Evidence map›Paper›PMID 39059814›Full record

ArticleLupus science & medicine2024

Assessment of the role of high-density lipoproteins and their immunomodulatory activity in systemic lupus erythematosus immunopathology.

Julián Pérez-Ocampo, Oscar Vergara-Serpa, Carlos Jaime Velásquez-Franco, Natalia A Taborda, Lina M Yassin, Juan C Hernandez

Abstract read
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Article in Lupus science & medicine, 2024. 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
–field-weighted citation impact
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

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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.

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4 · The record

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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

6 authors.

Julián Pérez-OcampoInfettare, Facultad de medicina, Universidad Cooperativa de Colombia, Medellin, Colombia.ORCID http://orcid.org/0000-0002-7856-424X
Oscar Vergara-SerpaPostgrado de Reumatología, Universidad Pontificia Bolivariana, Medellin, Colombia.ORCID http://orcid.org/0000-0001-5009-6897
Carlos Jaime Velásquez-FrancoPostgrado de Reumatología, Universidad Pontificia Bolivariana, Medellin, Colombia.ORCID http://orcid.org/0000-0002-6498-0496
Natalia A TabordaCorporación Universitaria Remington, Medellin, Colombia.ORCID http://orcid.org/0000-0001-6085-855X
Lina M YassinCorporación Universitaria Remington, Medellin, Colombia.ORCID http://orcid.org/0000-0002-9375-0374
Juan C HernandezInfettare, Facultad de medicina, Universidad Cooperativa de Colombia, Medellin, Colombia juankhernandez@gmail.com.ORCID http://orcid.org/0000-0002-9200-5698

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo explore the potential associations between high-density lipoprotein (HDL) levels and inflammasome components in the context of systemic lupus erythematosus (SLE).

methodsA cross-sectional study was conducted. A group of 50 patients with SLE and 50 healthy controls matched by sex and similar age ranges were enrolled. Serum HDL cholesterol (HDL-C) and C reactive protein (CRP) levels were quantified. Serum cytokine levels, including IL-1β and IL-6, were determined by ELISA. The gene expression of inflammasome-related genes in peripheral blood mononuclear cells was measured by quantitative real-time PCR.

resultsHDL-C levels were lower in the patients with SLE (p<0.05), and on segregation according to disease activity, those with active SLE had the lowest HDL-C levels. Patients with SLE presented higher concentrations of the serum inflammatory cytokines IL-1β and IL-6 (p<0.0001) but similar levels of CRP to those in controls. A similar scenario was observed for the gene expression of inflammasome components, where all the evaluated markers were significantly upregulated in the SLE population. These results revealed significant negative correlations between HDL levels and disease activity, serum IL-6 and IL-1β levels and the mRNA expression of NLRP3, IL-1β and IL-18. In addition, significant positive correlations were found between disease activity and serum IL-1β and between disease activity and the mRNA expression of IL-18, and interestingly, significant positive correlations were also observed between active SLE and serum IL-1β and the mRNA expression of NLRP3.

conclusionOur results suggest that HDL is essential for SLE beyond atherosclerosis and is related to inflammation regulation, possibly mediated by inflammasome immunomodulation.

Indexed as

C-Reactive ProteinInflammasomesInterleukin-1betaLupus Erythematosus, SystemicAdultCase-Control StudiesCholesterol, HDLCross-Sectional StudiesCytokinesFemaleHumansInterleukin-6Leukocytes, MononuclearLipoproteins, HDLMaleMiddle AgedCholesterol, HDLC-Reactive ProteinCytokinesInflammasomesInterleukin-1betaInterleukin-6Lipoproteins, HDLNLR Family, Pyrin Domain-Containing 3 ProteinAtherosclerosisCytokinesInflammationLipidsSystemic Lupus Erythematosus

Identifiers

PMID39059814
PMCPMC11284925

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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.