Evidence map›Paper›PMID 25617902›Full record

ArticlePloS one2015

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

Bruno Vidal, Rita Cascão, Ana Catarina Vale, Inês Cavaleiro, Maria Fátima Vaz, José Américo Almeida Brito, Helena Canhão, João Eurico Fonseca

Erratum issuedAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Bruno VidalInstituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Lisbon, Portugal.
Rita CascãoInstituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Lisbon, Portugal.
Ana Catarina ValeInstituto de Ciência e Engenharia de Materiais e Superfícies, Instituto Superior Técnico, University of Lisbon, Lisbon, Portugal.
Inês CavaleiroInstituto Superior de Ciências da Saúde Egas Moniz-Campus Universitário, Quinta da Granja, Caparica, Portugal.
Maria Fátima VazInstituto de Ciência e Engenharia de Materiais e Superfícies, Instituto Superior Técnico, University of Lisbon, Lisbon, Portugal; Departamento de Engenharia Mecânica, Instituto Superior Técnico, UL, Lisbon, Portugal.
José Américo Almeida BritoInstituto Superior de Ciências da Saúde Egas Moniz-Campus Universitário, Quinta da Granja, Caparica, Portugal.
Helena CanhãoInstituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Lisbon, Portugal; Rheumatology Department, Lisbon Academic Medical Centre, Lisbon, Portugal.
João Eurico FonsecaInstituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Lisbon, Portugal; Rheumatology Department, Lisbon Academic Medical Centre, Lisbon, Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe 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.

methodsTwenty 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.

resultsAIA 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.

conclusionsWe have shown in an AIA rat model that arthritis induc-es early bone high turnover, structural degradation, mineral loss and mechanical weak-ness.

Indexed as

Bone RemodelingMechanical PhenomenaAnimalsArthritis, ExperimentalBiomarkersBiomechanical PhenomenaBone DensityFemaleLumbar VertebraeRatsRats, WistarBiomarkers

Identifiers

PMID25617902
PMCPMC4305284

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.