Evidence map›Paper›PMID 29575818›Full record

ArticleJournal of cachexia, sarcopenia and muscle2018

Collagen-induced arthritis as an animal model of rheumatoid cachexia.

Paulo V G Alabarse, Priscila S Lora, Jordana M S Silva, Rafaela C E Santo, Eduarda C Freitas, Mayara S de Oliveira, Andrelise S Almeida, Mônica Immig, Vivian O N Teixeira, Lidiane I Filippin and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cachexia, sarcopenia and muscle, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
4.2field-weighted citation impact, top 5% of its field
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

40 citing papers in PubMed, 79 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Paulo V G AlabarseLaboratório de Doenças Autoimunes, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil.ORCID 0000-0002-9721-9302
Priscila S LoraLaboratório de Doenças Autoimunes, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil.
Jordana M S SilvaLaboratório de Doenças Autoimunes, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil.
Rafaela C E SantoLaboratório de Doenças Autoimunes, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil.
Eduarda C FreitasLaboratório de Doenças Autoimunes, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil.
Mayara S de OliveiraLaboratório de Doenças Autoimunes, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil.
Andrelise S AlmeidaLaboratório de Doenças Autoimunes, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil.
Mônica ImmigLaboratório de Doenças Autoimunes, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil.
Vivian O N TeixeiraLaboratório de Doenças Autoimunes, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil.
Lidiane I FilippinLaboratório de Doenças Autoimunes, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil.
Ricardo M XavierLaboratório de Doenças Autoimunes, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil.ORCID 0000-0001-6570-4533
Universidade Federal do Rio Grande do Sul · BRHospital de Clínicas de Porto Alegre · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRheumatoid arthritis is characterized by chronic polyarticular synovitis and presents systemic changes that impact quality of life, such as impaired muscle function, seen in up to 66% of the patients. This can progress to severely debilitating state known as rheumatoid cachexia-without loss of fat mass and body weight-for which there is little consensus in terms of diagnosis or treatment. This study aims to evaluate whether the collagen-induced arthritis (CIA) animal model also develops clinical and functional features characteristic of rheumatoid cachexia.

methodsMale DBA1/J mice were randomly divided into 2 groups: healthy animals (CO, n = 11) and CIA animals (n = 13). The clinical score and edema size, animal weight and food intake, free exploratory locomotion, grip strength, and endurance exercise performance were tested 0, 18, 35, 45, 55, and 65 days after disease induction. After euthanasia, several organs, visceral and brown fat, and muscles were dissected and weighed. Muscles were used to assess myofiber diameter. Ankle joint was used to assess arthritis severity by histological score. Statistical analysis were performed using one-way and two-way analyses of variance followed by Tukey's and Bonferroni's test or t-test of Pearson and statistical difference were assumed for a P value under 0.05.

resultsThe CIA had significantly higher arthritis scores and larger hind paw edema volumes than CO. The CIA had decreased endurance exercise performance total time (fatigue; 23, 22, 24, and 21% at 35, 45, 55, and 65 days, respectively), grip strength (27, 55, 63, 60, and 66% at 25, 35, 45, 55, and 65 days, respectively), free locomotion (43, 57, 59, and 66% at 35, 45, 55, and 65 days, respectively), and tibialis anterior and gastrocnemius muscle weight (25 and 24%, respectively) compared with CO. Sarcoplasmic ratios were also reduced in CIA (TA: 23 and GA: 22% less sarcoplasmic ratio), confirming the atrophy of skeletal muscle mass in these animals than in CO. Myofiber diameter was also reduced 45% in TA and 41% in GA in CIA when compared with the CO. Visceral and brown fat were lighter in CIA (54 and 39%, respectively) than CO group.

conclusionsThe CIA model is a valid experimental model for rheumatoid cachexia given that the clinical changes observed were similar to those described in patients with rheumatoid arthritis.

Indexed as

AnimalsArthritis, ExperimentalArthritis, RheumatoidCachexiaEdemaFootMaleMice, Inbred DBAMuscle, SkeletalCachexiaCollagen-induced arthritisMuscle lossMuscle wastingRheumatoid arthritis

Identifiers

PMID29575818
PMCPMC5989855
OpenAlexW2792509381

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

Registered trials

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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.