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Thrombotic risk assessment in antiphospholipid syndrome: do noncriteria antibodies contribute?

dc.contributor.authorUludag, Omer
dc.contributor.authorCinar, Suzan
dc.contributor.authorMcDonnell, Thomas
dc.contributor.authorCene, Erhan
dc.contributor.authorYalcinkaya, Yasemin
dc.contributor.authorGul, Ahmet
dc.contributor.authorInanc, Murat
dc.contributor.authorArtim Esen, Bahar
dc.date.accessioned2026-06-27T15:07:30Z
dc.date.issued2023
dc.description.abstractBackground/aim: In this cross-sectional study, it was aimed to test the predictive value of noncriteria antiphospholipid antibodies (aPL) in addition to the global antiphospholipid syndrome score (GAPSS) in predicting vascular thrombosis (VT) in a cohort of patients with APS and aPL (+) systemic lupus erythematosus (SLE). Material and methods: This study included 50 patients with primary APS, 68 with SLE/APS, and 52 with aPL (+) SLE who were classified according to VT as VT +/- pregnancy morbidity (PM), PM only or aPL (+) SLE. Antiphospholipid serology consisting of lupus anticoagulant (LA), anticardiolipin (aCL) immunoglobulin G (IgG)/IgM/IgA, antibeta2 glycoprotein I (a(32GPI) IgG/IgM/IgA, antiphosphatidylserine/prothrombin (aPS/PT) IgG/IgM and antidomain-I (aDI) IgG was determined for each patient. The GAPSS and adjusted GAPSS (aGAPSS) were calculated for each patient, as previously defined. Logistic regression analysis was carried out with thrombosis as the dependent variable and high GAPSS, aCL IgA, a(32GPI IgA, and aDI IgG as independent variables. Results: The mean GAPSS and aGAPSS of the study population were 11.6 +/- 4.4 and 9.6 +/- 3.8. Both the VT +/- PM APS (n = 105) and PM only APS (n = 13) groups had significantly higher GAPSS and aGAPSS values compared to the aPL (+) SLE (n = 52) group. The patients with recurrent thrombosis had higher aGAPSS but not GAPSS than those with a single thrombotic event. The computed area under the receiver operating characteristic curve demonstrated that a GAPSS >= 13 and aGAPSS >= 10 had the best predictive values for thrombosis. Logistic regression analysis including a GAPSS >= 13, aCL IgA, a(32GPI IgA, and aDI IgG showed that none of the factors other than a GAPSS >= 13 could predict thrombosis. Conclusion: Both the GAPSS and aGAPSS successfully predict the thrombotic risk in aPL (+) patients and aCL IgA, a(32GPI IgA, and aDI IgG do not contribute to high a GAPSS or aGAPSS.en
dc.description.sponsorshipScientific Research Projects Coordination Unit of Idot
dc.description.sponsorshipstanbul University [TTU-2019-33932]
dc.description.urihttps://doi.org/10.55730/1300-0144.5671
dc.identifier.doi10.55730/1300-0144.5671
dc.identifier.eissn1303-6165
dc.identifier.endpage1074
dc.identifier.issn1300-0144
dc.identifier.issue5
dc.identifier.pubmed38813003
dc.identifier.startpage1067
dc.identifier.urihttps://hdl.handle.net/20.500.14981/68228
dc.identifier.volume53
dc.identifier.wos001108669900025
dc.language.isoeng
dc.publisherTubitak Scientific & Technological Research Council Turkey
dc.relation.ispartofTURKISH JOURNAL OF MEDICAL SCIENCES
dc.rightsopenAccess
dc.subjectAntiphospholipid syndrome
dc.subjectglobal antiphospholipid syndrome score
dc.subjectthrombotic risk
dc.subjectnon-criteria antiphospholipid antibodies
dc.subjectSYNDROME SCORE
dc.subjectCLASSIFICATION CRITERIA
dc.subjectDIAGNOSIS
dc.subjectMULTICENTER
dc.subjectVALIDATION
dc.subjectSTRATIFICATION
dc.subjectEVENT
dc.subjectGeneral & Internal Medicine
dc.titleThrombotic risk assessment in antiphospholipid syndrome: do noncriteria antibodies contribute?
dc.typeArticle
dspace.entity.typePublication
local.import.sourceWOS

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