Evidence map›Paper›PMID 39423147›Full record

ArticleRheumatology (Oxford, England)2025

ANA-positive versus ANA-negative Antiphospholipid Antibody-positive Patients: Results from the Antiphospholipid Syndrome Alliance for Clinical Trials and International Networking (APS ACTION) Clinical Database and Repository ("Registry").

Irene Cecchi, Massimo Radin, Silvia Grazietta Foddai, Alice Barinotti, Danieli Andrade, Maria G Tektonidou, Vittorio Pengo, Guillermo Ruiz-Irastorza, H Michael Belmont, Chary Lopez Pedrera and 18 more

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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Antiphospholipid Syndrome and the Kidney.Kidney international reports · 2025
    Review
  6. 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

28 authors.

Irene CecchiUniversity Center of Excellence on Nephrologic, Rheumatologic and Rare Diseases (ERK-Net, ERN-Reconnect and RITA-ERN Member) with Nephrology and Dialysis Unit and Center of Immuno-Rheumatology and Rare Diseases (CMID), Coordinating Center of the Interregional Network for Rare Diseases of Piedmont and Aosta Valley, San Giovanni Bosco Hub Hospital, Turin, Italy.
Massimo RadinUniversity Center of Excellence on Nephrologic, Rheumatologic and Rare Diseases (ERK-Net, ERN-Reconnect and RITA-ERN Member) with Nephrology and Dialysis Unit and Center of Immuno-Rheumatology and Rare Diseases (CMID), Coordinating Center of the Interregional Network for Rare Diseases of Piedmont and Aosta Valley, San Giovanni Bosco Hub Hospital, Turin, Italy.ORCID 0000-0003-1941-2606
Silvia Grazietta FoddaiUniversity Center of Excellence on Nephrologic, Rheumatologic and Rare Diseases (ERK-Net, ERN-Reconnect and RITA-ERN Member) with Nephrology and Dialysis Unit and Center of Immuno-Rheumatology and Rare Diseases (CMID), Coordinating Center of the Interregional Network for Rare Diseases of Piedmont and Aosta Valley, San Giovanni Bosco Hub Hospital, Turin, Italy.
Alice BarinottiUniversity Center of Excellence on Nephrologic, Rheumatologic and Rare Diseases (ERK-Net, ERN-Reconnect and RITA-ERN Member) with Nephrology and Dialysis Unit and Center of Immuno-Rheumatology and Rare Diseases (CMID), Coordinating Center of the Interregional Network for Rare Diseases of Piedmont and Aosta Valley, San Giovanni Bosco Hub Hospital, Turin, Italy.
Danieli AndradeUniversity of São Paulo, São Paulo, Brazil.ORCID 0000-0002-0381-1808
Maria G TektonidouNational and Kapodistrian University of Athens, Athens, Greece.ORCID 0000-0003-2238-0975
Vittorio PengoSenior Scientist, University of Padova, Italy.ORCID 0000-0003-2064-6071
Guillermo Ruiz-IrastorzaAutoinmune Diseases Research Unit, Biobizkaia Health Research Institute, UPV/EHU, Barakaldo, Spain.ORCID 0000-0001-7788-1043
H Michael BelmontNew York University Langone Medical Center, New York, NY, USA.ORCID 0000-0003-3389-2976
Chary Lopez PedreraRheumatology Service/Department of Medical and Surgical Sciences, Maimonides Institute for Research in Biomedicine of Cordoba (IMIBIC)/ Reina Sofia University Hospital/ University of Cordoba, Córdoba, Spain.
Paul R FortinCentre ARThrite-CHU de Québec - Université Laval, Quebec, QC, Canada.
Maria GerosaUniversity of Milan, Milan, Italy.ORCID 0000-0001-5241-5847
Guilherme de JesúsUniversidade do Estado do Rio de Janeiro, Rio de Janeiro, Brazil.
Tatsuya AtsumiHokkaido University Hospital, Sapporo, Japan.
Lanlan JiPeking University First Hospital, Beijing, China.ORCID 0000-0001-9620-8882
Maria EfthymiouUniversity College London, London, UK.
D Ware BranchUniversity of Utah and Intermountain Healthcare, Salt Lake City, UT, USA.
Cecilia NalliUniversity of Brescia, Brescia, Italy.
Esther Rodriguez-AlmarazHospital Universitario, 12 de Octubre, Madrid, Spain.ORCID 0000-0003-0839-5644
Michelle PetriJohns Hopkins University School of Medicine, Baltimore, MD, USA.
Ricard CerveraDepartment of Autoimmune Diseases, Hospital Clínic, IDIBAPS, University of Barcelona, Barcelona, Catalonia,Spain.ORCID 0000-0001-6085-492X
Jason S KnightUniversity of Michigan, Ann Arbor, MI, USA.
Bahar Artim-EsenIstanbul University School of Medicine, Istanbul, Turkey.
Rohan WillisUniversity of Texas Medical Branch, Galveston, TX, USA.
Maria Laura BertolacciniSchool of Cardiovascular & Metabolic Medicine & Sciences, King's College London, London, UK.
Hannah CohenUniversity College London, London, UK.ORCID 0000-0003-2032-390X
Doruk ErkanBarbara Volcker Center for Women and Rheumatic Disease, Hospital for Special Surgery, Weill Cornell Medicine, New York, NY, USA.
Savino SciasciaUniversity Center of Excellence on Nephrologic, Rheumatologic and Rare Diseases (ERK-Net, ERN-Reconnect and RITA-ERN Member) with Nephrology and Dialysis Unit and Center of Immuno-Rheumatology and Rare Diseases (CMID), Coordinating Center of the Interregional Network for Rare Diseases of Piedmont and Aosta Valley, San Giovanni Bosco Hub Hospital, Turin, Italy.ORCID 0000-0003-1266-9441

