Evidence map›Paper›PMID 39340807›Full record

ArticleRheumatology (Oxford, England)2025

Anti-pentraxin 3 antibodies and residual disease activity in rheumatoid arthritis.

Mariangela Salvato, Francesca Frizzera, Anna Ghirardello, Antonia Calligaro, Costantino Botsios, Margherita Zen, Andrea Doria, Alessandro Giollo

Abstract 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 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

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.

  1. Review
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  4. Unveiling a novelFrontiers in medicine · 2025
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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

8 authors.

Mariangela SalvatoRheumatology Unit, Department of Medicine, University of Padova, Padova, Italy.
Francesca FrizzeraRheumatology Unit, Department of Medicine, University of Padova, Padova, Italy.
Anna GhirardelloRheumatology Unit, Department of Medicine, University of Padova, Padova, Italy.
Antonia CalligaroRheumatology Unit, Department of Medicine, University of Padova, Padova, Italy.
Costantino BotsiosRheumatology Unit, Department of Medicine, University of Padova, Padova, Italy.
Margherita ZenRheumatology Unit, Department of Medicine, University of Padova, Padova, Italy.ORCID 0000-0003-0835-1406
Andrea DoriaRheumatology Unit, Department of Medicine, University of Padova, Padova, Italy.ORCID 0000-0003-0548-4983
Alessandro GiolloRheumatology Unit, Department of Medicine, University of Padova, Padova, Italy.ORCID 0000-0001-9355-7673

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThis study quantified anti-PTX3 antibodies in the serum of seropositive and seronegative RA patients, examining their associations with disease activity and patient-reported outcome measures (PROMs).

methodsIn this cross-sectional study, RA patients diagnosed per ACR/EULAR 2010 criteria were recruited. Seronegative RA was defined as ACPA <7 kU/L. Data on demographics, clinical characteristics, medications, and PROMs were collected. Serum anti-PTX3 antibodies were measured using an in-house ELISA method. Comparative analyses were conducted with historical controls having PsA and FM.

resultsThe cohort included 83 RA patients (42 seropositive, 41 seronegative). Seropositive patients had lower anti-PTX3 antibody levels than PsA (P = 0.001) and FM (P = 0.004) controls. Seronegative patients had higher levels than seropositive ones (P = 0.032). Anti-PTX3 antibodies correlated with CDAI (r = 0.255), PtGA (r = 0.257), VAS-GH (r = -0.235), VAS-pain (r = 0.233), and HAQ (r = 0.311), but not with joint counts, inflammatory markers, or physician's global assessment. The PtGA association remained significant when adjusted for BMI, SJC28, ESR, and prednisone dosage (β = 0.206, P = 0.042). Patients with near-controlled RA (SJC28 ≤ 2, PtGA > 2) had higher anti-PTX3 levels than those with controlled disease (SJC28 ≤ 2, PtGA ≤ 2; P = 0.048). Tocilizumab or abatacept-treated patients had lower levels compared with those on TNFi or JAKi.

conclusionElevated anti-PTX3 antibodies in RA indicate residual active disease despite controlled inflammation. They may serve as a biomarker for true active disease, especially in seronegative RA patients who might be undertreated.

Indexed as

Arthritis, RheumatoidAutoantibodiesC-Reactive ProteinSerum Amyloid P-ComponentAdultAgedAntirheumatic AgentsBiomarkersCross-Sectional StudiesFemaleHumansMaleMiddle AgedPatient Reported Outcome MeasuresPentraxinsSeverity of Illness IndexAntirheumatic AgentsAutoantibodiesBiomarkersC-Reactive ProteinPentraxinsSerum Amyloid P-ComponentbiologicalCDAIDMARDspainpatient global assessmentpentraxinPTX3RA

Identifiers

PMID39340807
PMCPMC11962886

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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.