Evidence map›Paper›PMID 34506500›Full record

Observational studyPloS one2021

Serum chemerin levels: A potential biomarker of joint inflammation in women with rheumatoid arthritis.

Fabiola Gonzalez-Ponce, Jorge I Gamez-Nava, Emilio E Perez-Guerrero, Ana M Saldaña-Cruz, Maria L Vazquez-Villegas, Juan M Ponce-Guarneros, Miguel Huerta, Xochitl Trujillo, Betsabe Contreras-Haro, Alberto D Rocha-Muñoz and 7 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Organokines in Rheumatoid Arthritis: A Critical Review.International journal of molecular sciences · 2022
    Review
  15. Article
  16. Article
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

17 authors at 3 institutions in 1 country.

Fabiola Gonzalez-PonceDepartamento de Fisiología Centro Universitario de Ciencias de la Salud, Programa de Doctorado en Farmacología, Instituto de Terapeutica Experimental y Clínica, Universidad de Guadalajara, Guadalajara, Jalisco, Mexico.
Jorge I Gamez-NavaDepartamento de Fisiología Centro Universitario de Ciencias de la Salud, Programa de Doctorado en Farmacología, Instituto de Terapeutica Experimental y Clínica, Universidad de Guadalajara, Guadalajara, Jalisco, Mexico.
Emilio E Perez-GuerreroInstituto de Investigación en Ciencias Biomédicas, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Guadalajara, Jalisco, Mexico.
Ana M Saldaña-CruzDepartamento de Fisiología Centro Universitario de Ciencias de la Salud, Programa de Doctorado en Farmacología, Instituto de Terapeutica Experimental y Clínica, Universidad de Guadalajara, Guadalajara, Jalisco, Mexico.
Maria L Vazquez-VillegasDepartamento de Salud Pública, Programa de Doctorado en Salud Publica, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Guadalajara, Jalisco, Mexico.
Juan M Ponce-GuarnerosDepartamento de Fisiología Centro Universitario de Ciencias de la Salud, Programa de Doctorado en Farmacología, Instituto de Terapeutica Experimental y Clínica, Universidad de Guadalajara, Guadalajara, Jalisco, Mexico.
Miguel HuertaCentro Universitario de Investigaciones Biomedicas, Universidad de Colima, Colima, Mexico.
Xochitl TrujilloCentro Universitario de Investigaciones Biomedicas, Universidad de Colima, Colima, Mexico.ORCID 0000-0001-7506-1674
Betsabe Contreras-HaroDivisión de Ciencias de la Salud, Departamento de Ciencias Biomédicas, Departamento Salud-Enfermedad como Proceso Individual, Centro Universitario de Tonalá, Universidad de Guadalajara, Tonalá, Jalisco México.
Alberto D Rocha-MuñozDivisión de Ciencias de la Salud, Departamento de Ciencias Biomédicas, Departamento Salud-Enfermedad como Proceso Individual, Centro Universitario de Tonalá, Universidad de Guadalajara, Tonalá, Jalisco México.
Maria O Carrillo-EscalanteDepartamento de Salud Pública, Programa de Doctorado en Salud Publica, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Guadalajara, Jalisco, Mexico.
Esther N Sanchez-RodriguezDepartamento de Fisiología Centro Universitario de Ciencias de la Salud, Programa de Doctorado en Farmacología, Instituto de Terapeutica Experimental y Clínica, Universidad de Guadalajara, Guadalajara, Jalisco, Mexico.
Eli E Gomez-RamirezDepartamento de Fisiología Centro Universitario de Ciencias de la Salud, Programa de Doctorado en Farmacología, Instituto de Terapeutica Experimental y Clínica, Universidad de Guadalajara, Guadalajara, Jalisco, Mexico.
Cesar A Nava-ValdiviaDepartamento de Microbiologia y Patologia, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Guadalajara, Jalisco, Mexico.
Ernesto G Cardona-MuñozDepartamento de Fisiología Centro Universitario de Ciencias de la Salud, Programa de Doctorado en Farmacología, Instituto de Terapeutica Experimental y Clínica, Universidad de Guadalajara, Guadalajara, Jalisco, Mexico.
Laura Gonzalez-LopezDepartamento de Fisiología Centro Universitario de Ciencias de la Salud, Programa de Doctorado en Farmacología, Instituto de Terapeutica Experimental y Clínica, Universidad de Guadalajara, Guadalajara, Jalisco, Mexico.ORCID 0000-0002-6517-6344
Research Group for the Assessment of Prognosis Biomarkers in Autoimmune Disorders
Universidad de Guadalajara · MXMexican Social Security Institute · MXUniversidad de Colima · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChemerin has a potential role in perpetuating inflammation in autoimmune diseases. Nevertheless, to date, there is no conclusive information on whether high chemerin levels increase the severity of rheumatoid arthritis (RA). Therefore, this study evaluated whether serum chemerin is a biomarker of disease activity in RA patients.

methodsStudy design: cross-sectional. The assessment included clinical and laboratory characteristics, body mass index (BMI) and fat mass. The severity of the disease activity was identified according to the DAS28-CRP index as follows: A) RA with a DAS28-CRP≤2.9 (remission/mild activity) and B) RA with a DAS28-CRP>2.9 (moderate/severe activity). Serum chemerin concentrations were measured by ELISA, and ≥103 ng/mL was considered a high level. Logistic regression analysis was applied to determine whether high chemerin levels were associated with disease activity in RA after adjusting for confounders. Multiple regression analysis was performed to identify variables associated with chemerin levels.

resultsOf 210 RA patients, 89 (42%) subjects had moderate/severe disease activity and had higher serum chemerin levels than patients with low disease activity or remission (86 ± 34 vs 73± 27; p = 0.003). Serum chemerin correlated with the number of swollen joints (r = 0.15; p = 0.03), DAS28-CRP (r = 0.22; p = 0.002), and C-reactive protein levels (r = 0.14; p = 0.04), but no correlation was observed with BMI and fat mass. In the adjusted logistic regression analysis, high chemerin levels (≥103 ng/mL) were associated with an increased risk of moderate/severe disease activity (OR: 2.76, 95% CI 1.35-5.62; p = 0.005). In the multiple regression analysis, after adjusting for potential confounders, serum chemerin levels were associated with higher DAS28-CRP (p = 0.002).

conclusionsHigher chemerin levels increased the risk of moderate and severe disease activity in RA. These results support the role of chemerin as a marker of inflammation in RA. Follow-up studies will identify if maintaining low chemerin levels can be used as a therapeutic target.

Indexed as

Severity of Illness IndexArthritis, RheumatoidBiomarkersChemokinesC-Reactive ProteinCross-Sectional StudiesFemaleHumansInflammationKnee JointMiddle AgedPrognosisBiomarkersChemokinesC-Reactive ProteinRARRES2 protein, human

Identifiers

PMID34506500
PMCPMC8432803
OpenAlexW3197797578

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.