Evidence map›Paper›PMID 38514392›Full record

ArticleRheumatology (Oxford, England)2025

Improvement of high-density lipoprotein atheroprotective properties in patients with systemic lupus erythematosus after belimumab treatment.

Anastasia-Georgia Dedemadi, Christina Gkolfinopoulou, Dimitra Nikoleri, Myrto Nikoloudaki, Hanna Ruhanen, Minna Holopainen, Reijo Käkelä, Georgia Christopoulou, Stavros Bournazos, Pantelis Constantoulakis and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

13 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Cardiac Involvement in Systemic Lupus Erythematosus.Reviews in cardiovascular medicine · 2025
    Review
  6. Article
  7. Review
  8. Review
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  12. Observational
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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

13 authors at 5 institutions in 4 countries.

Anastasia-Georgia DedemadiInstitute of Biosciences and Applications, National Center for Scientific Research "Demokritos", Agia Paraskevi, Athens, Greece.
Christina GkolfinopoulouInstitute of Biosciences and Applications, National Center for Scientific Research "Demokritos", Agia Paraskevi, Athens, Greece.
Dimitra NikoleriLaboratory of Rheumatology, Autoimmunity and Inflammation, University of Crete Medical School, Heraklion, Greece.
Myrto NikoloudakiLaboratory of Rheumatology, Autoimmunity and Inflammation, University of Crete Medical School, Heraklion, Greece.
Hanna RuhanenHelsinki University Lipidomics Unit, HiLIPID, Helsinki Institute of Life Science, HiLIFE, and Biocenter Finland, Helsinki, Finland.
Minna HolopainenHelsinki University Lipidomics Unit, HiLIPID, Helsinki Institute of Life Science, HiLIFE, and Biocenter Finland, Helsinki, Finland.
Reijo KäkeläHelsinki University Lipidomics Unit, HiLIPID, Helsinki Institute of Life Science, HiLIFE, and Biocenter Finland, Helsinki, Finland.
Georgia ChristopoulouGenotypos-Science Labs, Athens, Greece.
Stavros BournazosGenotypos-Science Labs, Athens, Greece.
Pantelis ConstantoulakisGenotypos-Science Labs, Athens, Greece.
Prodromos SidiropoulosLaboratory of Rheumatology, Autoimmunity and Inflammation, University of Crete Medical School, Heraklion, Greece.ORCID 0000-0001-9607-0326
George BertsiasLaboratory of Rheumatology, Autoimmunity and Inflammation, University of Crete Medical School, Heraklion, Greece.ORCID 0000-0001-5299-1406
Angeliki ChroniInstitute of Biosciences and Applications, National Center for Scientific Research "Demokritos", Agia Paraskevi, Athens, Greece.ORCID 0000-0003-3107-1189
University of Crete · GRGenotype (Germany) · DEUniversity of Helsinki · FINational Centre of Scientific Research "Demokritos" · GRNational and Kapodistrian University of Athens · GR

Funding

Greece and the European Union
6 · The paper itself

Abstract

objectiveChronic inflammatory diseases, like Systemic Lupus Erythematosus (SLE), carry an increased risk for atherosclerosis and cardiovascular events, accompanied by impairment of atheroprotective properties of high-density lipoprotein (HDL). In SLE, serum B cell-activating factor (BAFF), a cytokine implicated in disease progression, has been correlated with subclinical atherosclerosis. We investigated the impact of treatment with belimumab -an anti-BAFF monoclonal antibody- on HDL atheroprotective properties and composition in SLE patients.

methodsSerum samples were collected from 35 SLE patients with active disease despite conventional therapy, before and after 6-month add-on treatment with belimumab, and 26 matched healthy individuals. We measured cholesterol efflux and antioxidant capacities, paraoxonase-1 (PON1) activity, serum amyloid A1 (SAA1), myeloperoxidase (MPO) and lipid peroxidation product levels of HDL. LC-MS/MS was performed to analyse the HDL lipidome.

resultsFollowing treatment with belimumab, cholesterol efflux and antioxidant capacities of HDL were significantly increased in SLE patients and restored to levels of control subjects. HDL-associated PON1 activity was also increased, whereas lipid peroxidation products were decreased following treatment. HDL cholesterol efflux and antioxidant capacities correlated negatively with the disease activity. Changes were noted in the HDL lipidome of SLE patients following belimumab treatment, as well as between SLE patients and healthy individuals, and specific changes in lipid species correlated with functional parameters of HDL.

conclusionsHDL of SLE patients with active disease displays impaired atheroprotective properties accompanied by distinct lipidomic signatures compared with controls. Belimumab treatment may improve the HDL atheroprotective properties and modify the HDL lipidomic signature in SLE patients, thus potentially mitigating atherosclerosis development.

Indexed as

Antibodies, Monoclonal, HumanizedAtherosclerosisImmunosuppressive AgentsLipoproteins, HDLLupus Erythematosus, SystemicAdultAryldialkylphosphataseB-Cell Activating FactorCase-Control StudiesFemaleHumansLipid PeroxidationMaleMiddle AgedPeroxidaseSerum Amyloid A ProteinAntibodies, Monoclonal, HumanizedAryldialkylphosphataseB-Cell Activating FactorbelimumabImmunosuppressive AgentsLipoproteins, HDLPeroxidasePON1 protein, humanSerum Amyloid A Proteinatheroprotectionbiologicalshigh-density lipoproteinlipidomic profilesystemic lupus erythematosus

Identifiers

PMID38514392
PMCPMC11781589
OpenAlexW4393077503

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.