Evidence map›Paper›PMID 34477989›Full record

ArticleClinical rheumatology2022

Increased plasma levels of CCL20 in peripheral blood of rheumatoid arthritis patients and its association with clinical and laboratory parameters.

Mehran Pournazari, Parisa Feizollahi, Seyed Askar Roghani, Shirin Assar, Parviz Soufivand, Bijan Soleymani, Fariborz Bahrehmand, Zahra Mohammadi Kish, Mahdi Taghadosi

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Article in Clinical rheumatology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

4 citing papers in PubMed, 9 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

9 authors at 1 institution in 1 country.

Mehran Pournazari *Clinical Research Development Center, Imam Reza Hospital, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Parisa Feizollahi *Student Research Committee, Medical School, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Seyed Askar RoghaniImmunology Department, Faculty of Medicine, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Shirin AssarClinical Research Development Center, Imam Reza Hospital, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Parviz SoufivandClinical Research Development Center, Imam Reza Hospital, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Bijan SoleymaniMedical Biology Research Center, Health Technology Institute, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Fariborz BahrehmandMedical Biology Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Zahra Mohammadi KishMedical Biology Research Center, Health Technology Institute, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Mahdi TaghadosiDepartment of Immunology, School of Medicine, Kermanshah University of Medical Sciences, Kermanshah, Iran. mtaghad@gmail.com.ORCID http://orcid.org/0000-0002-3516-0130
Kermanshah University of Medical Sciences · IR

Funding

Kermanshah University of Medical Sciences 3010723
6 · The paper itself

Abstract

introductionRheumatoid arthritis (RA) is a systemic autoimmune disease that primarily affects small joints. The impaired chemokine and cytokine responses are essential pathological mechanisms for the RA clinical presentation. Given the role of chemokines and inflammatory reactions in RA pathogenesis, we evaluate the association between the plasma concentration of CCL20 with the clinical and laboratory parameters in newly diagnosed RA patients. MATERIAL AND

methodsForty-five newly diagnosed RA patients and forty-five healthy subjects were enrolled in this study. The plasma levels of CCL20, rheumatoid factor, and anti-citrullinated peptide antibodies were measured using the enzyme-linked immunosorbent assay (ELISA) technique.

resultThe plasma levels of CCL20 were increased significantly in RA patients compared to the healthy controls (p < 0.0001). There was a positive correlation between CCL20 and RF, anti-CCP, ESR, and DAS-28 (p < 0.0001, r = 0.669; p < 0.015, r = 0.358; p < 0.0001, r = 0.586; p < 0.0001, r = 0.769).

conclusionThe increased plasma levels of CCL20 in newly diagnosed RA patients may contribute to RA pathogenesis, and it is in association with clinical and laboratory parameters. Key Points • CCL20 has a contribution to the early phase of RA.

Indexed as

Arthritis, RheumatoidLaboratoriesAutoantibodiesBiomarkersChemokine CCL20Enzyme-Linked Immunosorbent AssayHumansPeptides, CyclicRheumatoid FactorAutoantibodiesBiomarkersCCL20 protein, humanChemokine CCL20Peptides, CyclicRheumatoid FactorAnti-CCPCCL20ChemokinesDAS28RFRheumatoid arthritis

Identifiers

PMID34477989
OpenAlexW3198140360

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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.