Funding

Clinical and Translational Science AwardUL1TR001873 · NCATS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI REILLY, MUREDACH P · 2016 to 2025
$99.0M
Clinical and Translational Science CenterUL1TR000457 · NCATS · WEILL MEDICAL COLL OF CORNELL UNIV · PI IMPERATO-MCGINLEY, JULIANNE L · 2012 to 2016
$46.0M
APS ACTION Global Lead CoordinatorClinical and Translational Science CenterElena GkrouzmanNCATS NIH HHS UL1 TR000457NCATS NIH HHS UL1 TR001873
6 · The paper itself

Abstract

objectivesThis study focused on the prevalence and impact of ANA in aPL-positive patients without concomitant systemic autoimmune rheumatic diseases (SARDs).

methodsData from aPL-positive patients with or without Revised Sapporo APS classification criteria were retrieved from the Antiphospholipid Syndrome Alliance for Clinical Trials and International Networking (APS ACTION) Registry. Patients with concomitant SARDs were excluded.

resultsA total of 430 aPL-positive patients were included in the analysis, 56% ANA-positive (ANA+) and 44% ANA-negative (ANA-). ANA positivity was significantly associated with history of haematologic manifestations (persistent autoimmune haemolytic anaemia, thrombocytopenia, leukopenia and/or lymphopenia) (16% of ANA+ vs 7% of ANA-, P = 0.006). Triple aPL-positivity was more frequent in the ANA+ subgroup (P = 0.02), along with low baseline C3 and C4 levels (P = 0.05 and P = 0.009, respectively), and higher frequency for ENA. Among aPL-positive patients with no APS classification, ANA+ patients showed a higher rate of arthritis (P = 0.006). Among female patients who have experienced at least one pregnancy, 113 were ANA+ and 96 were ANA-; ANA- patients had a higher number of pregnancies (P = 0.018), and number of live births (P = 0.014). A wider proportion of ANA+ patients were treated with HCQ (P < 0.001).

conclusionWhen we analysed aPL-positive patients with no other SARDs, ANA status was not associated with thrombosis or pregnancy morbidity. Interestingly, ANA+ patients showed higher rates of systemic autoimmune features, including haematologic manifestations, multiple aPL positivity, lower complement levels, ENA positivity, and joint involvement, and were more often treated with HCQ. Finally, aPL-positive subjects who were ANA- had a higher rate of pregnancies and live births.

Indexed as

Antibodies, AntinuclearAntibodies, AntiphospholipidAntiphospholipid SyndromeAdultDatabases, FactualFemaleHumansMaleMiddle AgedPregnancyRegistriesAntibodies, AntinuclearAntibodies, Antiphospholipidantinuclear antibodiesantiphospholipid antibodiesantiphospholipid syndromephenotyping

Identifiers

PMID39423147
PMCPMC12225680

What OpenQuestion holds

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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.