Evidence map›Paper›PMID 33738987›Full record

ArticleACR open rheumatology2021

Beta-2-Glycoprotein-I Deficiency Could Precipitate an Antiphospholipid Syndrome-like Prothrombotic Situation in Patients With Coronavirus Disease 2019.

Manuel Serrano, Gerard Espinosa, Antonio Lalueza, Luz Yadira Bravo-Gallego, Raquel Diaz-Simón, Sara Garcinuño, Javier Gil-Etayo, Jorge Moises, Laura Naranjo, Sergio Prieto-González and 8 more

Open access · goldAbstract read
In one paragraph

Article in ACR open rheumatology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 3 pooled it
1.4field-weighted citation impact, top 16% 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

23 citing papers in PubMed, 3 syntheses or guidelines pooled it, 29 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Observational
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. COVID-19 and antiphospholipid antibodies.Best practice & research. Clinical haematology · 2022
    Review
  16. Observational
  17. Review
  18. Review
  19. Article
  20. 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

18 authors at 3 institutions in 1 country.

Manuel SerranoHospital 12 de Octubre, Healthcare Research Institute and Hospital Clínico San Carlos, Madrid, Spain.ORCID https://orcid.org/0000-0002-7177-667X
Gerard EspinosaHospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, University of Barcelona, Barcelona, Catalonia, Spain.ORCID https://orcid.org/0000-0003-1336-0163
Antonio LaluezaHospital 12 de Octubre, Healthcare Research Institute I+12, Madrid, Spain.ORCID https://orcid.org/0000-0003-2711-3817
Luz Yadira Bravo-GallegoHospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, University of Barcelona, Barcelona, Catalonia, Spain.
Raquel Diaz-SimónHospital 12 de Octubre, Healthcare Research Institute I+12, Madrid, Spain.
Sara GarcinuñoHospital 12 de Octubre, Healthcare Research Institute I+12, Madrid, Spain.
Javier Gil-EtayoHospital 12 de Octubre, Healthcare Research Institute I+12, Madrid, Spain.
Jorge MoisesHospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, University of Barcelona, Barcelona, Catalonia, Spain.
Laura NaranjoHospital 12 de Octubre, Healthcare Research Institute I+12, Madrid, Spain.
Sergio Prieto-GonzálezHospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, University of Barcelona, Barcelona, Catalonia, Spain.
Estibaliz Ruiz-OrtizHospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, University of Barcelona, Barcelona, Catalonia, Spain.
Beatriz SánchezHospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, University of Barcelona, Barcelona, Catalonia, Spain.
Ana Belen Moreno-CastañoHospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, University of Barcelona, Barcelona, Catalonia, Spain.
Carmen Díaz-PedrocheHospital 12 de Octubre, Healthcare Research Institute I+12, Madrid, Spain.
Odette Viñas-GomisHospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, University of Barcelona, Barcelona, Catalonia, Spain.
Ricard CerveraHospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, University of Barcelona, Barcelona, Catalonia, Spain.ORCID https://orcid.org/0000-0001-6085-492X
Antonio SerranoHospital 12 de Octubre, Healthcare Research Institute and Biomedical Research Centre Network for Epidemiology and Public Health, Madrid, Spain.ORCID https://orcid.org/0000-0003-1993-640X
APS-COVID 19 Study Group/European Forum on Antiphospholipid Antibodies
Universitat de Barcelona · ESResearch Institute Hospital 12 de Octubre · ESHospital Clínico San Carlos · ES

Funding

Institute of Health Carlos III. Spanish Ministry of Economy and Competitiveness co-funded with European Regional Development Fund. PI17/00147Institute of Health Carlos III. Spanish Ministry of Economy and Competitiveness co-funded with European Regional Development Fund. PI17/01129
6 · The paper itself

Abstract

objectivePatients with coronavirus disease 2019 (COVID-19) present coagulation abnormalities and thromboembolic events that resemble antiphospholipid syndrome (APS). This work has aimed to study the prevalence of APS-related antigens, antibodies, and immune complexes in patients with COVID-19 and their association with clinical events.

methodsA prospective study was conducted on 474 adults with severe acute respiratory syndrome coronavirus 2 infection hospitalized in two Spanish university hospitals. Patients were evaluated for classic and extra-criteria antiphospholipid antibodies (aPLs), immunoglobulin G (IgG)/immunoglobulin M (IgM) anticardiolipin, IgG/IgM/immunoglobulin A (IgA) anti-β2-glicoprotein-I (aβ2GPI), IgG/IgM antiphosphatidylserine/prothrombin (aPS/PT), the immune complex of IgA aβ2GPI (IgA-aβ2GPI), bounded to β2-glicoprotein-1 (β2GPI) and β2GPI levels soon after COVID-19 diagnosis and were followed-up until medical discharge or death.

resultsPrevalence of aPLs in patients with COVID-19 was as follows: classic aPLs, 5.8%; aPS/PT, 4.6%; IgA-aβ2GPI, 15%; and any aPL, 21%. When patients were compared with individuals of a control group of a similar age, the only significant difference found was the higher prevalence of IgA-aβ2GPI (odds ratio: 2.31; 95% confidence interval: 1.16-4.09). No significant differences were observed in survival, thrombosis, or ventilatory failure in aPL-positive versus aPL-negative patients. β2GPI median levels were much lower in patients with COVID-19 (15.9 mg/l) than in blood donors (168.8 mg/l; P < 0.001). Only 3.5% of patients with COVID-19 had normal levels of β2GPI (>85 mg/l). Low levels of β2GPI were significantly associated with ventilatory failure (P = 0.026).

conclusionβ2GPI levels were much lower in patients with COVID-19 than in healthy people. Low β2GPI-levels were associated with ventilatory failure. No differences were observed in the COVID-19 evolution between aPL-positive and aPL-negative patients. Functional β2GPI deficiency could trigger a clinical process similar to that seen in APS but in the absence of aPLs.

Identifiers

PMID33738987
PMCPMC8063141
OpenAlexW3137615388

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.