor.authorCanhão, Helena
dc.contributor.authorFonseca, João Eurico
dc.date.accessioned2017-05-29T10:14:20Z
dc.date.available2017-05-29T10:14:20Z
dc.date.issued2015-01
dc.description.abstractBACKGROUND: We have previously found in the chronic SKG mouse model of arthritis that long standing (5 and 8 months) inflammation directly leads to high collagen bone turnover, disorganization of the collagen network, disturbed bone microstructure and degradation of bone biomechanical properties. The main goal of the present work was to study the effects of the first days of the inflammatory process on the microarchitecture and mechanical properties of bone. METHODS: Twenty eight Wistar adjuvant-induced arthritis (AIA) rats were monitored during 22 days after disease induction for the inflammatory score, ankle perimeter and body weight. Healthy non-arthritic rats were used as controls for compar-ison. After 22 days of disease progression rats were sacrificed and bone samples were collected for histomorphometrical, energy dispersive X-ray spectroscopical analysis and 3-point bending. Blood samples were also collected for bone turnover markers. RESULTS: AIA rats had an increased bone turnover (as inferred from increased P1NP and CTX1, p = 0.0010 and p = 0.0002, respectively) and this was paralleled by a decreased mineral content (calcium p = 0.0046 and phos-phorus p = 0.0046). Histomorphometry showed a lower trabecular thickness (p = 0.0002) and bone volume (p = 0.0003) and higher trabecular sepa-ration (p = 0.0009) in the arthritic group as compared with controls. In addition, bone mechanical tests showed evidence of fragility as depicted by diminished values of yield stress and ultimate fracture point (p = 0.0061 and p = 0.0279, re-spectively) in the arthritic group. CONCLUSIONS: We have shown in an AIA rat model that arthritis induc-es early bone high turnover, structural degradation, mineral loss and mechanical weakness.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationVidal B, Cascão R, Vale AC, Cavaleiro I, Vaz MF, Brito JAA, et al. (2015) Arthritis induces early bone high turnover, structural degradation and mechanical weakness. PLoS ONE 10(1): e0117100. doi:10.1371/journal.pone.0117100pt_PT
dc.identifier.doi10.1371/journal.pone.0117100pt_PT
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/10400.26/18412
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherPLOSpt_PT
dc.relationHOW EARLY INFLAMMATORY EVENTS AFFECT BONE NANO-PROPERTIES AT THE ONSET OF RHEUMATOID ARTHRITIS
dc.relation.publisherversionhttps://doi.org/10.1371/journal.pone.0117100pt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectArthritispt_PT
dc.subjectBonept_PT
dc.titleArthritis induces early bone high turnover, structural degradation and mechanical weaknesspt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.awardTitleHOW EARLY INFLAMMATORY EVENTS AFFECT BONE NANO-PROPERTIES AT THE ONSET OF RHEUMATOID ARTHRITIS
oaire.awardURIinfo:eu-repo/grantAgreement/FCT//SFRH%2FBD%2F81527%2F2011/PT
oaire.citation.startPagee0117100pt_PT
oaire.citation.titlePLoS ONEpt_PT
oaire.citation.volume10(1)pt_PT
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
relation.isProjectOfPublication90c713fe-6a97-4763-891b-278974c12ba2
relation.isProjectOfPublication.latestForDiscovery90c713fe-6a97-4763-891b-278974c12ba2

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