Evidence map›Paper›PMID 36192664›Full record

ArticleClinical rheumatology2023

Association of soluble cell adhesion molecules and lipid levels in rheumatoid arthritis patients.

Iris J Colunga-Pedraza, Dionicio A Galarza-Delgado, Natalia Guajardo-Jauregui, Jesus A Cardenas-de la Garza, Gisela Garcia-Arellano, Rosa I Arvizu-Rivera, Andrea N Garza-Cisneros, Alexis Garcia-Heredia, Mario A Balderas-Palacios, Jose R Azpiri-Lopez

Abstract read
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In one paragraph

Article in Clinical rheumatology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

10 authors at 1 institution in 1 country.

Iris J Colunga-PedrazaRheumatology Service, Internal Medicine Department, Hospital Universitario "Dr, Jose Eleuterio Gonzalez", Universidad Autonoma de Nuevo Leon, Monterrey, Nuevo Leon, Mexico.ORCID http://orcid.org/0000-0002-2786-5843
Dionicio A Galarza-DelgadoRheumatology Service, Internal Medicine Department, Hospital Universitario "Dr, Jose Eleuterio Gonzalez", Universidad Autonoma de Nuevo Leon, Monterrey, Nuevo Leon, Mexico.ORCID http://orcid.org/0000-0001-9714-2109
Natalia Guajardo-JaureguiInternal Medicine Department, Hospital Universitario "Dr, Jose Eleuterio Gonzalez", Universidad Autonoma de Nuevo Leon, Monterrey, Nuevo Leon, Mexico.ORCID http://orcid.org/0000-0003-0137-8841
Jesus A Cardenas-de la GarzaRheumatology Service, Internal Medicine Department, Hospital Universitario "Dr, Jose Eleuterio Gonzalez", Universidad Autonoma de Nuevo Leon, Monterrey, Nuevo Leon, Mexico.ORCID http://orcid.org/0000-0002-5099-0079
Gisela Garcia-ArellanoRheumatology Service, Internal Medicine Department, Hospital Universitario "Dr, Jose Eleuterio Gonzalez", Universidad Autonoma de Nuevo Leon, Monterrey, Nuevo Leon, Mexico.ORCID http://orcid.org/0000-0002-3216-3766
Rosa I Arvizu-RiveraRheumatology Service, Internal Medicine Department, Hospital Universitario "Dr, Jose Eleuterio Gonzalez", Universidad Autonoma de Nuevo Leon, Monterrey, Nuevo Leon, Mexico.ORCID http://orcid.org/0000-0002-4682-9901
Andrea N Garza-CisnerosRheumatology Service, Internal Medicine Department, Hospital Universitario "Dr, Jose Eleuterio Gonzalez", Universidad Autonoma de Nuevo Leon, Monterrey, Nuevo Leon, Mexico.
Alexis Garcia-HerediaCardiology Service, Internal Medicine Department, Hospital Universitario "Dr, Jose Eleuterio Gonzalez", Universidad Autonoma de Nuevo Leon, Francisco I. Madero Y Gonzalitos S/N, 64460, Monterrey, Nuevo Leon, Mexico.
Mario A Balderas-PalaciosRheumatology Service, Internal Medicine Department, Hospital Universitario "Dr, Jose Eleuterio Gonzalez", Universidad Autonoma de Nuevo Leon, Monterrey, Nuevo Leon, Mexico.
Jose R Azpiri-LopezCardiology Service, Internal Medicine Department, Hospital Universitario "Dr, Jose Eleuterio Gonzalez", Universidad Autonoma de Nuevo Leon, Francisco I. Madero Y Gonzalitos S/N, 64460, Monterrey, Nuevo Leon, Mexico. drazpiri@yahoo.com.ORCID http://orcid.org/0000-0002-2638-9590
Universidad Autónoma de Nuevo León · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo evaluate the relationship between soluble vascular cell adhesion molecule-1 (sVCAM-1), soluble intracellular adhesion molecule-1 (sICAM-1), and lipid levels in rheumatoid arthritis (RA) patients with and without carotid plaque (CP).

methodsCross-sectional study nested of a RA cohort. RA patients without a previous cardiovascular event or statins' therapy, aged 40-75 years were recruited at an outpatient cardio-rheumatology clinic. Carotid ultrasound was performed in all study subjects. RA patients with CP were included and matched to RA patients without CP by age, gender, and traditional cardiovascular risk factors. Blood samples were drawn at the time of recruitment to measure sVCAM-1, sICAM-1, erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and lipid levels. Correlations between cell adhesion molecules, disease activity indexes, ESR and CRP with lipid levels were assessed with Spearman's correlation coefficient (rs).

resultsWe included 71 RA patients, 37 with CP and 34 without CP. RA (n = 71) patients had a moderate negative correlation of sVCAM-1 with total cholesterol (TC) (rs =  - 0.366, p = 0.002) and low-density lipoprotein (LDL) (rs =  - 0.316, p = 0.007), and a small negative correlation with high-density lipoprotein (rs =  - 0.250, p = 0.036). ESR showed a small negative correlation with LDL (rs =  - 0.247, p = 0.038). Patients with CP had a moderate negative correlation between sVCAM and TC (rs =  - 0.405, p = 0.013). Patients without CP showed a moderate negative correlation between sVCAM with TC (rs =  - 0.364, p = 0.034) and LDL (rs =  - 0.352, p = 0.041), and sICAM with VLDL (rs =  - 0.343, p = 0.047).

conclusionsRA patients showed an inverse association of sVCAM-1 and lipid levels. More studies are needed to define the precise role of sVCAM-1 in the lipid paradox of RA.

Indexed as

Arthritis, RheumatoidCell Adhesion MoleculesC-Reactive ProteinCross-Sectional StudiesHumansIntercellular Adhesion Molecule-1LipidsVascular Cell Adhesion Molecule-1Cell Adhesion MoleculesC-Reactive ProteinIntercellular Adhesion Molecule-1LipidsVascular Cell Adhesion Molecule-1AtherosclerosisCardiovascular riskLipidsRheumatoid arthritisVascular cell adhesion molecule-1

Identifiers

PMID36192664
OpenAlexW4300861599

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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.