Evidence map›Paper›PMID 37001919›Full record

ArticleRMD open2023

Triple positive profile in antiphospholipid syndrome: prognosis, relapse and management from a retrospective multicentre study.

Charlotte Laurent, Laure Ricard, Yann Nguyen, Jean Jacques Boffa, Eric Rondeau, Grigorios Gerotziafas, Ismail Elalamy, Sophie Deriaz, Claire De Moreuil, Virginie Planche and 4 more

Abstract readMulticenter Study
In one paragraph

Article in RMD open, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Machine learning for predicting thrombotic recurrence in antiphospholipid syndrome.Research and practice in thrombosis and haemostasis · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. 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

14 authors.

Charlotte LaurentSorbonne Université, AP-HP, Service de Médecine Interne and Inflammation-Immunopathology-Biotherapy Department (DMU i3), Hôpital Saint-Antoine, F-75012, Paris, France.
Laure RicardSorbonne Université, AP-HP, Service de Médecine Interne and Inflammation-Immunopathology-Biotherapy Department (DMU i3), Hôpital Saint-Antoine, F-75012, Paris, France.
Yann NguyenService de médecine médecine interne, AP-HP.Nord, Hôpital Beaujon, Université de Paris, Clichy, France.ORCID 0000-0002-0866-3824
Jean Jacques BoffaService de Néphrologie et dialyses, Hôpital Tenon, Paris, France.
Eric RondeauService des urgences néphrologiques et transplantation rénale, Hôpital Tenon, Paris, France.
Grigorios GerotziafasService d'hématologie biologique, Hôpital Tenon, Paris, France.
Ismail ElalamyService d'hématologie biologique, Hôpital Tenon, Paris, France.
Sophie DeriazService de médecine interne, Centre hospitalier et universitaire Bretonneau, Tours, France.
Claire De MoreuilService de médecine interne, Centre hospitalier et universitaire Brest, Brest, France.
Virginie PlancheSorbonne Université, Service de Hématologie biologique, AP-HP, Hôpital Saint-Antoine, 75012, Paris, France.
Cathererine JohanetImmunology Department, Saint-Antoine Hospital Assistance Publique-Hôpitaux de Paris (APHP), Paris, France.
Francois MillotService de médecine interne, Centre hospitalier et universitaire Bretonneau, Tours, France.
Olivier FainSorbonne Université, AP-HP, Service de Médecine Interne and Inflammation-Immunopathology-Biotherapy Department (DMU i3), Hôpital Saint-Antoine, F-75012, Paris, France.
Arsène MekinianSorbonne Université, AP-HP, Service de Médecine Interne and Inflammation-Immunopathology-Biotherapy Department (DMU i3), Hôpital Saint-Antoine, F-75012, Paris, France arsene.mekinian@aphp.fr.ORCID 0000-0003-2849-3049

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveAntiphospholipid syndrome (APS) is defined by the association of thromboembolic and/or obstetrical clinical manifestations and the presence of antiphospholipid antibodies. The objective of our study was to evaluate the impact of the triple-positive profile in a cohort of 204 APS patients.

methodsWe conducted a retrospective study, including patients with primary or secondary APS, meeting the Sydney criteria with at least one thrombotic and/or obstetrical complication. Clinical characteristics and the risk of relapse (defined by the occurrence of a new thrombotic event and/or a new adverse obstetrical event) between triple-positive and non-triple-positive APS patients were compared.

results204 patients were included in our study, 68 were triple-positive and 136 were single or double positive. 122 patients (59.8%) had primary APS. 67 patients (32.8%) had obstetrical APS, with a higher rate among triple-positive patients (45.6% vs 26.5%, p=0.010), and 170 patients (83.3%) had thrombotic APS, without difference between triple-positive and others. Thrombotic events were more often venous (56.4%) than arterial (37.7%). Triple-positive patients had more placental complications than others (17.6% vs 2.9%, p=0.001) and more non-criteria events (48.5% vs 25.7%, p=0.002). Among non-criteria events, there was a higher frequency of Sneddon syndrome in triple-positive patients (7.4% vs 0.7%, p=0.028). The relapse rate was higher in triple-positive patients than in others (63.2% vs 39,7%, p=0002). In multivariate analysis, the triple-positive profile was associated with a higher risk of relapse (HR 1.63; 95% CI 1.04 to 2.55; p=0.031).

conclusionThe triple-positivity is associated with a higher risk of relapse and obstetrical complications.

Indexed as

Antiphospholipid SyndromeThrombosisAntibodies, AntiphospholipidFemaleHumansPlacentaPregnancyPrognosisRetrospective StudiesAntibodies, Antiphospholipidantibodies, anticardiolipinantiphospholipid syndromeautoimmune diseases

Identifiers

PMID37001919
PMCPMC10069563

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.