Evidence map›Paper›PMID 32447598›Full record

ArticleClinical rheumatology2020

Cachexia in patients with rheumatoid arthritis: a cohort study.

Rafaela Ce Santo, Jordana Ms Silva, Priscila S Lora, Ana Laura D Moro, Eduarda C Freitas, Bárbara J Bartikoski, Nicole Pb Andrade, Penélope E Palominos, Vanessa Hax, Tayane M Fighera and 6 more

Abstract read
PubMed Publisher
In one paragraph

Article in Clinical rheumatology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
2.3field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 25 citations in OpenAlex.

  1. Pooled it
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  6. Observational
  7. Fly Me to the Immune: Immunonutrition in Rheumatic Diseases.Mediterranean journal of rheumatology · 2023
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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

16 authors at 5 institutions in 3 countries.

Rafaela Ce SantoHospital de Clínicas de Porto Alegre, Laboratório de Doenças Autoimunes, Porto Alegre, Brazil. rcsanto@hcpa.edu.br.ORCID https://orcid.org/0000-0002-5518-3479
Jordana Ms SilvaHospital de Clínicas de Porto Alegre, Laboratório de Doenças Autoimunes, Porto Alegre, Brazil.ORCID https://orcid.org/0000-0002-0357-4638
Priscila S LoraUniversidade do Vale do Rio dos Sinos, São Leopoldo, Brazil.ORCID https://orcid.org/0000-0002-1543-769X
Ana Laura D MoroHospital de Clínicas de Porto Alegre, Laboratório de Doenças Autoimunes, Porto Alegre, Brazil.ORCID https://orcid.org/0000-0001-5821-5467
Eduarda C FreitasHospital de Clínicas de Porto Alegre, Laboratório de Doenças Autoimunes, Porto Alegre, Brazil.ORCID https://orcid.org/0000-0002-0218-2296
Bárbara J BartikoskiHospital de Clínicas de Porto Alegre, Laboratório de Doenças Autoimunes, Porto Alegre, Brazil.
Nicole Pb AndradeHospital de Clínicas de Porto Alegre, Laboratório de Doenças Autoimunes, Porto Alegre, Brazil.ORCID https://orcid.org/0000-0003-1090-3708
Penélope E PalominosHospital de Clínicas de Porto Alegre, Laboratório de Doenças Autoimunes, Porto Alegre, Brazil.ORCID https://orcid.org/0000-0003-0132-4325
Vanessa HaxHospital de Clínicas de Porto Alegre, Laboratório de Doenças Autoimunes, Porto Alegre, Brazil.ORCID https://orcid.org/0000-0003-3240-7174
Tayane M FigheraHospital de Clínicas de Porto Alegre, Serviço de Endocrinologia, Porto Alegre, Brazil.ORCID https://orcid.org/0000-0001-7751-0197
Poli Mara SpritzerHospital de Clínicas de Porto Alegre, Serviço de Endocrinologia, Porto Alegre, Brazil.ORCID https://orcid.org/0000-0002-5204-107X
Claiton V BrenolHospital de Clínicas de Porto Alegre, Laboratório de Doenças Autoimunes, Porto Alegre, Brazil.ORCID https://orcid.org/0000-0003-0229-7912
Rafael Ms ChakrHospital de Clínicas de Porto Alegre, Laboratório de Doenças Autoimunes, Porto Alegre, Brazil.ORCID https://orcid.org/0000-0002-8677-2479
Lidiane I FilippinUniversidade La Salle, Canoas, Brazil.ORCID https://orcid.org/0000-0003-2043-6162
Joshua F BakerUniversity of Pennsylvania, Philadelphia, PA, USA.ORCID https://orcid.org/0000-0003-0170-028X
Ricardo M XavierHospital de Clínicas de Porto Alegre, Laboratório de Doenças Autoimunes, Porto Alegre, Brazil.ORCID https://orcid.org/0000-0001-6570-4533
Universidade Federal do Rio Grande do Sul · BRHospital de Clínicas de Porto Alegre · BRUniversidade do Vale do Rio dos Sinos · BRUniversidade La Salle · BRUniversity of Pennsylvania · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRheumatoid arthritis (RA) is an inflammatory disease that leads to altered body composition. The loss of lean mass with a preservation or increase in fat mass has been termed rheumatoid cachexia (RC), to contrast with classic cachexia, which is characterized by severe weight loss. There are limited data on the prevalence and progression of cachexia in RA over time, as well as on associated factors. Our aim was to determine the prevalence of cachexia and to determine associations with potential factors.

methodsThis prospective cohort study recruited consecutively patients diagnosed with RA and followed for 1 year. The assessments were performed: clinical features, body composition, and physical function. RC and classic cachexia were assessed by several established diagnostic criteria. The pairwise Student's t test, Chi-square test, and GEE were performed (accepted at p ≤ 0.05).

resultsOf 90 patients recruited, 81 completed the study. Most patients were women (88.9%), and the mean age was 56.5 ± 7.3 years. At baseline, the median DAS28-CRP was 3.0 (IQR, 1.0-3.0), 13.3-30.0% of the included patients had RC, while none met criteria for classic cachexia. The prevalence of cachexia did not change after 12 months. Disease activity status and treatment with biologic disease-modifying antirheumatic drugs were significantly associated with changes on body composition and physical function (p < 0.05).

conclusionsIn this cohort, RC was common, while classic cachexia was absent. Disease activity and use of biologic therapies were associated with changes on body composition and physical function, underscoring the importance of aiming for remission when treating RA.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidBody CompositionCachexiaCohort StudiesFemaleHumansMiddle AgedProspective StudiesAntirheumatic AgentsAdiposityCachexiaMuscleRheumatoid arthritisRheumatoid cachexia

Identifiers

PMID32447598
OpenAlexW3028487486

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.