Evidence map›Paper›PMID 39461874›Full record

ArticleRMD open2024

Disease response in rheumatoid arthritis across four biologic therapies associates with improvement in paraoxonase-1 activity and oxylipins.

Amir A Razmjou, Joel M Kremer, Dimitrios A Pappas, Jeffrey R Curtis, Jennifer Wang, Ani Shahbazian, David A Elashoff, Rong Guo, David Meriwether, Dawoud Sulaiman and 3 more

Abstract read
In one paragraph

Article in RMD open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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

2 citing papers in PubMed.

  1. Antioxidant Role of High-Density Lipoprotein.Antioxidants (Basel, Switzerland) · 2026
    Article
  2. Review
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.

Amir A RazmjouDepartment of Medicine, Division of Rheumatology, University of California Los Angeles, David Geffen School of Medicine, Los Angeles, California, USA arazmjou@mednet.ucla.edu.ORCID 0000-0002-5245-3998
Joel M KremerCorrona Research Foundation, Albany, New York, USA.
Dimitrios A PappasCorrona Research Foundation, Albany, New York, USA.ORCID 0000-0001-8338-027X
Jeffrey R CurtisDepartment of Medicine, Division of Rheumatology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Jennifer WangDepartment of Medicine, Division of Rheumatology, University of California Los Angeles, David Geffen School of Medicine, Los Angeles, California, USA.
Ani ShahbazianDepartment of Medicine, Division of Rheumatology, University of California Los Angeles, David Geffen School of Medicine, Los Angeles, California, USA.
David A ElashoffDivision of General Internal Medicine and Health Services Research, UCLA, Los Angeles, California, USA.
Rong GuoDivision of General Internal Medicine and Health Services Research, UCLA, Los Angeles, California, USA.
David MeriwetherDepartment of Medicine, Division of Cardiology, UCLA, Los Angeles, California, USA.
Dawoud SulaimanDepartment of Medicine, Division of Cardiology, UCLA, Los Angeles, California, USA.
Ellen O'ConnorDepartment of Medicine, Division of Cardiology, UCLA, Los Angeles, California, USA.
Srinivasa T ReddyDepartment of Medicine, Division of Cardiology, UCLA, Los Angeles, California, USA.
Christina Charles-SchoemanDepartment of Medicine, Division of Rheumatology, University of California Los Angeles, David Geffen School of Medicine, Los Angeles, California, USA.ORCID 0000-0002-1768-7019

Funding

Dysregulation of inflammation resolution as therapeutic target for IBDK01DK133666 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI David Meriwether · 2023 to 2026
$648k
NIDDK NIH HHS K01 DK133666
6 · The paper itself

Abstract

objectiveParaoxonase-1 (PON1) is a high-density lipoprotein (HDL)-associated enzyme, that has been implicated as a biomarker of cardiovascular risk in patients with rheumatoid arthritis (RA). We aimed to investigate how different biologic therapies affect levels of PON1 and oxylipins.

methods1213 adult patients with RA in the Comparative Effectiveness Registry to study Therapies for Arthritis and Inflammatory CoNditions cohort study with moderate-to-high disease activity (Clinical Disease Activity Index (CDAI) >10) who initiated a new biologic (tocilizumab (TCZ), n=296; abatacept, n=374; tumour necrosis factor inhibitors, n=427; rituximab, n=116) were followed prospectively with serum specimens analysed for PON1 activity by arylesterase (ARYL), lactonase (LAC) and PON assays at baseline and after 6 months of biologic therapy. A targeted panel of oxylipins was evaluated by liquid chromatography-mass spectrometry/mass spectrometry in a subset of patients with the lowest and highest 6-month Disease Activity Score 28 (DAS28)-C reactive protein (CRP) responses in each treatment group.

resultsPON1 activity generally increased in the entire cohort after 6 months of new biologic therapy, showing the greatest, most consistent increases in the TCZ group. Increases in all three PON1 domains associated with significant decreases in disease activity in DAS28-CRP/CDAI (p<0.05), and increases in LAC/ARYL were significantly associated with the American College of Rheumatology 20/50/70 responses (OR (95% CI) of 1.12 (1.04, 1.22) and 1.13 (1.04, 1.23), p<0.01, respectively), after controlling for other RA disease characteristics. Some oxylipins, including 12-hydroxyeicosatetraenoic acid correlated with RA disease activity measures.

conclusionImprovement in disease activity across four classes of biologics is associated with enhanced PON1 activity, which has significant implications for cardiovascular safety.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidAryldialkylphosphataseBiomarkersOxylipinsAbataceptAdultAgedAntibodies, Monoclonal, HumanizedBiological TherapyFemaleHumansMaleMiddle AgedRituximabSeverity of Illness IndexAbataceptAntibodies, Monoclonal, HumanizedAntirheumatic AgentsAryldialkylphosphataseBiomarkersOxylipinsPON1 protein, humanRituximabtocilizumabTumor Necrosis Factor Inhibitorsarthritis, rheumatoidbiological therapycardiovascular diseases

Identifiers

PMID39461874
PMCPMC11529732

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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.